A subset of mobilized human hematopoietic stem cells express germ layer lineage genes which can be modulated by culture conditions
- Tapas Makar1, 2, 3,
- Vamshi K. Nimmagadda1, 3,
- Poornachander R. Guda1, 3,
- Brian Hampton4,
- Weiliang Huang5, 6,
- Maureen A. Kane5, 6,
- Paul S. Fishman1, 3,
- Bernard Pessac^7, 8,
- Christopher T. BeverJr.1, 2, 3Email authorView ORCID ID profile and
- David Trisler1, 2, 3
© The Author(s). 2018
Received: 12 December 2017
Accepted: 2 April 2018
Published: 2 May 2018
Adult bone marrow contains stem cells that replenish the myeloid and lymphoid lineages. A subset of human and mouse CD34+ bone marrow stem cells can be propagated in culture to autonomously express embryonic stem cell genes and embryonic germ layer lineage genes. The current study was undertaken to determine whether these CD34+ stem cells could be obtained from human blood, whether gene expression could be modulated by culture conditions and whether the cells produce insulin.
Human peripheral blood buffy coat cells and mobilized CD34+ cells from human blood and from blood from C57Bl/6 J mice were cultured in hybridoma medium or neural stem cell induction medium supplemented with interleukin (IL)-3, IL-6, and stem cell factor (SCF). Changes in mRNA and protein expression were assessed by Western blot analysis and by immunohistochemistry. Mass spectrometry was used to assess insulin production.
We were able to culture CD34+ cells expressing embryonic stem cell and embryonic germ layer lineage genes from adult human peripheral blood after standard mobilization procedures and from mouse peripheral blood. Gene expression could be modulated by culture conditions, and the cells produced insulin in culture.
These results suggest a practical method for obtaining large numbers of CD34+ cells from humans to allow studies on their potential to differentiate into other cell types.
Adult bone marrow contains stem cells that replenish the myeloid and lymphoid lineages throughout life [1, 2]. In addition to the expected hematopoietic stem cell genes CD34, cKit, and CD45 , a subset of these adult human and mouse CD34+ bone marrow stem cells express the embryonic stem cell genes Oct-4, Sox-2, LIN-28 , and embryonic germ layer lineage genes such as ectodermal neuronal (neurofilament, tubulin) and oligodendroglial (NG-2, MOG, PLP, MBP (human)), mesodermal cardiac (MEF, troponin C, MLC-2), and endodermal pancreatic (Pdx-1, Ptf1α, Ngn-3, FoxA2, Sox17, CXCR4, Hnf1B, Hnf4A, Hnf6, Nkx2.2, Pax-6, GLUT2, glucokinase, proinsulin and insulin (human)) and intestinal (villin) genes . A cell culture method was developed to propagate a pure population of this subset of CD34+ stem cells . The gene expression profile suggested that this subset of CD34+ stem cells might have characteristics of embryonic stem cells and might be capable of developing into cell types other than myeloid and lymphoid cells. To test this possibility, adult mouse CD34+ bone marrow stem cells were expanded in culture, labeled, and inserted into mouse blastocysts to determine their fates in the mice that developed. It was found that the labeled cells formed multiple organs in chimeric mice suggesting that, when placed in the proper conditions, the cells could differentiate into multiple different lineages . While our early animal studies [6, 8] and those of others and a series of case reports suggested that adult CD34+ stem cells could transdifferentiate to nonhematogenous cell types when transplanted into adults, this remains controversial because of findings of fusion of CD34+ stem cells with tissue-specific cells (reviewed in Porada et al. ) and findings suggesting that CD34 is a common marker of diverse progenitors (reviewed in Sidney et al. ). The current study was undertaken to determine whether CD34+ stem cells that could be induced to express embryonic germ layer lineage genes could be obtained from mobilized human peripheral blood, whether the cells so generated expressed proteins not expected in hematogenous stem cells in conditions where cell fusion was not possible, and whether gene expression could be modulated by culture conditions.
Human buffy coat cells and CD34+ cells from peripheral blood were purchased from ALLCELLS (Alameda, CA, USA). Human buffy coat cells were obtained by differential centrifugation of blood from normal donors. The human CD34+ cells had been mobilized by the company by injecting donors with five daily injections of granulocyte macrophage colony-stimulating factor (GCSF). Blood was then collected and CD34+ cells were obtained by flow cytometry. We received 1 × 106 CD34+ hematopoietic stem cells pooled from multiple donors that were put directly into culture as described below.
Human bone marrow cells were purchased from a commercial vendor (Lonza, Inc., Walkersville, MD, USA) and separated by differential centrifugation as described previously . CD34+ cells were grown as described below.
Blood was obtained from C57Bl/6 J mice by cardiac puncture, buffy coats obtained by differential centrifugation, and CD34+ stem cells grown as described below. All procedures were performed in accordance with the approved University of Maryland School of Medicine Institutional Animal Care and Use Committee Protocol. National Institutes of Health guidelines for animal treatment and care were followed assiduously.
Human CD34+ stem cells were cultured from bone marrow-derived buffy coat or in situ mobilized CD34+ bone marrow stem cells by culture in GIBCO Hybridoma serum-free medium and GIBCO protein-free medium each supplemented with 10 ng/ml human interleukin (IL)-3, 5 ng/ml human IL-6, 10 ng/ml human stem cell factor (SCF), and β-mercaptoethanol in T75 tissue culture flasks as reported previously . Only suspended cells were retained at each passage; cells adherent to the flask were discarded. At each passage 2 × 106 suspension cells were replated in a new T75 flask. No feeder cells or matrix were employed.
To investigate whether culture conditions could be used to modulate gene expression in mobilized human CD34+ stem cells obtained from blood, after 14 days of culture in serum-free hybridoma medium supplemented with IL-3, IL-6, SCF, and β-mercaptoethanol the human peripheral blood CD34+ cells were switched to STEMdiff Neural Induction medium (STEMCELL Technologies, Vancouver, BC, Canada), a medium developed to induce human embryonic stem cells and human induced pluripotent stem cells to become neural stem cells. Cells were cultured in T75 flasks without feeder cells or matrix and remained viable until used on day 4 of culture.
To investigate whether the insulin found in the culture medium of CD34+ stems cells was produced by the stem cells (and not carried over from the medium), cells were cultured using the SILAC metabolic labeling system (ThermoFisher Scientific) containing 13C-leucine. Culture supernatants were collected and centrifuged for analysis by mass spectrometry.
Mouse CD34+ stem cells were cultured from peripheral blood buffy coats in 10 ml GIBCO DMEM/10% fetal bovine serum supplemented with 10 ng/ml mouse IL-3, 5 ng/ml mouse IL-6, 10 ng/ml mouse SCF, and β-mercaptoethanol, the growth medium developed to grow CD34+ hematopoietic progenitors from adult mouse bone marrow. The cells were cultured in T75 tissue culture flasks as reported  with only suspension cells being retained at each passage with 2 × 106 suspension cells being replated in a new T75 flask. No feeder cells or matrix were employed.
Quantitative polymerase chain reaction
Primers used for quantitative polymerase chain reaction
CD34 (99 bp)
Neurofilament-H (149 bp)
Oct 4 (96 bp)
Pdx 1 (109 bp)
Pax 6 (98 bp)
MOG (107 bp)
Tuj-1 (112 bp)
cKit (109 bp)
Villin (95 bp)
SOX-2 (76 BP)
LIN-28 (97 BP)
NG2 (102 bp)
PLP (111 bp)
PTF 1a (75 bp)
GAPDH (96 bp)
β-Actin (92 bp)
Immunocytochemistry was carried out by standard methodology using the following antibodies: CD34 (Pharmingen, 553731), cKit (Cymbus Biotechnology, CBL1359), CD45 (Pharmingen, 553076), Oct-4 (Santa Cruz, sc-9081), Sox-2 (Santa Cruz, sc-20088), LIN28 (Santa Cruz, sc-67266), Pax-6 (Santa Cruz, sc-11357), neurofilament H (Sternberger Monoclonals, SMI 312), Tuj1 (Covance, PRB435P and MMS435P), PLP (Chemicon, MAB388), NG2 (Chemicon, AB5320), MBP (from BP), MOG (Millipore, MAB345), Pdx1 (Chemicon, AB3243), Ptf1α (R&D Systems, AF6119), glucokinase (Santa Cruz, sc7908), insulin A (Santa Cruz, sc-7839), insulin B (Santa Cruz, sc-7838), and villin (Santa Cruz, sc-7672).
Immunofluorescence staining was performed according to the methods given in the Supplemental Materials and Methods (Additional file 1).
Western blot analysis
Western blot analyses were conducted via standard methodology using the antibodies listed above in section 2.4 (Immunocytochemistry).
Analysis of insulin peptides from human mobilized CD34+ stem cells grown in protein-free medium
Mass spectrometry was performed by the Protein Analysis Laboratory, Center for Vascular and Inflammatory Diseases, University of Maryland School of Medicine. The proteins from the conditioned media were captured by solid-phase extraction using TARGA C18 MicroSpin tips (The Nest Group, Southborough, MA, USA). After acidifying the conditioned media with trifluoroacetic acid to a final concentration of 0.1%, it was passed through the MiniSpin tips, washed with 10 column volumes of 0.1% trifluoroacetic acid, and proteins were eluted with 70% acetonitrile containing 0.1% trifluoroacetic acid. The eluted fraction was evaporated to dryness in a centrifugal evaporator and subsequently dissolved in 100 μl 100 mM triethylammonium bicarbonate, pH 8.5, containing 2% sodium deoxycholate. Disulfide bonds were reduced with 5 mM dithiothreitol at 37 °C for 30 min followed by alkylation of the sulfhydryl groups with chloroacetamide at room temperature in the dark. After neutralization of residual chloroacetamide by the addition of DTT, proteins were digested overnight at 37 °C with Trypsin/LysC (Promega, Madison, WI, USA) at a final concentration of 12.5 ng/μl of the enzyme mixture. The digested sample was acidified with trifluoroacetic acid to a final concentration of 1% and the precipitated sodium deoxycholate was removed by centrifugation at 10,000 × g for 5 min. The peptides were recovered from the supernatant by solid-phase extraction using the TARGA C18 MicroSpin tips as described above and subsequently analyzed by liquid chromatography tandem mass spectrometry (MS/MS). Peptides were separated by reversed phase high-performance liquid chromatography (HPLC) on an in-house pulled-tip fused silica (Molex PolyMicro Technologies) capillary column (0.1 mm × 150 mm) packed with TARGA C18 3 μ stationary phase connected to a Surveyor HPLC pump (Thermo Scientific) operated at 200 μl/min and set up to deliver a split flow to the capillary column at ~ 0.45 μl/min. Electrospray was initiated by application of 1800 V at the head of the column via a liquid junction. Gas phase ions were analyzed in an LTQ Orbitrap mass spectrometer (Thermo Scientific) using a duty cycle of one full scan followed by MS/MS scans on up to 12 of the most abundant ions, above a preset threshold, observed in the preceding full scan. These data were analyzed with Proteome Discoverer 1.4 (Thermo Scientific) using the Sequest HT search engine to match acquired spectra against a human subset of the Uniprot protein sequence database, which included sequences of common protein contaminants. Percolator was used to validate peptide-spectrum matches at a Q value  (false discovery rate (FDR)) of 0.01.
Analysis of insulin peptides labeled with 13C-leucine from human mobilized CD34+ stem cells grown in SILAC medium
Mass spectrometry was performed at the University of Maryland School of Pharmacy Mass Spectrometry Center. Tryptic peptides were separated on a Waters nanoACQUITY UPLC system with a 20-cm ACQUITY UPLC M-Class CSH C18 column by a 3–43% acetonitrile gradient in 0.1% formic acid over 180 min at a flow rate of 400 nL/min, and were analyzed on a coupled Thermo Scientific Orbitrap Fusion Tribrid mass spectrometer as described . Tandem mass spectra were searched against human insulin chain A and chain B sequences using SEQUEST HT algorithm with a precursor tolerance of 5 ppm and a product tolerance of 0.5 Da. 13C-labeled leucine was treated as a variable modification, and cysteine carbamidomethylation was treated as a fixed modification.
A subset of mobilized human and mouse CD34+ stem cells grow exponentially in vitro
Differences in CD34+ stem cells between human and mouse peripheral blood
We were able to culture CD34+ stem cells from mouse peripheral blood buffy coat, but we were not able to grow CD34+ bone marrow stem cells from commercial human nonmobilized blood buffy coat or from purified human nonmobilized peripheral blood mononuclear cells. We were able to culture CD34+ stem cells from mobilized human peripheral blood (Fig. 1). The CD34+ stem cell cultures from mobilized human peripheral blood differed from those obtained from the mouse in that, while the latter contained a single spherical cell morphology, the former contained four morphological phenotypes: one cell type that was adherent to the plastic flask, and three cell types that grew in suspension—a spherical cell, a cone-shaped cell, and a minute cell. All four cell types persisted throughout the culture period, although only the nonadherent cells were passaged in culture. The three nonadherent subtypes were harvested for analysis in the experiments that followed.
Gene expression by a subset of mobilized human peripheral blood CD34+ cells
Western blot analysis of protein expression by a subset of human mobilized CD34+ bone marrow stem cells
Human and mouse mobilized CD34+ stem cells uniformly express ESC and germ layer lineage genes in vitro
Gene expression in a subset of human peripheral blood CD34+ can be modulated by culture conditions
A subset of human mobilized CD34+ stem cells synthesize insulin
The potential of stem cells as cell replacement therapy for degenerative disease and other types of tissue injury has been complicated by the ethical issues surrounding the use of embryonic stem cells , the histocompatibility issues of tissue-specific stem cells from other individuals , the difficulty obtaining large quantities of inducible pluripotent stem cells , and teratoma formation by both embryonic and inducible pluripotent stem cells . Early reports from mouse studies and studies of human transplant recipients suggesting the possibility that hematopoietic stem cells could transdifferentiate into cells of other types including neural cells [17–21], cardiac cells [22–24], hepatic cells [25–28], and pancreatic cells [29, 30] sparked interest in hematogenous stem cells for cell replacement therapy. Subsequently a population of very small embryonic-like (VSEL) stem cells was identified as a possible circulating pluripotent stem cell [31, 32]. More recently, this enthusiasm has been tempered by evidence that at least some of the observations were due to cell fusion , the presence of CD34 antigen on progenitor cells not of hematogenous origin , and the failure to confirm the findings regarding VSEL stem cells . While we were able to exclude cell fusion as an explanation in our earlier work suggesting that CD34+ stem cells could transdifferentiate into multiple lineages when placed into mouse blastocysts , in studies showing transdifferentiation into oligodendroglial cells which ensheath axons in Shiverer mice  we did not fully exclude the possibility of cell fusion. We did identify a small cell morphology in cultured cells from mobilized human blood that might correspond with the previously reported VSEL stem cells , but we did not attempt to separate or test the cells separately with that morphology. Therefore, it was important to demonstrate that gene expression by the CD34+ cells can be modulated (in this case by culture conditions) and that the CD34+ cells express genes characteristic of differentiated tissues (in this case insulin). The current results show both that gene expression by the CD34+ cells can be modulated by culture conditions and that the CD34+ cells can translate and transcribe the gene for insulin in conditions where cell fusion with pancreatic cells was not possible. These findings support the idea that this subpopulation of CD34+ stem cells might either be at a stage prior to commitment to the hematogenous lineage or be capable of transdifferentiation from that lineage to other lineages. Further work is needed to determine this.
If these CD34+ stem cells are shown to be capable of differentiating into other cells types, then the practical issue of their availability would be important. We have shown previously that, although the cells could be obtained from mouse bone marrow and peripheral blood, we could obtain them from human bone marrow but not peripheral blood. Our results in the current study showing that the cells can be obtained from mobilized peripheral blood would allow for a practical method for obtaining large numbers of cells should they be found useful in cell replacement therapy or for other purposes.
Mobilized human CD34+ bone marrow stem cells constitutively express an array of ESC and embryonic germ layer lineage genes. Gene expression can be modulated by modifying culture conditions, and the cells synthesize insulin. These results suggest a practical source of autologous stem cells for studies to determine whether they might be useful in cell replacement therapy.
The authors would like to thank Deborah Yarnell for technical assistance and Mohammed I. Arvas for his assistance with manuscript revisions.
This work was supported by funding from the Department of Veterans Affairs to PSF and CTB. Additional support was provided by the University of Maryland, School of Pharmacy Mass Spectrometry Center (SOP1841-IQB2014).
Availability of data and materials
Data will be made available according to the Department of Veteran’s Affairs policies on data use and sharing.
BP and DT designed the study; TM, PSF, BP, CTB, and DT provided resources for the study; TM, VKN, PRG, BH, WH, MAK, and DT performed the experiments; TM, CTB, BH, WH, MAK, and DT analyzed the data; TM, BH, WH, MAK, PSF, CTB, and DT co-wrote the manuscript. All authors reviewed the galley proofs and, with the inclusion of the corrections I am submitting now, have approved the final manuscript.
All procedures were performed in accordance with an approved University of Maryland School of Medicine Institutional Animal Care and Use Committee Protocol. National Institutes of Health guidelines for animal treatment and care were followed assiduously.
DT and CTB hold US (US 8,940,535 B2) and International (PTC/US04/37122) patents.
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