Skip to main content
Download PDF

Cholangiogenic potential of human deciduous pulp stem cell-converted hepatocyte-like cells

Stem Cell Research & Therapy volume 12, Article number: 57 (2021) Cite this article

Abstract

Background

Stem cells from human exfoliated deciduous teeth (SHED) have been reported to show the in vivo and in vitro hepatic differentiation, SHED-Heps; however, the cholangiogenic potency of SHED-Heps remains unclear. Here, we hypothesized that SHED-Heps contribute to the regeneration of intrahepatic bile duct system in chronic fibrotic liver.

Methods

SHED were induced into SHED-Heps under cytokine stimulation. SHED-Heps were intrasplenically transplanted into chronically CCl4-treated liver fibrosis model mice, followed by the analysis of donor integration and hepatobiliary metabolism in vivo. Immunohistochemical assay was examined for the regeneration of intrahepatic bile duct system in the recipient liver. Furthermore, SHED-Heps were induced under the stimulation of tumor necrosis factor alpha (TNFA).

Results

The intrasplenic transplantation of SHED-Heps into CCl4-treated mice showed that donor SHED-Heps behaved as human hepatocyte paraffin 1- and human albumin-expressing hepatocyte-like cells in situ and ameliorated CCl4-induced liver fibrosis. Of interest, the integrated SHED-Heps not only expressed biliary canaliculi ATP-binding cassette transporters including ABCB1, ABCB11, and ABCC2, but also recruited human keratin 19- (KRT19-) and KRT17-positive cells, which are considered donor-derived cholangiocytes, regenerating the intrahepatic bile duct system in the recipient liver. Furthermore, the stimulation of TNFA induced SHED-Heps into KRT7- and SRY-box 9-positive cells.

Conclusions

Collectively, our findings demonstrate that infused SHED-Heps showed cholangiogenic ability under the stimulation of TNFA in CCl4-damaged livers, resulting in the regeneration of biliary canaliculi and interlobular bile ducts in chronic fibrotic liver. Thus, the present findings suggest that SHED-Heps may be a novel source for the treatment of cholangiopathy.

Background

Orthotopic liver transplantation (OLT) is the only option to ameliorate liver refractory diseases, such as chronic liver fibrosis [1]. However, approximately 10% of patients with end-staged hepatic disorders are not able to receive the benefit owing to the extended waiting period and the shortage of donor organs [2, 3]. Human primary hepatocyte transplantation (hPHepT) becomes a considerable alternative to OLT, especially in liver-based inborn errors of hepatic metabolism and acute/fulminant liver failure [4,5,6]. Despite the clinical advantages of hPHepT, such as a less-invasive procedure, a current clinical limitation of clinical hPHepT is set by the shortage of effective donor hepatocytes and temporal efficacy [7].

Diverse human mesenchymal stem/stromal cell (MSC)-derived hepatocyte-like cells (HLCs) have been investigated as alternatives to hPHeps [8, 9]. Human deciduous pulp stem cells were first identified in the dental pulp tissues of exfoliated deciduous teeth, namely stem cells from human exfoliated deciduous teeth (SHED) [10], and are beneficial for the treatment of autoimmune, liver, and spinal injury diseases [11,12,13]. Recent studies demonstrated that SHED exhibit a hepatic potency under a sequential stimulation of hepatogenic cytokines, as referred to SHED-Heps, but SHED-Heps were immature and showed limited-function as hepatocytes [14, 15].

Chronic injury often causes ductular reaction in liver [16, 17]. Liver fibrosis is closely associated with the ductular reaction, resulting in bile excretion damage [18]. However, which therapeutic option regenerates intrahepatic bile ducts in cholestasis associated with liver diseases has yet not been elucidated. In this study, we investigated whether donor SHED-Heps recruited intrahepatic bile duct system, as well as reconstructed parenchymal hepatocytes, in fibrotic liver of chronically CCl4-treated mice. Further, we also investigated if SHED-Heps could be induced into cholangiocyte marker-expressing cells cultured under tumor necrosis factor alpha (TNFA) stimulation. Thus, this study aims to demonstrate our hypothesis of the cholangiogenic potency in vivo of SHED-Heps.

Methods

Mice

C57BL/6J mice (female, 6-week old) were purchased from Charles River Laboratories Japan (Yokohama, Japan). All animal experiments were approved by the Institutional Animal Care and Use Committee of Kyushu University (approval no. A21-044-1 and A20-041-0). All animals were housed in temperature- and light-controlled conditions with a 12-h light and dark cycle, and fed water and standard pellet chow ad libitum.

Antibodies

Additional file 1 Supplementary Table 1 lists the antibodies used in this study.

Isolating, culturing, and characterizing SHED and generating SHED-Heps

SHED were isolated, cultured, and characterized according to previous studies [10, 11] (Additional file 1: Supplementary Fig. 1). The details of SHED culture procedures are as described in the Additional file 1: Supplementary Methods.

Induction of SHED-Heps

P3 SHED were seeded at 2.5 × 105 cells per dish on human fibronectin-coated 100-mm culture dishes (Corning) and maintained in a growth medium. After they reached confluency, SHED were treated with epidermal growth factor (EGF; 20 ng/mL; PeproTech, Rocky Hill, NJ) and fibroblast growth factor 2 (FGF2; 10 ng/mL; PeproTech) in Iscove’s modified Dulbecco’s media (IMDM; Thermo Fisher Scientific, Waltham, MA) and premixed antibiotics of 100 U/ml penicillin and 100 μg/ml streptomycin (premixed P/S antibiotics; Nacalai Tesque, Kyoto, Japan) for 2 days [14, 19] (Supplementary Fig. S2a). Subsequently, the cells were cultured using hepatogenic cytokines and regents. Initially, the cells were stimulated with FGF2 (10 ng/mL; PeproTech), hepatocyte growth factor (HGF; 20 ng/mL; PeproTech), and nicotinamide (0.61 g/L; Merck, Darmstadt, Germany) in IMDM (Thermo Fisher Scientific) and premixed P/S antibiotics (Nacalai Tesque) for 7 days. Finally, they were stimulated with oncostatin M (20 ng/mL; PeproTech), dexamethasone (1 μM; Merck), insulin-transferrin-selenium premix solution (ITS) premix (1×; Corning), and premixed P/S antibiotics (Nacalai Tesque) for 21 days. Each medium was changed twice weekly. The generated SHED-Heps were re-seeded at 0.1 × 106 per well in low cell attachment PrimeSurface 96 U multiwell plates (Sumitomo Bakelite, Tokyo, Japan). The medium contained oncostatin M (20 ng/mL; Pepro Tech), dexamethasone (1 mM; Merck), ITS premix (1×; Thermo Fisher Scientific), and premixed P/S antibiotics (Nacalai Tesque) in IMDM (Thermo Fisher Scientific) for 7 days, as described previously [15].

Transplantation of SHED-Heps (SHED-HepT) into CCl4-treated chronic liver fibrosis model mice

A CCl4 solution in olive oil (1.0 mL/kg body weight; CCl4 to olive oil = 1:4 volume/volume; Wako Pure Chemicals, Osaka, Japan) was intraperitoneally injected into C57BL/6J mice twice a week for 8 weeks, as described previously [12, 19]. Age-matched C57BL/6J mice infused with olive oil (Wako Pure Chemicals) were used as controls. The generated SHED-Heps were washed with sterilized with phosphate-buffered saline and kept in cold phosphate-buffered saline (PBS) on ice and quickly infused into the recipient spleen within 10 min after the preparation to maintain the initially prepared donor cell viability. Four-week-CCl4-treated C57BL/6J mice were intrasplenically infused SHED-Heps (1 × 106/10 g body weight in 100 μL of PBS). Age-matched 4-week-CCl4-treated C57BL/6J mice were infused with PBS (100 μL) as experimental controls. All mice did not receive any immunosuppressants throughout the experiment.

In vivo monitoring of transplanted donor cells

SHED-Heps were labeled with XenoLight DiR NIR Fluorescent Dye (DiR; 10 μg/mL; Perkin Elmer, Waltham, MA) for 30 min at 37 °C. The DiR-labeled cells or non-labeled SHED-Heps (each 1 × 106 in 100 μL of PBS) were intrasplenically infused into 4-week-CCl4-treated C57BL/6J mice. Ventral images of the mice were obtained 24 h after infusion with an optical in vivo imaging system IVIS Lumina III (Perkin Elmer) using living image software (Perkin Elmer).

Isolation of whole liver cells (WLCs) from recipient CCl4-treated mice

Mouse livers were perfused with Liver Perfusion Medium (Thermo Fisher Scientific) at 37 °C for 5 min through the vena cava, followed by 0.1% collagenase type I (Worthington Biochemicals, Lakewood, NJ) at 37 °C for 15 min. The liver samples were gently loosened, and WLCs were obtained through a 70-μm cell strainer.

Histological assays of mouse liver tissues

Tissue samples were fixed with formalin and embedded in paraffin. The paraffin sections were used for immunohistochemical and double immunofluorescent analyses, as described in the Additional file 1: Supplementary Methods, previously [11, 14]. The primary antibodies used in immunohistochemical and immunofluorescent assays are summarized in the Additional file 1: Supplementary Table 2. Immunohistochemical and immunofluorescent controls were treated with isotype-matched antibodies instead of primary antibodies. Paraffin sections of normal human and mouse liver tissues were stained with the primary antibodies and examined for cross-reactivity of the primary antibodies. Several paraffin sections were treated with hematoxylin and eosin staining.

In vivo bile assay

Total bilirubin in mouse serum was measured by colorimetric assay using Bilirubin QuantiChrom Assay Kit (BioAssay Systems, Hayward, CA) according to the manufacturer’s instructions. Human albumin (ALB) in mouse serum was analyzed by enzyme-linked immunosorbent assay (ELISA) using human albumin ELISA Quantitation set (Behtyl Laboratory, Montgomery, TX). Feces were collected after fasting overnight. Bile acid in feces was measured by colorimetric assay using Total Bile Acid-Test Wako (Wako Pure Chemical).

In vivo biliary secretion assay

C57BL/6J mice were intravenously infused with cholyl-lysyl-fluorescein (CLF; 1 mM, 100 μL; Corning, Corning, NY) and harvested 2 h after injection. The amount of CLF in the liver, serum, and urine was quantitated by measuring fluorescence, as described previously [20].

In vitro biliary function assay

Gene expression of uridine 5′-diphospho-glucuronosyltransferase 1A1 (UGT1A1), membrane metalloendopeptidase (MME), ATP-binding cassette transporter B1 (ABCB1), ABC11, and ABCC2 was analyzed in SHED-Heps by reverse transcription-quantitative polymerase chain reaction (RT-qPCR), as described in the Additional file 1: Supplementary Methods. Distribution of MME, ABCB1, ABCB11, and ABCC2 in SHED-Hep spheroids was analyzed by immunohistochemistry. To analyze hepatobiliary function assays, SHED-Heps were incubated with indirect bilirubin (25 μM; Merck, Darmstadt, Germany) in Ca2+-free HBSS (Nacalai Tesque) at 37 °C for 60 min and used for determining direct bilirubin by colorimetric assay using QuantiChrom Bilirubin Assay Kit (BioAssay Systems) according to the manufacturer’s instructions. SHED-Heps were also incubated with CLF (5 μM; Corning) in Ca2+-free Hank’s balanced salt solution (HBSS; Nacalai Tesque) at 37 °C for 15 min. Intact SHED and human intrahepatic biliary epithelial cells (AXOL, Cambridge, UK) were used as controls.

Immunophenotype analysis of SHED-Heps and WLCs

The expression of CD90, epithelial cell adhesion molecule (EPCAM), promin-1 (PROM1), MME, CD146, and CD34 were analyzed in SHED-Heps and WLCs by flow cytometric (FCM) analysis, as described in the Additional file 1: Supplementary Methods.

Induction of SHED-Heps into cholangiocyte marker-expressing cells

SHED-Heps were maintained in William’s medium E (Thermo Fisher Scientific) and premixed P/S antibiotics (Nacalai Tasque) supplemented with or without TNFA (20 ng/mL; PeproTech) for 4 days. Gene expression of human hepatocyte nuclear factor 6 (HNF6), human SRY-box 9 (SOX9), human cytokeratin 7 (KRT7), and human KRT19 was analyzed by RT-qPCR. The distribution of human SOX9, human KRT7, and human ALB was analyzed by immunofluorescence, as described in the Additional file 1: Supplementary Methods.

Statistical analysis

Statistical results were expressed as means ± standard deviation (SEM) from, at least, triplicate measurements. Comparisons between two groups were analyzed by independent two-tailed Student’s t tests. Multiple group comparison was analyzed by one-way repeated measures analysis of variance followed by the Tukey post hoc test. The values of P < 0.05 were considered statistically significant. All statistical analyses were performed using PRISM 6 software (GraphPad, Software, La Jolla, CA).

Results

SHED are induced to hepatocyte-lineage committed cells in vitro

We isolated SHED with a criteria of MSCs, including attached colony formation, cell surface antigen expression, and multipotency into osteoblasts, chondrocytes, and adipocytes [21] (Additional file 1: Supplementary Fig. 1). We cultured SHED under a hepatogenic condition (Additional file 1: Supplementary Fig. 2a). We found a morphological change of spindle-shaped intact SHED into hexagonal-shaped SHED-Heps and bile canaliculi-like structures intercellular space of SHED-Heps under the hepatogenic condition (Additional file 1: Supplementary Fig. 2b). RT-qPCR showed that SHED-Heps expressed higher levels for KRT18, ALB, transthyretin (TTR), HNF1A, HNF4A, nuclear receptor subfamily 1 group I member 2 (NR1I2), and peroxisome proliferator activated receptor alpha (PPARA) than intact SHED, but lower in SHED-Heps than in hPHeps; meanwhile, SHED-Heps and intact SHED did not express alpha fetoprotein (AFP), but hPHeps expressed (Additional file 1: Supplementary Fig. 2c). Immunohistochemical analysis detected ALB in SHED-Heps, but not in SHED (Additional file 1: Supplementary Figs. 2d). SHED-Heps showed higher levels of various hepatocyte-specific genes, which are related to urea cycle, glycogen, amino acid, lipid metabolism, xenobiotics, and production of coagulation factor, than intact SHED, but lower than hPHeps by RT-qPCR (Additional file 1: Supplementary Fig. 3).

SHED-Heps exhibited the increased release of glucose, triglyceride, ALB, and fibrinogen, but not AFP into the CM, the decreased ammonia in the CM, the increased intracellular urea, and the enhanced activity of cytochrome P450 3A4 compared to intact SHED (Additional file 1: Supplementary Figs. 4a–4e). SHED-Heps showed the ability of different metabolites storage including indocyanine green uptake and release after 6 h, cytoplasmic accumulation of acetylated low-density lipoprotein uptake, and glycogen storage, but intact SHED did not exhibit any storage function (Additional file 1: Supplementary Figs. 4f–4i). The functions were lower in SHED-Heps than in hPHeps (Additional file 1: Supplementary Fig. 4), indicating that SHED-Heps were immature and limited-functional hepatic committed cells.

SHED-HepT ameliorates liver fibrosis in chronically CCl4-treated mice

Four-week-CCl4-treated C57BL/6J mice were intrasplenically infused SHED-Heps (1 × 106 per mouse) and subsequently received CCl4 for 4 weeks after transplantation (Fig. 1a). Biochemical assays showed the reduced serum levels of aspartate aminotransferase and alanine aminotransferase in recipient mice 4 weeks after transplantation (Additional file 1: Supplementary Fig. 5a). The liver fibrosis was reduced by SHED-HepT, as indicated by the reduced levels of hydroxyproline content, collagen type I mRNA expression, fibrous tissue deposition, and fibrosis score by biochemical analysis, RT-qPCR, Masson Trichrome staining, and Ishak scoring (Additional file 1: Supplementary Figs. 5b–5e). Fibrous rates were 0.39% ± 0.63% (means ± SEM) in the control non-treated liver, 4.29% ± 2.51% in the CCl4-treated liver, and 0.91% ± 0.41% in the SHED-Hep-transplanted CCl4-treated liver 4 weeks after transplantation by Masson Trichrome staining. SHED-HepT showed the decreased levels of alpha-smooth muscle actin 2, smooth muscle, aorta (ACTA2)-positive cells and fibrogenesis-related marker genes for Acta2, matrix metalloprotease 2, transforming growth factor beta, and TNFA in the recipient liver by immunohistochemical analysis and RT-qPCR (Additional file 1: Supplementary Figs. 5f, 5 g).

Fig. 1
figure 1

Transplanted donor SHED-Heps engraft without cell fusion in livers of recipient CCl4-treated mice. a A schema of SHED-Hep transplantation (SHED-HepT) into chronically CCl4-treated mice. Mice were intraperitoneally treated with CCl4 (1 mg/kg in olive oil, red arrowheads) twice a week for 8 weeks and administrated SHED-Heps (1.0 × 106/mouse) 4 weeks after CCl4 treatment. The mice were harvested 8 weeks after CCl4 treatment. b Representative images of in vivo kinetics of donor SHED-Heps were detected in CCl4-treated mice 24 h after SHED-HepT by DiR labeling. c–i Distribution of donor SHED-Heps was analyzed in the livers 4 weeks after the transplantation. Representative histogram of human leucocyte antigens A, B, and C (HLA-ABC) expression in the recipient whole liver cells (WLCs) by flow cytometric (FCM) assay. Area filled with red: target antibody-stained histograms; solid line: isotype-matched control-stained histograms. Number indicates averages of the positive rate (c). Representative images of HLA-ABC (d), hepatocyte paraffin 1 antigen (HepPar1; e), and human albumin (hALB; f) were detected by immunohistochemical analysis. Serum levels of hALB by enzyme-linked immunosorbent assay (ELISA). n = 5. nd, no detection. The graph bars represent the means ± standard error of mean (SEM) (g). Representative images of the expression of HepPar1 and hALB (h) and HepPar1 and mouse albumin (mALB, i) were detected by double immunofluorescent analysis. Nuclei were stained with 4′,6-diamidino-2-phenylindole (DAPI). Merge: merged image. b, d–i: Cont, olive oil-treated mice; CCl4, CCl4-treated mice; SHED-Hep, SHED-Hep-transplanted CCl4-treated mice. d–f, h, i: Scale bars, 50 μm (d–f) and 10 μm (h, i)

Full size image

Transplanted donor SHED-Heps integrate in liver tissue of chronically CCl4-treated mice

In vivo cell tracking analysis showed that fluorescent intensity was detected on the recipient body corresponding to the liver 24 h after DiR-labeled SHED-HepT, but not on control mouse body (Fig. 1b). FCM analysis showed the expression of a ubiquitous human cell marker, human leukocyte antigens A, B, and C (HLA-ABC) on WLCs isolated from the recipient mice 4 weeks after transplantation (Fig. 1c). Immunohistochemical analysis using human-specific antibodies showed that HLA-ABC-, human hepatocyte-specific hepatocyte paraffin 1- (HepPar1-), and human ALB-positive cells were detected in the liver parenchymal periphery of recipient mice (Fig. 1d–f). No signal was detected on human and mouse liver tissues by immunohistochemical control tests using isotype-matched antibodies instead of the human-specific antibodies (Additional file 1: Supplementary Fig. 6). Antibody cross-reactivity test evaluated the human specificity of HLA-ABC, HepPar1, and human ALB antibodies, but not the mouse specificity on human and mouse liver tissues (Additional file 1: Supplementary Figs. 7a–7c). Homing rates of HepPar1-positive area were 3.31% ± 1.63% in SHED-Hep-transplanted group, but not detected in both non-treated and CCl4-treated groups. By ELISA, serum human ALB was detected in SHED-Hep-transplanted mice, but not in non-treated and CCl4-treated mice (Fig. 1g). By double immunofluorescent analysis, HepPar1-positive cells co-expressed human ALB, but not mouse ALB, in the liver parenchyma of recipient mice (Fig. 1h, i).

SHED-HepT rescues biliary excretion in chronically CCl4-treated mice

CCl4 treatment caused cholestasis in mice, as indicated by the increased levels of serous total bilirubin, the decreased levels of fecal bile acid, and the increased amounts of serous and hepatic CLF by biochemical and biliary excretion analyses (Fig. 2a–c). SHED-HepT recovered the levels of serous total bilirubin and fecal bile acid and the amounts of serous and hepatic CLF 4 weeks after transplantation (Fig. 2a–c). No urinary CLF was found in all experimental groups (Fig. 2c). Histological analysis showed that chronic CCl4 treatment damaged biliary canaliculi and interlobular bile ducts in the parenchymal periphery and periportal region of mouse liver; meanwhile, SHED-HepT regenerated the CCl4-damaged biliary canaliculi and interlobular bile ducts (Fig. 2d).

Fig. 2
figure 2

SHED-HepT rescues biliary excretion in recipient CCl4-treated mice. a, b Levels of serum total bilirubin (a) and fecal bile acid (b) 4 weeks after transplantation by colorimetry. c Cholyl-L-lysyl-fluorescein (CLF) was intravenously infused into mice. The graphs showed the amount of CLF in serum, urine, and liver 2 h after the infusion. d–h Liver tissues were analyzed 4 weeks after SHED-HepT. Representative images of the livers were obtained by hematoxylin and eosin (H&E) staining (d) and by immunohistochemical analysis using human-specific antibodies to membrane metalloendopeptidase (MME; e, f), keratin 19 (KRT19; g), and KRT7 (KRT7; h). Nuclei were stained with hematoxylin. a–c n = 5 for all groups. **P < 0.01, ***P < 0.005. nd, no detection; ns, no significance. The graph bars represented the means ± SEM. d arrow: bile duct. d–h Scale bars, 20 μm (d, f-h) and 50 μm (e). d, f–h PV, portal vein

Full size image

MME is a pan marker for bile canaliculi. We then demonstrated that the reactivity of MME was reduced in the liver parenchymal periphery of CCl4-treated mice compared to that of control mice by immunohistochemical analysis using anti-human MME antibody (Fig. 2e, Additional file 1: Supplementary Figs. 7d, 8). Interestingly, SHED-HepT increased the MME reactivity in recipient liver (Fig. 2e, Additional file 1: Supplementary Fig. 8). ABCB1, ABCB11, and ABCC2 are bile canaliculi-specific hepatobiliary transporters to excrete bile from hetatocytes into bile canaliculi [22,23,24,25]. We showed that ABCB1, ABCB11, and ABCC2 were abundantly expressed in the liver parenchymal periphery of SHED-Hep-transplanted CCl4-treated mice compared to that in control CCl4-treated mice by immunohistochemical analysis using the corresponding human-specific antibodies (Additional file 1: Supplementary Fig. 9). Immunohistochemical cross-reactivity and control tests determined that the present anti-ABCC2 antibody showed the human specificity; meanwhile, the anti-ABCB1, anti-ABCB11, and anti-MME antibodies did not (Additional file 1: Supplementary Figs. 6, 7d, 9). Double immunofluorescent analysis showed that HepPar1-positive cells co-expressed, at least partially, ABCB1, ABCB11, and ABCC2, as well as MME, in the recipient liver parenchyma (Additional file 1: Supplementary Fig. 10).

Immunohistochemical analysis using anti-human MME antibody showed MME-positive signals in liver interlobular bile ducts of SHED-Hep transplanted mice, but not in those of CCl4-treated mice (Fig. 2f). We then performed immunohistochemical analysis using anti-mouse KRT19, anti-human KRT19, and anti-human KRT7 antibodies. Mouse KRT19 immunoreactivity was not detected in the liver tissue of CCl4-treated mice; meanwhile, it was found in liver interlobular bile ducts of control mice (Additional file 1: Supplementary Fig. 11a). Human KRT19 and human KRT7 immunoreactivity were detected in liver interlobular bile ducts of SHED-Hep transplanted mice, but not in that of control and CCl4-treated mice (Fig. 2g, h, Additional file 1: Supplementary Figs. 11b, 11c). Immunohistochemical cross-reactivity and control tests evaluated human cholangiocyte specificity of anti-human KRT7 and anti-human KRT19 antibodies, as well as mouse cholangiocyte specificity of anti-mouse KRT19 antibody (Additional file 1: Supplementary Fig. 7, 11).

SHED-Heps exhibit cholangiogenic potency under TNFΑ stimulation in vitro

SHED-Heps expressed UGT1A1 by RT-qPCR and exhibited the production of direct bilirubin and the function of hepatobiliary transport by colorimetric assay and CLF staining (Fig. 3a–c). RT-qPCR and immunohistochemical analysis demonstrated the gene and protein expression of hepatobiliary transporters, including MME, ABCB1, ABCB11, and ABCC2 in SHED-Heps (Fig. 3d, e). Meanwhile, intact SHED did not show the hepatobiliary ability (Fig. 3a–e). Further FCM analysis revealed that SHED-Heps expressed hepatic markers, CD90 and MME, but did not express critical hepatic progenitor cells (HPCs) markers, EPCAM, PROM1, and neural cell adhesion molecule 1 (NCAM1) [26, 27] (Fig. 3f). SHED-Heps did not also express CD146, which is considered as a critical and primitive marker for MSCs [28], and definitive hematopoietic marker CD34 by FCM analysis (Fig. 3f). Next, we examined the immunophenotype of WLCs isolated from SHED-Hep-transplanted mice by FCM analysis using human-specific antibodies to CD90, MME, EPCAM, PROM1, NCAM1, CD146, and CD34. Of interest, WLCs expressed human EPCAM, human PROM1, human NCAM1, and human CD146, as well as human CD90 and human MME, but not human CD34 (Fig. 3g), implying that the recipient liver environment may induce donor SHED-Heps into cholangiocytes or cholangiocyte-progenitor cells (CPCs).

Fig.3
figure 3

SHED-HepT reconstructs intrahepatic bile ducts in livers of recipient CCl4-treated mice. a–e In vitro hepatobiliary function was analyzed in SHED-Heps. Gene expression of uridine 5′-diphospho-glucuronosyltransferase 1A1 (UGT1A1) by reverse transcription-quantitative polymerase chain reaction (RT-qPCR). Amount of direct bilirubin by colorimetric assay (b). Representative images of bile transport were detected by CLF staining. Nuclei were stained with DAPI (c). Gene expression of membrane metalloendopeptidase (MME), ATP-binding cassette transporter B1 (ABCB1), ABCB11, and ABCC2 by RT-qPCR d. Representative images of the expression of MME, ABCB1, ABCB11, and ABCC2 were detected by immunohistochemical analysis (e). a–e hPHep, human primary hepatocyte. a, b, d n = 5 for all groups. ***P < 0.005. nd, no detection. The graph bars represent the means ± SEM. a, d Results are shown as a ratio to hPHeps (hPHep = 1). c, e Scale bars, 20 μm. f, g Representative histograms of the expression of cell surface markers for hepatocyte progenitors and mesenchymal stem cells in SHED-Heps (f) and whole liver cells isolated from recipient mice (WLC) (g) were detected by FCM assay. EPCAM: epithelial cell adhesion molecule; MME: membrane metalloendopeptidase; NCAM1: neural cell adhesion molecule; PROM1: promin 1; R-PE: R-phycoerythrin. f Red solid line, target antibody-stained histograms; black solid line, isotype-matched control-stained histograms. g Area filed with red, target antibody-stained histograms; solid line, isotype-matched control-stained histograms

Full size image

TNFA can induce hepatocytes into bile ductular cells [29]. The present and previous [12] studies showed that chronic CCl4 treatment enhances abundant TNFA expression in mouse liver tissue. SHED-Heps were maintained in William’s E medium stimulated with or without TNFA for 4 days (Fig. 4a). The culture conditions, especially TNFA-co-stimulating condition, enhanced the expression of HNF6, SOX9, and KRT7 in SHED-Heps by RT-qPCR (Fig. 4b) and the expression of SOX9 and KRT7, but not human ALB, by immunofluorescent analysis (Fig. 4c–e).

Fig. 4
figure 4

SHED-Heps exhibit a potency into cholangiocyte-like cells. a A schema of induction of SHED-Heps into cholangiocyte-like cells (SHED-Chols). Generated SHED-Heps were cultured in William’s medium (WEM) with or without tumor necrosis factor alpha (TNFA +/−) for 4 days. Dex: dexamethasone; EGF: epidermal growth factor; FGF2: fibroblast growth factor 2; HGF: hepatocyte growth factor; IMDM: Iscove’s modified Dulbecco’s medium; ITS: insulin-transferrin-selenium premix solution; NCA: nicotinamide; OSM: oncostatin M. b Gene expression of hepatocyte nuclear factor6 (HNF6), SRY-box 9 (SOX9), KRT7, and KRT19 by RT-qPCR analysis. Results are shown as a ratio to human primary cholangiocyte (hChol = 1). n = 5 for all groups. *P < 0.05, ***P < 0.005. nd, no detection; ns, no significance. The graph bars represent the means ± SEM. c–e Representative images of SOX9, KRT7, and ALB expression were detected by immunofluorescent assay. Nuclei were stained with DAPI. Merge, merged image. Scale bars, 20 μm. b–e SHED-Chol−, TNFA-non-stimulated group; SHED-Chol+, TNFA-stimulated group

Full size image

Discussion

Here, we demonstrated that the donor SHED-Heps integrate into liver parenchyma, in recipient chronically CCl4-damaged mice, and regenerate the intrahepatic biliary components. Hepatic damages due to liver fibrosis reduce and lack the distribution of MME in bile canaliculi [30]. Bile canalicular transporters ABCB1, ABCB11, and ABCC2 are defected in congenital cholestasis, including progressive familial intrahepatic cholestasis type2, benign recurrent intrahepatic cholestasis type2, and Dubin Johnson syndrome [31,32,33]. HPCs are responsible for developing CPCs and cholangiocytes [26]. Hepatocytes exhibit plasticity to recruit bile ductular cells under liver physiological and pathological conditions [34]. Transplanted hepatocytes can differentiate into bile ductular cells in bile duct ligation model animals [35]. A recent study showed that mature hepatocytes undergo the in situ potency of direct differentiation into SOX9-expressing CPCs through HPCs with mesenchymal phenotype [36]. In this study, WLCs from SHED-Hep-transplanted mice contained SHED-derived HPCs and MSCs, but donor SHED-Heps did not contain HPCs and MSCs. The present study showed that integrated SHED-Heps rescued the expression of MME, ABCB1, ABCB11, and ABCC2 in bile canaliculi under chronically CCl4-damaged environment. These findings imply a plastic possibility of SHED-Heps to commit to CPCs/cholangiocytes through HPCs in situ and suggest that SHED-Heps might be a source for treating cholestasis associated with bile canaliculi.

Although we revealed that transplanted SHED-Heps recruited bile ductular cells in the recipient livers, the mechanism(s) of SHED-Hep into bile ductular cells remains unknown. Epithelial-mesenchymal transition (EMT) enables mature epithelial cells to undergo transdifferentiation into mesenchymal cells acquired with stem cell-like properties in chronically inflamed tissue [37]. TNFA accelerates EMT via the nuclear factor kappa B–Twist pathway in mammary epithelial cells [38]. Moreover, TNFA can induce the differentiation of hepatocytes into cholangiocytes in organoid culture system [29]. In this study, TNFA enhanced the expression of SOX9 and KRT7 in SHED-Heps. These findings suggest that the inflammatory background by CCl4, such as TNFA, may recruit donor SHED-Heps into CPC/cholangiocyte-like cells through HPC state. Further studies will be required to evaluate the molecular mechanisms in TNFA-triggered cholangiocyte-differentiation of SHED-Hep for treating cholangiopathy.

In the present and recent animal studies [12], both systemically transplanted SHED and SHED-Heps recovered chronically CCl4-treated liver fibrosis. Meanwhile, systemically transplanted SHED-Heps, but not SHED, rescued Wilson’s disease disorders [14]. Local implantation of SHED-Hep-aggregates gives a benefit for Factor VIII-lacked Hemophilia A [15]. These findings suggest that diverse approaches using SHED and SHED-Heps give an advantage for treating liver disease. A standard operating procedure (SOP) for manufacturing clinical-grade cell products should be validated before clinical applications [39]. Therefore, currently validated SOP for manufacturing large-scale clinical-grade SHED products [25] might be useful to establish safety-secured and clinical-graded SHED-Hep products. More research will be necessary to improve the quality and safety of SHED-Heps, such as microbial contamination, chromosomal instability, immunogenicity, and tumorigenicity [40]. Post-cryopreserved viability and function of clinical-grade SHED-Hep products should be needed for transplantation [41], because freeze-thawing process reduces the viability and function of donor hepatocytes due to the damage of mitochondrial respiration [42].

In this study, the long-term survival and engraftment of SHED-Heps were not investigated. In a recent study in Wilsons’ disease model animal [14], the long-term survival and engraftment of SHED-Heps are not expected. The reasons why SHED-Heps exhibit the short-term survival and engraftment in the recipient animals are considered due to the immature hepatic differentiation and immunogenicity of donor cells, the xenograft system in immunocompetent animals without any immunosuppressive drug, and the chronical cytotoxic condition after transplantation. On the other hand, SHED-secreting trophic factors including cytokines and extracellular vesicle-containing RNA contents affect immunosuppressive functions [43, 44]. The effect of stanniocalcin 1 secreted from SHED-Heps is anti-hepatitis [14]. Given the results from SHED-Heps transplantation in the intoxicated mice, anti-inflammatory effects by SHED-secreting factors may support the regeneration of bile ducts.

In vivo cell fusion with recipient hepatocyte has been considered as a mechanism to integrate donor cells, such as bone marrow hematopoietic cells and hematopoietic cell-derived hepatocytes, in fumarylacetoacetate hydrolase-deficient immunodeficient and chronic CCl4-treated immunocompetent mice [45, 46]. Meanwhile, only bone marrow MSCs can integrated without cell fusion with recipient hepatocytes in the damaged liver [47]. We evaluated that donor SHED can integrate as human HLCs without cell fusion with recipient hepatocytes [12]. Given the present results from fusion failure of donor SHED-Heps, SHED and SHED-Heps may exhibit a unique process to integrate in the recipient damaged liver in vivo. The present hepatic culture system using growth factors and hormones at specific times and in a specific sequence was insufficient to induce SHED into mature and functional HLCs. Based on a recent study, stem cells need to drive them through primitive steak under the stimulation of both inductive and repressive signals for developing into mature and functional hepatocytes [48]. The primitive steak is a critical stage of mimicking developmental biology in an in vitro system, because only the primitive steak can drive definitive endoderm, progenitors, hepatoblasts, and finally mature hepatocytes. Further studies will be necessary to evaluate the in vivo and in vitro mechanism of SHED into mature hepatocytes and cholangiocytes.

Conclusions

Collectively, SHED-Heps integrate into liver parenchyma, especially its periphery, in recipient chronically CCl4-damaged mice and contributes to the regeneration of intrahepatic bile ducts under fibrosis-associated TNFA microenvironment. Thus, SHED-Heps might be a source for treating cholestasis associated with bile canaliculi.

Availability of data and materials

All data generated and analyzed during this study are included in this published article and its supplementary information files.

Abbreviations

ABCB1:

ATP-binding cassette transporter B1

ABCB11:

ATP-binding cassette transporter B11

ABCC2:

ATP-binding cassette transporter C2

AFP:

Alpha fetoprotein

ACTA2:

Alpha-smooth muscle actin 2, smooth muscle, aorta

ALB:

Albumin

CLF:

Cholyl-lysyl-fluorescein

CPCs:

Cholangiocyte-progenitor cells

EGF:

Epidermal growth factor

ELISA:

Enzyme-linked immunosorbent assay

EMT:

Epithelial-mesenchymal transition

EPCAM:

Epithelial cell adhesion molecule

FCM:

Flow cytometry

FGF2:

Fibroblast growth factor 2

HBSS:

Hank’s balanced salt solution

HepPar1:

Hepatocyte paraffin 1

HGF:

Hepatocyte growth factor

HLA-ABC:

Human leukocyte antigens A, B, and C

HLCs:

Hepatocyte-like cells

HNF1A:

Hepatocyte nuclear factor 1A

HNF6:

Hepatocyte nuclear factor 6

HPCs:

Hepatic progenitor cells

hPHeps:

Human primary hepatocytes

IMDM:

Iscove’s modified Dulbecco’s media

ITS:

Insulin-transferrin-selenium premix solution

KRT7:

Cytokeratin 7

KRT18:

Cytokeratin 18

KRT19:

Cytokeratin 19

MME:

Membrane metalloendopeptidase

MSCs:

Mesenchymal stem/stromal cells

NCAM1:

Neural cell adhesion molecule 1

NR1I2:

Nuclear receptor subfamily 1 group I member 2

PBS:

Phosphate-buffered saline

PPARA:

Peroxisome proliferator activated receptor alpha

PROM1:

Promin-1

RT-qPCR:

Quantitative reverse transcription and polymerase chain reaction

SHED:

Stem cells from human exfoliated deciduous teeth

SHED-Heps:

SHED-derived hepatocyte-like cells

SOP:

Standard operating procedure

SOX9:

SRY-box 9

TNFA:

Tumor necrosis factor alpha

TTR:

Transthyretin

UGT1A1:

5′-Diphospho-glucuronosyltransferase 1A1

WLCs:

Whole liver cells

References

  1. Sze YK, Dhawan A, Taylor RM, Bansal S, Mieli-Vergani G, Rela M, et al. Pediatric liver transplantation for metabolic liver disease: experience at King’s College Hospital. Transplantation. 2009;87:87–93.

    Article  PubMed  Google Scholar 

  2. Murray KF, Carithers RL. AASLD practice guidelines: evaluation of the patient for liver transplantation. Hepatology. 2005;41:1407–32.

    Article  PubMed  Google Scholar 

  3. Kim WR, Therneau TM, Benson JT, Kremers WK, Rosen CB, Gores GJ, et al. Deaths on the liver transplant waiting list: an analysis of competing risks. Hepatology. 2006;43:345–51.

    Article  CAS  PubMed  Google Scholar 

  4. Fox IJ, Chowdhury JR, Kaufman SS, Goertzen TC, Chowdhury NR, Warkentin PI, et al. Treatment of the Crigler–Najjar syndrome type I with hepatocyte transplantation. N Engl J Med. 1998;338:1422–7.

    Article  CAS  PubMed  Google Scholar 

  5. Muraca M, Gerunda G, Neri D, Vilei MT, Granato A, Feltracco P, et al. Hepatocyte transplantation as a treatment for glycogen storage disease type 1a. Lancet. 2002;359:317–8.

    Article  PubMed  Google Scholar 

  6. Dhawan A, Puppi J, Hughes RD, Mitry RR. Human hepatocyte transplantation: current experience and future challenges. Nat Rev Gastroenterol Hepatol. 2010;7:288–98.

    Article  PubMed  Google Scholar 

  7. Iansante V, Mitry RR, Filippi C, Fitzpatrick E, Dhawan A. Human hepatocyte transplantation for liver disease: current status and future perspectives. Pediatr Res. 2018;83:232–40.

    Article  CAS  PubMed  Google Scholar 

  8. Der Lee K, Kuo TKC, Whang-Peng J, Chung YF, Lin CT, Chou SH, et al. In vitro hepatic differentiation of human mesenchymal stem cells. Hepatology. 2004;40:1275–84.

    Article  CAS  PubMed  Google Scholar 

  9. Hu C, Wu Z, Li L. Pre-treatments enhance the therapeutic effects of mesenchymal stem cells in liver diseases. J Cell Mol Med. 2020;24:40–9.

    Article  PubMed  Google Scholar 

  10. Miura M, Gronthos S, Zhao M, Lu B, Fisher LW, Robey PG, et al. SHED: stem cells from human exfoliated deciduous teeth. Proc Natl Acad Sci U S A. 2003;100:5807–12.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Yamaza T, Kentaro A, Chen C, Liu Y, Shi Y, Gronthos S, et al. Immunomodulatory properties of stem cells from human exfoliated deciduous teeth. Stem Cell Res Ther. 2010;1:5.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  12. Yamaza T, Alatas FS, Yuniartha R, Yamaza H, Fujiyoshi JK, Yanagi Y, et al. In vivo hepatogenic capacity and therapeutic potential of stem cells from human exfoliated deciduous teeth in liver fibrosis in mice. Stem Cell Res Ther. 2015;6:171.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  13. Sakai K, Yamamoto A, Matsubara K, Nakamura S, Naruse M, Yamagata M, et al. Human dental pulp-derived stem cells promote locomotor recovery after complete transection of the rat spinal cord by multiple neuro-regenerative mechanisms. J Clin Invest. 2012;122:80–90.

    CAS  PubMed  Google Scholar 

  14. Fujiyoshi J, Yamaza H, Sonoda S, Yuniartha R, Ihara K, Nonaka K, et al. Therapeutic potential of hepatocyte-like-cells converted from stem cells from human exfoliated deciduous teeth in fulminant Wilson’s disease. Sci Rep. 2019;9:1535.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  15. Takahashi Y, Yuniartha R, Yamaza T, Sonoda S, Yamaza H, Kirino K, et al. Therapeutic potential of spheroids of stem cells from human exfoliated deciduous teeth for chronic liver fibrosis and hemophilia a. Pediatr Surg Int. 2019;35:1379–88.

    Article  PubMed  Google Scholar 

  16. Desmet V, Roskams T, Van Eyken P. Ductular reaction in the liver. Pathol Res Pract. 1995;191:513–24.

    Article  CAS  PubMed  Google Scholar 

  17. Alvaro D, Mancino MG, Glaser S, Gaudio E, Marzioni M, Francis H, et al. Proliferating cholangiocytes: a neuroendocrine compartment in the diseased liver. Gastroenterology. 2007;132:415–31.

    Article  CAS  PubMed  Google Scholar 

  18. Clouston AD, Powell EE, Walsh MJ, Richardson MM, Demetris AJ, Jonsson JR. Fibrosis correlates with a ductular reaction in hepatitis C: roles of impaired replication, progenitor cells and steatosis. Hepatology. 2005;41:809–18.

    Article  CAS  PubMed  Google Scholar 

  19. Iwanaka T, Yamaza T, Sonoda S, Yoshimaru K, Matsuura T, Yamaza H, et al. A model study for the manufacture and validation of clinical-grade deciduous dental pulp stem cells for chronic liver fibrosis treatment. Stem Cell Res Ther. 2020;11:134.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  20. Van Cruchten STJ, De Waart DR, Kunne C, Hooiveld GJEJ, Boekschoten MV, Katan MB, et al. Absorption, distribution, and biliary excretion of cafestol, a potent cholesterol-elevating compound in unfiltered coffees, in mice. Drug Metab Dispos. 2010;38:635–40.

    Article  PubMed  CAS  Google Scholar 

  21. Dominici M, Le Blanc K, Mueller I, Slaper-Cortenbach I, Marini FCF, Krause DSDS, et al. Minimal criteria for defining multipotent mesenchymal stromal cells. The International Society for Cellular Therapy position statement. Cytotherapy. 2006;8:315–7.

    Article  CAS  PubMed  Google Scholar 

  22. Xiao SY, Wang HL, Hart J, Fleming D, Beard MR. Cdna arrays and immunohistochemistry identification of cd10/calla expression in hepatocellular carcinoma. Am J Pathol. 2001;159:1415–21.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  23. Nies AT, Keppler D. The apical conjugate efflux pump ABCC2 (MRP2). Pflugers Arch Eur J Physiol. 2007;453:643–59.

    Article  CAS  Google Scholar 

  24. Gissen P, Arias IM. Structural and functional hepatocyte polarity and liver disease. J Hepatol. 2015;63:1023–37.

    Article  PubMed  PubMed Central  Google Scholar 

  25. Lagana SM, Salomao M, Remotti HE, Knisely AS, Moreira RK. Bile salt export pump: a sensitive and specific immunohistochemical marker of hepatocellular carcinoma. Histopathology. 2015;66:598–602.

    Article  PubMed  Google Scholar 

  26. Turner R, Lozoya O, Wang Y, Cardinale V, Gaudio E, Alpini G, et al. Human hepatic stem cell and maturational liver lineage biology. Hepatology. 2011;53:1035–45.

    Article  CAS  PubMed  Google Scholar 

  27. Chaudhari P, Tian L, Deshmukh A, Jang YY. Expression kinetics of hepatic progenitor markers in cellular models of human liver development recapitulating hepatocyte and biliary cell fate commitment. Exp Biol Med. 2016;241:1653–62.

    Article  CAS  Google Scholar 

  28. Sacchetti B, Funari A, Michienzi S, Di Cesare S, Piersanti S, Saggio I, et al. Self-renewing osteoprogenitors in bone marrow sinusoids can organize a hematopoietic microenvironment. Cell. 2007;131:324–36.

    Article  CAS  PubMed  Google Scholar 

  29. Nishikawa Y, Sone M, Nagahama Y, Kumagai E, Doi Y, Omori Y, et al. Tumor necrosis factor-α promotes bile ductular transdifferentiation of mature rat hepatocytes in vitro. J Cell Biochem. 2013;114:831–43.

    Article  CAS  PubMed  Google Scholar 

  30. Shousha S, Gadir F, Peston D, Bansi D, Thillainaygam AV, Murray-Lyon IM. CD10 immunostaining of bile canaliculi in liver biopsies: change of staining pattern with the development of cirrhosis. Histopathology. 2004;45:335–42.

    Article  CAS  PubMed  Google Scholar 

  31. Zollner G. Hepatobiliary transporter expression in percutaneous liver biopsies of patients with cholestatic liver diseases. Hepatology. 2001;33:633–46.

    Article  CAS  PubMed  Google Scholar 

  32. Meier Y, Pauli-Magnus C, Zanger UM, Klein K, Schaeffeler E, Nussler AK, et al. Interindividual variability of canalicular ATP-binding-cassette (ABC)-transporter expression in human liver. Hepatology. 2006;44:62–74.

    Article  CAS  PubMed  Google Scholar 

  33. Stapelbroek JM, van Erpecum KJ, Klomp LWJ, Houwen RHJ. Liver disease associated with canalicular transport defects: current and future therapies. J Hepatol. 2010;52:258–71.

    Article  CAS  PubMed  Google Scholar 

  34. Li W, Li L, Hui L. Cell plasticity in liver regeneration. Trends Cell Biol. 2020;30:329–38.

    Article  PubMed  Google Scholar 

  35. Yovchev MI, Locker J, Oertel M. Biliary fibrosis drives liver repopulation and phenotype transition of transplanted hepatocytes. J Hepatol. 2016;64:1348–57.

    Article  PubMed  PubMed Central  Google Scholar 

  36. Tarlow BD, Pelz C, Naugler WE, Wakefield L, Wilson EM, Finegold MJ, et al. Bipotential adult liver progenitors are derived from chronically injured mature hepatocytes. Cell Stem Cell. 2014;15:605–18.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  37. Kalluri R, Weinberg RA. The basics of epithelial-mesenchymal transition. J Clin Invest. 2009;119:1420–8.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  38. Li CW, Xia W, Huo L, Lim SO, Wu Y, Hsu JL, et al. Epithelial-mesenchymal transition induced by TNF-α requires NF-κB-mediated transcriptional upregulation of Twist1. Cancer Res. 2012;72:1290–300.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  39. Unger C, Skottman H, Blomberg P. Sirac dilber M, Hovatta O. good manufacturing practice and clinical-grade human embryonic stem cell lines. Hum Mol Genet. 2008;17:R48–53.

    Article  CAS  PubMed  Google Scholar 

  40. Wang Y, Han ZB, Song YP, Han ZC. Safety of mesenchymal stem cells for clinical application. Stem Cells Int. 2012;652034.

  41. Gramignoli R, Tahan V, Dorko K, Venkataramanan R, Fox IJ, Ellis ECS, et al. Rapid and sensitive assessment of human hepatocyte functions. Cell Transplant. 2014;23:1545–56.

    Article  PubMed  Google Scholar 

  42. Stéphenne X, Najimi M, Dung KN, Smets F, Hue L, Guigas B, et al. Cryopreservation of human hepatocytes alters the mitochondrial respiratory chain complex 1. Cell Transplant. 2007;16:409–19.

    Article  PubMed  Google Scholar 

  43. Hirata M, Ishigami M, Matsushita Y, Ito T, Hattori H, Hibi H, et al. Multifaceted therapeutic benefits of factors derived from dental pulp stem cells for mouse liver fibrosis. Stem Cells Transl Med. 2016;5:1416–24.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  44. Sonoda S, Murata S, Nishida K, Kato H, Uehara N, Kyumoto-Nakamura Y, et al. Extracellular vesicles from deciduous pulp stem cells recover bone loss by regulating telomerase activity in an osteoporosis mouse model. Stem Cell Res Ther. 2020;11:296.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  45. Wang X, Willenbring H, Akkari Y, Torimaru Y, Foster M, Al-Dhalimy M, et al. Cell fusion is the principal source of bone-marrow-derived hepatocytes. Nature. 2003;422:897–901.

    Article  CAS  PubMed  Google Scholar 

  46. Quintana-Bustamante O, Alvarez-Barrientos A, Kofman AV, Fabregat I, Bueren JA, Theise ND, et al. Hematopoietic mobilization in mice increases the presence of bone marrow-derived hepatocytes via in vivo cell fusion. Hepatology. 2006;43:108–16.

    Article  PubMed  Google Scholar 

  47. Sato Y, Araki H, Kato J, Nakamura K, Kawano Y, Kobune M, et al. Human mesenchymal stem cells xenografted directly to rat liver are differentiated into human hepatocytes without fusion. Blood. 2005;106:756–63.

    Article  CAS  PubMed  Google Scholar 

  48. Ang LT, Tan AKY, Autio MI, Goh SH, Choo SH, Lee KL, et al. A roadmap for human liver differentiation from pluripotent stem cells. Cell Rep. 2018;22:2190–205.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgements

We would like to thank Editage (www.editage.com) for English language editing. We are very thankful to Ms. Tomoko Yamazaki (Department of Pediatric Surgery, Kyushu University) for her excellent assistance throughout this study. We are thankful to cell innovator (Fukuoka, Japan; www.editage.com) for their helpful microarray data analysis.

Funding

This work was supported by the Grants-in-Aid for Scientific Research (A) of the Japan Society for Promotion of Science (JSPS KAKENHI Grant Number 16H02682 and 25253094 to T.T.).

Author information

Authors and Affiliations

  1. Department of Pediatric Surgery, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan

    Ratih Yuniartha, Koichiro Yoshimaru, Toshiharu Matsuura & Tomoaki Taguchi

  2. Department of Anatomy, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada, Yogyakarta, Indonesia

    Ratih Yuniartha

  3. Department of Molecular Cell Biology and Oral Anatomy, Kyushu University Graduate School of Dental Science, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan

    Takayoshi Yamaza & Soichiro Sonoda

  4. Department of Pediatric Dentistry, Kyushu University Graduate School of Dental Science, Fukuoka, Japan

    Haruyoshi Yamaza

  5. Department of Anatomic Pathology, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan

    Yoshinao Oda

  6. Department of Pediatrics, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan

    Shouichi Ohga

  7. Fukuoka College of Health Sciences, Fukuoka, Japan

    Tomoaki Taguchi

Authors
  1. Ratih Yuniartha
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Takayoshi Yamaza
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Soichiro Sonoda
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Koichiro Yoshimaru
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Toshiharu Matsuura
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Haruyoshi Yamaza
    View author publications

    You can also search for this author in PubMed Google Scholar

  7. Yoshinao Oda
    View author publications

    You can also search for this author in PubMed Google Scholar

  8. Shouichi Ohga
    View author publications

    You can also search for this author in PubMed Google Scholar

  9. Tomoaki Taguchi
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

R.Y., generation, collection and assembly of data, interpretation of data, statistical analysis; T.Y., conception and design of the study, generation, collection and assembly of data, interpretation of data, statistical analysis, drafting of the manuscript; S.S., K.Y., T.M., H.Y., Y.O., S.O., generation, collection, and assembly of data; interpretation of data; T.T., conception and design, interpretation of data, critical revision of the manuscript, study supervision. All authors approved the final version of the manuscript.

Corresponding author

Correspondence to Takayoshi Yamaza.

Ethics declarations

Ethics approval and consent to participate

Human deciduous teeth were collected from discarded clinical samples from healthy pediatric donors (5–7 years) in the Department of Pediatric Dentistry, Kyushu University Hospital. Human sample handling was approved by Kyushu University Institutional Review Board for Human Genome/Gene Research (Protocol Number: 393–01). We obtained written informed consent from the parents of each patient on behalf of the child donors. All experimental procedures in this study were performed in accordance with the relevant guidelines and regulations.

Consent for publication

Not applicable.

Competing interests

The authors declare no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1.

Supplementary Methods. Supplementary References. Supplementary Table 1. The list of specific antibodies used for flow cytometry. Supplementary Table 2. Specific antibodies for immunohistochemistry and immunofluorescence. Supplementary Table 3. List of TaqMan probes for human genes. Supplementary Table 4. List of TaqMan probes for mouse genes. Supplementary Fig. 1. Characterization of stem cells from human exfoliated deciduous teeth (SHED). Supplementary Fig. 2. Hepatogenic properties of SHED. Supplementary Fig. 3. Expression of hepatic function-associated genes in SHED-Heps. Supplementary Fig. 4. Hepatic functions of SHED-Heps. Supplementary Fig. 5. Effects of SHED-Heps transplantation on liver fibrosis in CCl4-treated mice. Supplementary Fig. 6. Immunohistochemical control tests. Supplementary Fig. 7. Immunohistochemical specificity of antibodies against human leukocyte antigen A, B, and C (HLA-ABC), human hepatocyte paraffin 1 (HepPar1), human ALB, and human MME. Supplementary Fig. 8. Effects of SHED-Heps transplantation on MME expression in liver of CCl4-treated mice. Supplementary Fig. 9. Immunohistochemical localization of biliary transporter markers ATP-binding cassette subfamily B member 1 (ABCB1), ABCB11, and ABCC2. Supplementary Fig. 10. Distribution of biliary canaliculi markers in liver of SHED-Hep-transplanted CCl4-treated mice. Supplementary Fig. 11. Immunohistochemical localization of KRT19 and KRT7.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and Permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Yuniartha, R., Yamaza, T., Sonoda, S. et al. Cholangiogenic potential of human deciduous pulp stem cell-converted hepatocyte-like cells. Stem Cell Res Ther 12, 57 (2021). https://doi.org/10.1186/s13287-020-02113-8

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s13287-020-02113-8

Keywords

Stem Cell Research & Therapy

ISSN: 1757-6512