- Open Access
Rapid and high-efficiency generation of mature functional hepatocyte-like cells from adipose-derived stem cells by a three-step protocol
Stem Cell Research & Therapyvolume 6, Article number: 193 (2015)
The generation of functional hepatocytes is a major challenge for regenerative medicine and drug discovery. Here we show a method that facilitates generation of induced functional hepatocytes (iHeps) from adipose-derived stem cells (ADSCs) within 9 days. iHeps express hepatocytic gene programs and display functions characteristic of mature hepatocytes, including cytochrome P450 enzyme activity. Upon transplantation into mice with carbon tetrachloride (CCl4)-induced acute fulminant liver failure, iHeps restore the liver function and prolong survival. The work could contribute to the development of alternative strategies to obtain nonhepatic cell-derived mature hepatocytes with potential for biomedical and pharmaceutical applications.
Functional hepatocytes are in high demand in the field of regenerative medicine and drug development. They show great potential for repairing or replacing diseased and damaged tissues and can be valuable tools for pharmaceutical applications. However, the practical application of primary hepatocytes has been frustrated by their tendency to rapidly dedifferentiate and lose most hepatic functions after growth in a tissue culture environment [1–4]. To solve this dilemma, novel strategies for generating sufficient hepatocytes are in high demand. In the last few years, extrahepatic cell populations with potential to generate functional hepatocytes have been discovered [5–8]. Currently, attention is being given to mesenchymal stem cells (MSCs) [9, 10], which can be obtained from different sources such as bone marrow , amniotic fluid , umbilical cord blood , scalp tissue , placenta , or adipose tissue  of the body. These cells show the ability of multipotentiality and semi-infinite proliferation. In particular, adipose-derived stem cells (ADSCs) are recognized as one of the most promising MSCs identified thus far, since adipose tissue is ubiquitous and easily obtained in large quantities with little donor site morbidity or discomfort [17–20]. Furthermore, recent research has revealed that the use of ADSCs in regenerative medicine is not limited to mesodermal tissue but extended to both ectodermal and endodermal tissues and organs, although ADSCs originate from mesodermal lineages [21–25].
In the present study, we describe the generation of induced functional hepatocytes (iHeps) from rat ADSCs in a rapid and high-efficiency manner. iHeps express hepatocytic gene programs and possess the functional properties of mature hepatocytes, including albumin (ALB) secretion, urea synthesis, and cytochrome P (CYP) 450 enzyme activity. Notably, we demonstrate the therapeutic effects of iHeps on carbon tetrachloride (CCl4)-induced acute fulminant liver failure. These results indicate that iHeps could be applied in cellular therapies, disease modeling, and drug discovery.
Materials and methods
Isolation, culture, and identification of rat ADSCs
Isolation of ADSCs was performed as described previously  with some modifications. The inguinal fat pad was collected under sterile conditions from 5-week-old female Lewis rats (Vital River Laboratory, Chengdu, Sichuan, P.R. China) and washed with Hank’s balanced salt solution (HBSS; Gibco, Chengdu, Sichuan, P.R. China). The washing step was usually repeated three times. Adipose tissue sample was minced into small pieces and digested in 0.1 % collagenase type I (3 ml for each 1 g tissue; Gibco) at 37 °C for 1 hour with a rotation speed of 120 rpm. After digestion, an equal volume of low-glucose Dulbecco’s modified Eagle’s medium (DMEM-LG; Gibco) containing 10 % fetal bovine serum (FBS; Gibco) was added. The cell suspension was filtered through a 100 μm filter (BD Falcon, Chengdu, Sichuan, P.R. China) for the removal of the solid aggregates. The sample was subsequently centrifuged at 1500 rpm for 10 minutes at 4 °C and completed the separation of the stromal cells from the adipocytes. The centrifugation step was repeated. The cells were resuspended in complete medium (DMEM-LG with 10 % FBS, 100 U/ml penicillin, and 100 μg/ml streptomycin) in a 75 cm2 culture dish and were maintained at 37 °C in saturated humidity with 5 % carbon dioxide. After 1 day, nonadherent cells were removed by two or three washes with HBBS and medium changes were performed every 2 days thereafter. Cell morphology was monitored under an inverted microscope. Passage 3 cells were used for flow cytometry analysis and differentiation assays.
For flow cytometry analysis, 5 × 105 ADSCs (in 100 μl phosphate-buffered saline (PBS)) were incubated with different fluorescently labeled monoclonal antibodies (anti-rat CD45-PECy5, anti-rat CD31-PE, anti-rat CD29-FITC, anti-rat CD44H-FITC, and anti-rat CD90-FITC; Biolegend, Chengdu, Sichuan, P.R. China) and incubated in the dark at 2–8 °C for 30 minutes. After washing twice with PBS, cells were resuspended in 300 μl PBS and analyzed by the Calibur flow cytometer (BD Biosciences, Chengdu, Sichuan, P.R. China).
For adipocytic differentiation, ADSCs (5 × 103 cells/cm2) were seeded in six-well plates. When ~100 % confluent, cells were maintained in adipocyte genesis medium (PT-3004; Lonza, Chengdu, Sichuan, P.R. China) for 2 weeks. Cells were then stained with Oil red O.
For osteogenic differentiation, ADSCs (5 × 103 cells/cm2) were seeded in six-well plates. When ~100 % confluent, cells were treated with inducing medium (PT-3002; Lonza) for 3 weeks. Cells were then fixed with 4 % formaldehyde for 30 minutes and stained with Alizarin Red.
For chondrogenic differentiation, ADSCs were seeded at a density of 106 per well in an ultralow attachment six-well plate, and cultured with inducing medium (PT-3003; Lonza) for 3 weeks. Cells were then identified by Alcian blue staining.
In vitro differentiation of ADSCs into iHeps
At passages 3–7, the cells were seeded on collagen type I-coated culture dishes at a concentration of 2.0 × 104 cells/cm2. When the cells reached 100 % confluence, hepatic induction was carried out over a period of 9 days (Table 1). First, the cells were treated for 1 day of endodermal induction with RPMI-1640 (Gibco) supplemented with 100 nM IDE1 (Tocris, Chengdu, Sichuan, P.R. China) and 3 μΜ CHIR99021 (Selleckchem, Chengdu, Sichuan, P.R. China). During the next step, the culture medium was replaced with hepatogenic induction medium containing 100 nM IDE1, 20 ng/ml fibroblast growth factor 4 (FGF4; PeproTech, Chengdu, Sichuan, P.R. China), and 150 ng/ml hepatocyte growth factor (HGF; PeproTech). Finally, during the maturation step, the cells were cultured in Williams’ E (Gibco) supplemented with 50 ng/ml HGF, 20 ng/ml epidermal growth factor (EGF; PeproTech), 30 ng/ml oncostatin M (OsM; PeproTech), 2 × 10−5 mol/l dexamethasone (Dex; Sigma, Chengdu, Sichuan, P.R. China) and 1 × insulin–transferrin–selenium (ITS; Sigma).
Flow cytometry analysis
For intracellular staining of ALB and alpha-1-antitrypsin (AAT), 5 × 105 iHeps were harvested and fixed with 4 % paraformaldehyde for 30 minutes, and then permeabilized in staining buffer (BD Biosciences) for 10 minutes. Cells were then incubated with primary antibody—sheep anti-ALB (Bethyl, Chengdu, Sichuan, P.R. China) and rabbit anti-AAT (American Research Products, Chengdu, Sichuan, P.R. China)—for 30 minutes in staining buffer, followed by secondary antibody—dylight 488 conjugated donkey anti-rabbit IgG (Bethyl) and dylight 594 conjugated donkey anti-sheep IgG (Bethyl)—incubation for 30 minutes. Cells were analyzed by the Calibur flow cytometer (BD Biosciences).
For detecting of asialoglycoprotein receptor (ASGPR), 5 × 105 iHeps (in 100 μl PBS) were incubated with monoclonal antibodies (anti-ASGPR1-PE; Santa Cruz, Chengdu, Sichuan, P.R. China) and incubated in the dark at 2–8 °C for 30 minutes. After washing twice with PBS, cells were resuspended in 300 μl PBS and analyzed by the Calibur flow cytometer (BD Biosciences).
For intracellular staining of ALB and AAT, the cells were fixed with 4 % paraformaldehyde for 15 minutes at room temperature and then incubated with PBS containing 0.2 % Triton X-100 (Sigma) for 15 minutes. Cells were then washed three times with PBS. After being blocked by 3 % bovine serum albumin (BSA) in PBS for 60 minutes at room temperature, cells were incubated with primary antibodies at 4 °C overnight, washed three times with PBS, and then incubated with appropriate fluorescence-conjugated secondary antibody for 60 minutes at 37 °C in the dark. Nuclei were stained with 4',6-diamidino-2-phenylindole (DAPI; Sigma). Primary and secondary antibodies were diluted in PBS containing 3 % BSA. Antibodies used for immunofluorescence are as follows: sheep anti-ALB (1:500; Bethyl), rabbit anti-AAT (1:1; Abcam, Chengdu, Sichuan, P.R. China), rabbit anti-hepatocyte nuclear factor alpha-4 (anti-HNF4α, 1:50; Santa Cruz), rabbit anti-Ki67 (1:100; Santa Cruz), dylight 488 conjugated donkey anti-rabbit IgG (1:200; Bethyl), dylight 594 conjugated donkey anti-sheep IgG (1:200; Bethyl), and Alexa Fluor 594 conjugated goat anti-rabbit IgG (1:100; ZSBG-BIO, Chengdu, Sichuan, P.R. China).
Real-time quantitative PCR
Total RNA was isolated from ADSCs, iHeps, and primary rat hepatocytes (rHeps) using the Trizol Reagent (Sigma). Additional file 1 shows the sequences of both forward and reverse primers in more detail. In parallel, we analyzed the mRNA concentration of the rat housekeeping GAPDH as an internal control for normalization. The real-time monitoring of the PCR reaction, the precise quantification of the products in the exponential phase of the amplification, and the melting curve analysis were performed with the Bio-Rad CFX Manager software (Chengdu, Sichuan, P.R. China), as recommended by the manufacturer.
Gene expression profile analysis
Total RNA was extracted and reverse transcript into cDNA. Samples were then hybridized to the Affymetrix Rat Gene 1.0ST (Chengdu, Sichuan, P.R. China) in accordance with the manufacturer’s instruction. Data were normalized by Partek Genomics Suite 6.6 (Affymetrix, Beijing, P.R. China) in default analysis settings. Normalized data were processed to the Kyoto Encyclopedia of Genes and Genomes (KEGG, Chengdu, Sichuan, China) for further pathway function analysis.
Periodic acid–Schiff staining, acetylated low-density lipoprotein, and indocyanine green uptake assays, ALB ELISA, and urea synthesis
iHeps were stained by Periodic acid–Schiff (PAS; Sigma) following the manufacturer’s instructions. For the acetylated low-density lipoprotein (ac-LDL) uptake assay, iHeps were incubated with 10 mg/ml DiI-labeled ac-LDL (Life Technologies, Chengdu, Sichuan, China) at 37 °C for 1 hour and later washed three times with PBS. For the indocyanine green (ICG; Sigma) uptake assay, media of iHeps were changed with 1 mg/ml ICG and incubated at 37 °C for 1 hour, followed by washing three times with PBS. To determine ALB secretion in iHeps, culture supernatants were collected daily and determined by the rat ALB ELISA kit (Bethyl) according to the manufacturer’s instructions. Urea content was measured with diacetylmonoxime with a commercially available kit (StanBio Laboratory, Chengdu, Sichuan, China).
iHep transplantation to CCl4-induced acute fulminant liver failure mice
NPG mice (6 weeks old, male; Beijing Vitalstar Biotechnology Co., Ltd, Chengdu, Sichuan, China) were injected with CCl4 (Sigma) at a dose of 0.5 ml/kg body weight through intraperitoneal injection. Eight hours after CCl4 treatment, ADSCs, iHeps, and rHeps (2 × 106 cells/animal) were injected into the spleens of the mice. Meanwhile, a sham operation group was used as negative control. Blood and liver samples were collected after the surviving animals were sacrificed. Blood samples were used for blood biochemical analysis. Livers of recipient mice were embedded in Tissue Freezing Medium (Leica, Chengdu, Sichuan, China) and then frozen in liquid nitrogen. Cryostat sections (8 μm) were stained. All animal experiments were in conformity with NIH guidelines (NIH Pub. No. 85-23, revised 1996) and were approved by the Animal Care and Use Committee of Sichuan University, Chengdu, P.R. China.
In vivo tumor transplantation assay
Five BALB/c nude mice (6 weeks old, female; HFK Bioscience, Beijing, China) were subcutaneously injected with HepG2 or iHeps (1 × 106) on both sides of the back. These mice were sacrificed 8 weeks after transplantation. All animal experiments were in conformity with NIH guidelines (NIH Pub. No. 85-23, revised 1996) and were approved by the Animal Care and Use Committee of Sichuan University.
Results and discussion
Characterization of ADSCs
The cultures were observed using an inverted light microscope. Attachment of spindle-shaped cells to the culture dish was observed after 1 day of culture (Fig. 1a). Primary cultures reached 80–90 % confluence in approximately 4–5 days. During passaging, the cell growth tended to accelerate and the morphology of cells changed gradually. After three passages, the cultures showed homogeneous fibroblastic morphology (Fig. 1b). Flow cytometry analysis showed that ADSCs possessed the surface marker profiles (CD29, CD44, and CD90) typical for MSCs, and were negative for hematopoietic marker (CD45) or endothelial marker (CD31) indicating the absence of hematopoietic and endothelial cells (Fig. 1c). When cultured in appropriate induction medium, ADSCs differentiated into adipocytes, which were verified by Oil red O staining (Fig. 1d). They were also able to differentiate into osteocytes, which were confirmed by Alizarin Red staining (Fig. 1d). Furthermore, they could differentiate into chondrocytes, which were identified by Alcian blue binding assay (Fig. 1d).
Screening for induction protocols to generate iHeps from ADSCs
For rapidly and highly efficiently generating mature hepatocytes from ADSCs, we screened a series of hepatogenic induction strategies and finally confirmed a three-step protocol which was described in Materials and methods. In this protocol, ADSCs were allowed to reach approximately 100 % confluence on collagen type I-coated dishes, and were then treated with endodermal induction medium on day 0 (Fig. 2a, I) in the presence of IDE1 and CHIR99021. After 1 day, the cell morphology turned from a long spindle shape into a short spindle shape (Fig. 2a, II). Immunofluorescent staining revealed that most of the cells were positive for the definitive endoderm (DE) markers Sox17 and FoxA2 (Fig. 2b), indicating that the ADSCs efficiently differentiated into DE during the endodermal induction step. Following the endodermal induction step, cells were treated with the hepatogenic induction medium for 3 days, which changed the cell morphology from a spindle shape to a polygonal shape (Fig. 2a, III). Finally, the medium was replaced with maturation medium which resulted in the cell morphology changing into a typical cuboidal shape of primary hepatocytes that had tight cell–cell contact (Fig. 2a, IV). Flow cytometry analysis of these hepatocyte-like cells (that is, iHeps) confirmed that nearly 100 % of iHeps were ALB-positive, ~95 % were AAT-positive, and ~91 % were ASGPR1-positive, indicating that iHeps possess these typical markers of mature hepatocytes (Fig. 2c). Furthermore, the expression of genes specific for mature hepatocytes (for example, ALB, ASGPR1, and Transferrin) increased gradually during iHep induction, while the expression of alpha fetal protein (AFP) for immature hepatocytes significantly upgraded in the hepatogenic induction stage and descended to the level of rHeps in the maturation step, suggesting that hepatic lineage differentiation is a progressively coordinated process (Fig. 2d). These results indicate that we successfully obtain ADSC-derived mature hepatocytes using a new procedure.
iHeps possess the typical characteristics of mature hepatocytes
Immunofluorescent staining showed that more than 90 % of iHeps expressed both ALB and AAT at day 9 (Fig. 3a), suggesting a highly-efficient hepatogenic differentiation. To assess the metabolic activity of iHeps, we quantified ALB production and urea synthesis. We found that iHeps had a remarkable capability for secreting the plasma protein ALB at a level close to rHeps at day 9 (Fig. 3b). The cumulative urea amounts also gradually increased in the iHep culture system during the induction period (Fig. 3c). Genome-wide expression profile analysis revealed that iHeps were clustered closely with cultured rHeps (Fig. 3d). Furthermore, gene set enrichment analysis showed that pathways enriched in rHeps were significantly enriched in iHeps, including those involved in glucose metabolism, lipid metabolism, amino acid metabolism, and phase I and phase II detoxification (see Additional file 2). These data indicate that ADSCs undergo hepatic differentiation by transcriptional alterations. In accordance with the expression of hepatic genes, iHeps displayed numerous hallmark functions of mature hepatocytes, such as glycogen storage, ac-LDL intake, and ICG uptake (Fig. 3e). The drug metabolic capacity is one of the most important functions that distinguish hepatocytes. CYP450 enzymes of hepatocytes are the main enzymes accounting for drug metabolism. Their activities and responses to specific inducers are used to evaluate drug metabolism of hepatocytes. We quantitatively confirmed the expression of CYP enzymes in iHeps, CYP1A1, CYP1A2, CYP2A1, CYP2C7, CYP2C12, CYP2E1, and CYP3A1. Results showed that iHeps already expressed these genes at remarkable levels without addition of chemical inducers (Fig. 3f). Furthermore, chemical inducers (3-methylcholanthrene, phenobarbital, and acetone) could markedly induce mRNA expression levels of CYP1A1, CYP1A2, CYP2A1, CYP2E1, and CYP3A1, except for CYP2C7 and CYP2C12 (Fig. 3g). Importantly, in another assay for CYP activities, iHeps displayed CYP enzyme-dependent metabolism of phenacetin, coumarin, and chlorzoxazone (Fig. 3h). These results offer the possibility of using iHeps for toxicity screening during drug discovery.
iHeps improve CCl4-induced acute fulminant liver failure
To evaluate whether iHeps have sufficient hepatic functions to support the liver in recovering from acute fulminant hepatitis, NPG mice (T, B, and natural killer cell-depleted mice) were injected with CCl4 to trigger acute fulminate hepatitis and animal death within 24 hours (Fig. 4a). ADSCs, iHeps, and rHeps were separately injected intrasplenically into NPG mice 8 hours after CCl4 treatment (Fig. 4a). In groups of mice transplanted with ADSCs or sham operation, almost all recipients died within 24 hours after CCl4 treatment (one mouse in the sham operation group died at day 2; Fig. 4b). rHep transplant significantly improved the survival rate and extended the survival time of mice with acute liver failure (Fig. 4b). Remarkably, upon transplant with iHeps, two of five mice completely recovered from CCl4-induced acute fulminant liver failure (Fig. 4b) and showed normal serum alanine transaminase (ALT) and glutamic-oxaloacetic transaminase (AST) levels on day 7 after CCl4 treatment (Fig. 4c, d). Rat ALB was also detected in the sera of mice transplanted with iHep cells (Fig. 4e). Histological analysis revealed that iHeps significantly improved recovery from CCl4-induced liver damage (Fig. 4f, g). Immunofluorescence staining of rat ALB showed the repopulation of iHeps in the liver parenchyma in the surviving mice, and repopulated ALB-positive cells were positively stained by AAT, an antibody labeling both rat and mouse hepatocytes (Fig. 4h). Remarkably, iHeps did not fuse with mouse hepatocytes as determined by immunofluorescent staining using antibodies specifically against rat ALB and mouse HNF4α (see Additional file 3). These results indicate that iHeps can populate the liver and have a therapeutic effect in the treatment of acute fulminant liver failure. Intriguingly, repopulated iHeps were not proliferating as shown by Ki67 staining 8 weeks after transplantation (see Additional file 3). Furthermore, we found that iHeps did not form tumors after transplantation in immunodeficient mice (see Additional file 4). Together, our data indicate that iHeps possess notable mature hepatocyte functions to support the liver in recovering from acute fulminant failure.
Several studies have described the differentiation of ADSCs into cells that display hepatocytic characteristics [27–30]. However, those in vitro differentiation methods are not applicable to practical use because about 1 month is required to induce ADSCs into cells with hepatic functions. Applications in the current study require a special approach, such as shortening as much as possible, including cultivation and direct hepatic fate. In this work, we presented a protocol which allowed ADSCs to differentiate into functional hepatocytes in a short time. Nine days is sufficient to obtain cells, which shows hepatocyte-specific morphology, expression profiles, and functions. To our knowledge, this is the first time such a short hepatogenic differentiation protocol has been presented. In this protocol, ADSCs are first exposed to a high level of transforming growth factor beta (TGF-β)/activin/nodal (IDE1) and Wnt (CHIR99021) signaling in a manner that is designed to mimic events during embryonic development in order to allow DE formation . IDE1 is a small molecule compound and could induce DE differentiation up to 80 % of mouse embryonic stem cells (mESCs) (or 50 % of human embryonic stem cells (hESCs)) in the absence of activin A (a typically used DE inducer) [32, 33]. Similar to activin A, IDE1 induces Smad2 phosphorylation in mESCs, while their targets remain unknown. In our study, a combination of IDE1 and CHIR99021 (a specific chemical inhibitor of GSK3) was able to efficiently drive ADSCs in a definitive commitment to endoderm formation. Compared with cells cultured in media without CHIR99021 (data not shown), we found that the presence of CHIR99021 might have a synergistic effect with IDE1 and was able to efficiently induce a rapid increase in the expression of the DE markers Sox17 and FoxA2. The cell morphology of ADSCs also quickly changes into a short spindle shape within 1 day. This enables ADSCs to differentiate into hepatocytes quickly and efficiently. Unlike the recent studies [34–36], our data showed that more than 90 % of iHeps efficiently expressed both ALB and AAT and secreted the plasma protein ALB at a level close to primary rHeps after 9 days of induction. Furthermore, iHeps possessed remarkable CYP enzyme activity which was associated with drug metabolism. Additionally, transplanted iHeps could repopulate livers of NPG mice with acute fulminant liver failure and restore the liver function. Taken together, our study provides a simple, rapid, and high-efficiency protocol for the generation of ADSC-derived iHeps suitable for cell-based therapy, as well as an in vitro drug screening model.
In summary, our study outlines rapid generation of mature functional hepatocyte cells from ADSCs by an efficient three-step induction protocol. Furthermore, we have shown therapeutic effects of these cells on CCl4-induced acute fulminant liver failure. This work could contribute to the development of alternative strategies to obtain nonhepatic cell-derived mature hepatocytes with potential for biomedical and pharmaceutical applications.
Acetylated low-density lipoprotein
Adipose-derived stem cell
Bovine serum albumin
- CCl4 :
Low-glucose Dulbecco’s modified Eagle’s medium
Epidermal growth factor
Enzyme-linked immunosorbent assay
Fetal bovine serum
Fibroblast growth factor 4
Hank’s balanced salt solution
Hepatocyte growth factor
Hepatocyte nuclear factor alpha-4
Induced functional hepatocyte
Kyoto Encyclopedia of Genes and Genomes
Mesenchymal stem cell
Primary rat hepatocyte
Transforming growth factor beta
Shulman M, Nahmias Y. Long-term culture and coculture of primary rat and human hepatocytes. Methods Mol Biol. 2013;945:287–302.
Pichard L, Raulet E, Fabre G, Ferrini JB, Ourlin JC, Maurel P. Human hepatocyte culture. Methods Mol Biol. 2006;320:283–93.
Cascio SM. Novel strategies for immortalization of human hepatocytes. Artif Organs. 2001;25:529–38.
Runge D, Michalopoulos GK, Strom SC, Runge DM. Recent advances in human hepatocyte culture systems. Biochem Biophys Res Commun. 2000;274:1–3.
Takayama K, Inamura M, Kawabata K, Katayama K, Higuchi M, Tashiro K, et al. Efficient generation of functional hepatocytes from human embryonic stem cells and induced pluripotent stem cells by HNF4α transduction. Mol Ther. 2012;20:127–37.
Huang P, Zhang L, Gao Y, He Z, Yao D, Wu Z, et al. Direct reprogramming of human fibroblasts to functional and expandable hepatocytes. Cell Stem Cell. 2014;14:370–84.
Schwartz RE, Fleming HE, Khetani SR, Bhatia SN. Pluripotent stem cell-derived hepatocyte-like cells. Biotechnol Adv. 2014;32:504–13.
Subramanian K, Owens DJ, Raju R, Firpo M, O'Brien TD, Verfaillie CM, et al. Spheroid culture for enhanced differentiation of human embryonic stem cells to hepatocyte-like cells. Stem Cells Dev. 2014;23:124–31.
Volarevic V, Nurkovic J, Arsenijevic N, Stojkovic M. Concise review: therapeutic potential of mesenchymal stem cells for the treatment of acute liver failure and cirrhosis. Stem Cells. 2014;32:2818–23.
Liu WH, Song FQ, Ren LN, Guo WQ, Wang T, Feng YX, et al. The multiple functional roles of mesenchymal stem cells in participating in treating liver diseases. J Cell Mol Med. 2015;19:511–20.
Pittenger MF, Mackay AM, Beck SC, Jaiswal RK, Douglas R, Mosca JD, et al. Multilineage potential of adult human mesenchymal stem cells. Science. 1999;284:143–7.
De Coppi P, Bartsch Jr G, Siddiqui MM, Xu T, Santos CC, Perin L, et al. Isolation of amniotic stem cell lines with potential for therapy. Nat Biotechnol. 2006;25:100–6.
Bieback K, Kern S, Kluter H, Eichler H. Critical parameters for the isolation of mesenchymal stem cells from umbilical cord blood. Stem Cells. 2004;22:625–34.
Shih DT, Lee DC, Chen SC, Tsai RY, Huang CT, Tsai CC, et al. Isolation and characterization of neurogenic mesenchymal stem cells in human scalp tissue. Stem Cells. 2005;7:1012–20.
In 't Anker PS, Scherjon SA, Kleijburg-van der Keur C, de Groot-Swings GM, Claas FH, Fibbe WE, et al. Isolation of mesenchymal stem cells of fetal or maternal origin from human placenta. Stem Cells. 2004;22:1338–45.
Zuk PA, Zhu M, Mizuno H, Huang J, Futrell JW, Katz AJ, et al. Multilineage cells from human adipose tissue: implications for cell-based therapies. Tissue Eng. 2001;7:211–28.
Gimble JM, Katz AJ, Bunnell BA. Adipose-derived stem cells for regenerative medicine. Circ Res. 2007;100:1249–60.
Gimble JM, Guilak F, Bunnell BA. Clinical and preclinical translation of cell-based therapies using adipose tissue-derived cells. Stem Cell Res Ther. 2010;1:19.
Gimble JM, Bunnell BA, Guilak F. Human adipose-derived cells: an update on the transition to clinical translation. Regen Med. 2012;7:225–35.
Kokai LE, Marra K, Rubin JP. Adipose stem cells: biology and clinical applications for tissue repair and regeneration. Transl Res. 2014;163:399–408.
Feng N, Han Q, Li J, Wang S, Wang S, Li H, Yao X, et al. Generation of highly purified neural stem cells from human adipose-derived mesenchymal stem cells by Sox1 activation. Stem Cells Dev. 2014;23:515–29.
Yang Q, Du X, Fang Z, Xiong W, Li G, Liao H, et al. Effect of calcitonin gene-related peptide on the neurogenesis of rat adipose-derived stem cells in vitro. PLoS One. 2014;9:e86334.
Karaoz E, Okcu A, ünal ZS, Subasi C, Saglam O, Duruksu G. Adipose tissue-derived mesenchymal stromal cells efficiently differentiate into insulin-producing cells in pancreatic islet microenvironment both in vitro and in vivo. Cytotherapy. 2013;15:557–70.
Li J, Zhu L, Qu X, Lin R, Liao L, Wang J, et al. Stepwise differentiation of human adipose-derived mesenchymal stem cells toward definitive endoderm and pancreatic progenitor cells by mimicking pancreatic development in vivo. Stem Cells Dev. 2013;22:1576–87.
Khorsandi L, Khodadadi A, Nejad-Dehbashi F, Saremy S. Three-dimensional differentiation of adipose-derived mesenchymal stem cells into insulin-producing cells. Cell Tissue Res. 2015;361(3):745–53. doi:10.1007/s00441-015-2140-9. Epub 2015 Mar 21.
Bunnell BA, Flaat M, Gagliardi C, Patel B, Ripoll C. Adipose-derived stem cells: isolation, expansion and differentiation. Methods. 2008;45:115–20.
Aurich H, Sgodda M, Kaltwasser P, Vetter M, Weise A, Liehr T, et al. Hepatocyte differentiation of mesenchymal stem cells from human adipose tissue in vitro promotes hepatic integration in vivo. Gut. 2009;58:570–81.
Okura H, Komoda H, Saga A, Kakuta-Yamamoto A, Hamada Y, Fumimoto Y, et al. Properties of hepatocyte-like cell clusters from human adipose tissue-derived mesenchymal stem cells. Tissue Eng Part C. 2010;16:761–70.
Xu D, Nishimura T, Zheng M, Wu M, Su H, Sato N, et al. Enabling autologous human liver regeneration with differentiated adipocyte stem cells. Cell Transplant. 2014;23:1573–84.
Li X, Yuan J, Li W, Liu S, Hua M, Lu X, et al. Direct differentiation of homogeneous human adipose stem cells into functional hepatocytes by mimicking liver embryogenesis. Cell Physiol. 2014;229:801–12.
JHay DC, Fletcher J, Payne C, Terrace JD, Gallagher RC, Snoeys J, et al. Highly efficient differentiation of hESCs to functional hepatic endoderm requires ActivinA and Wnt3a signaling. Proc Natl Acad Sci U S A. 2008;105:12301–6.
Borowiak M, Maehr R, Chen S, Chen AE, Tang W, Fox JL, et al. Small molecules efficiently direct endodermal differentiation of mouse and human embryonic stem cells. Cell Stem Cell. 2009;4:348–58.
Li W, Jiang K, Ding S. Concise review: a chemical approach to control cell fate and function. Stem Cells. 2012;30:61–8.
Yin L, Zhu Y, Yang J, Ni Y, Zhou Z, Chen Y, et al. Adipose tissue-derived mesenchymal stem cells differentiated into hepatocyte-like cells in vivo and in vitro [J]. Mol Biol Rep. 2015;11:1722–32.
Sarvandi SS, Joghataei MT, Parivar K, Khosravi M, Sarveazad A, Sanadgol N. In vitro differentiation of rat mesenchymal stem cells to hepatocyte lineage. Iranian J Basic Med Sci. 2015;18:89–97.
Han SM, Coh YR, Ahn JO, Jang G, Yum SY, Kang SK, et al. Enhanced hepatogenic transdifferentiation of human adipose tissue mesenchymal stem cells by gene engineering with Oct4 and Sox2. PLoS One. 2015;10:e0108874.
This work was supported by the Hi-tech Research and Development Program (863 Program) of China (2012AA021004), Key Programs for Science and Technology Development of Sichuan Province (2014SZ0122), and New Century Excellent Talents in University of China (NCET-11-0342).
The authors declare that they have no competing interests.
FX, JL, JD, and HD were involved in drafting the manuscript and critically revising it for important intellectual content. FX, JL, and JD equally shared the majority of writing and editing. FX, JL, JD, XC, YW, PX, LC, YF, FC, YY, and YZ performed the experiments and acquired the data. FX, JL, JD, MH, DY, YqW, and HD were involved in data analysis and interpretation. HD gave final approval of the version to be published. All authors read and approved the manuscript.
Fen Xu, Junli Liu and Jie Deng contributed equally to this work.
Showing hepatic pathways enriched in rHeps and iHeps cells, related to Fig. 3. (PDF 98 kb)
Showing transplantation of iHeps into NPG mice, related to Fig. 4. A Cell fusion between repopulated iHeps and recipient mouse hepatocytes were excluded by co-staining of rat AlB (green) and mouse HNF4α (red). Antibody specific for rat ALB stained iHeps, while antibody specific for mouse HNF4α stained mouse hepatocytes. B Sections of NPG livers 8 weeks after iHep transplantation were stained by rat ALB (green), rat and mouse Ki67 (red) antibodies. iHeps were positively stained for rat ALB, but were negatively stained for rat and mouse Ki67. Scale bars: 50 μm A, B. (PDF 193 kb)