For decades, in vitro expansion of transplantable hematopoietic stem cells (HSCs) has been an elusive goal. Here, we demonstrate that multipotent adult progenitor cells (MAPCs), isolated from green fluorescent protein (GFP)-transgenic mice and expanded in vitro for >40–80 population doublings, are capable of multilineage hematopoietic engraftment of immunodeficient mice. Among MAPC-derived GFP+CD45.2+ cells in the bone marrow of engrafted mice, HSCs were present that could radioprotect and reconstitute multilineage hematopoiesis in secondary and tertiary recipients, as well as myeloid and lymphoid hematopoietic progenitor subsets and functional GFP+ MAPC-derived lymphocytes that were functional. Although hematopoietic contribution by MAPCs was comparable to control KTLS HSCs, approximately 103-fold more MAPCs were required for efficient engraftment. Because GFP+ host-derived CD45.1+ cells were not observed, fusion is not likely to account for the generation of HSCs by MAPCs.
Hematopoietic stem cells (HSCs) reside predominantly in the BM and can be purified to near homogeneity based on their c-Kit+, Thy1.1low, hematopoietic lineage marker negative (Lin−), Sca-1+ phenotype; i.e., KTLS cells (1, 2). HSCs efficiently repopulate the hematopoietic system of primary recipients, and purified donor-derived KTLS cells from engrafted mice robustly reconstitute secondary hosts. The ability to expand or generate HSCs ex vivo would greatly facilitate the development of novel therapies for hematopoietic disorders for which no current therapy exists, or where numbers of available HSCs are insufficient. Although improvement of in vitro HSC expansion or generation of HSCs from embryonic stem cells (ESCs) might provide a solution, both are at early stages of research. Furthermore, for ESC-derived HSCs to be safe in transplantations, they must be free of residual teratogenic cells (3–6). Aside from HSCs, the BM contains at least one other multipotent stem cell population, mesenchymal stem cells. The contribution of HSCs is restricted to hematopoietic cells, whereas mesenchymal stem cells appear limited to muscle, cartilage, bone, and fat differentiation (7, 8). Although rare cells have been postulated to contribute to both hematopoietic and nonhematopoietic cells, “donor-derived” tissues often express both donor and host markers (9–14).
Recently, numerous groups have isolated nonhematopoietic cell populations from the BM or umbilical cord blood via in vitro culture, which appear able to differentiate into cells with mesodermal, endodermal, and ectodermal characteristics (15–17). In previously published studies, we demonstrated that it was possible to isolate a clonal population of cells, named multipotent adult progenitor cells (MAPCs), from murine BM that contributes to all three germ layers upon injection into blastocysts (18, 19). MAPCs differentiate into various lineages in vitro using defined cytokine combinations, and when transplanted into sublethally irradiated nonobese diabetic (NOD)-SCID mice, they contribute at low levels to hematopoietic and some endodermal tissues (19). Reyes et al. (20) recently reported that MAPC-like cells can be transferred from donor to host after whole BM transplantation, potentially explaining the plasticity of many BM-derived populations (12, 21, 22).
Since the initial description of MAPCs, we improved MAPC isolation and expansion conditions (23). MAPC clones isolated using improved protocols express Oct4 (a transcription factor required for undifferentiated ESC maintenance; reference 24) at levels approaching those of ESCs. However, MAPCs do not express two other transcription factors known to play a major role in ESC pluripotency, Nanog and Sox2 (25–27). These Oct4-expressing MAPCs differentiate more robustly in vitro to mesodermal and endodermal cell types as compared with MAPCs described previously (unpublished data). Here, we demonstrate that MAPC populations contribute to hematopoiesis in vivo and may precede HSCs in ontogeny given that they generate long-term repopulating HSCs (LT-HSCs) and the full repertoire of hematopoietic progenitors.
Characteristics of Oct4high MAPCs
MAPCs were derived under low oxygen (O2) conditions (23) from the BM of two independent C57BL mouse strains that express enhanced GFP (eGFP) under control of the β-actin promoter. Only MAPC clones that expressed Oct4 at levels ≥20% of the R1 murine ESC line and stained positive with an anti-Oct4 antibody (Fig. S1) were used for subsequent studies. Because Oct4 levels vary upon long-term passage, cell aliquots were analyzed for Oct4 mRNA expression at the time of transplantation (Table S1). Phenotypically, MAPCs were CD31, CD44, CD45, CD105, Thy1.1, Sca-1, E-cadherin, MHC class I and II, as well as hematopoietic lineage marker negative, and expressed low levels of EpCAM and high levels of c-Kit, VLA-6, and CD9 (Fig. S2). Furthermore, low O2-derived MAPCs did not express detectable transcripts of the hematopoietic-specific transcription factors Lmo2, Scl, Gata2, Ikaros, or Pu.1.
Long-term multilineage hematopoietic repopulating activity of MAPCs
Initial attempts to transplant 106 MAPCs into lethally irradiated C57BL mice failed due to pancytopenia. We next transplanted MAPCs into sublethally irradiated NOD-SCID mice that also received anti–asialo-GM1 antibodies to deplete recipient NK cells (28). 3 wk after transplantation of 0.3–1 × 106 MAPCs, ∼5% GFP+CD45.2+ donor cells could be detected in the blood. The percentage of GFP+ cells increased substantially by 6–8 wk and continued to increase until 20 wk after transplantation. Engraftment (≥1% GFP+CD45.2+CD45.1− cells) was observed in 19/26 and 2/2 mice transplanted with MAPC clone DDD and G6, respectively, 3–21 wk after transplant (Tables I and S1).
MAPCs transplanted in the 21/28 mice that engrafted were <35% hypodiploid or hyperdiploid, and expressed Oct4 mRNA between 13 and 100% of that observed in mouse ESCs (mESCs; Table S1). Of the seven mice that did not show hematopoietic engraftment, two animals received cells that were 95% aneuploid. Of note, animals transplanted with euploid cells or aneuploid cells did not develop tumors with posttransplant follow-up of 21 wk. Furthermore, cytogenetic analysis on peripheral blood (PB) of MAPC-transplanted mice also showed a normal karyotype (Table S3). Of the remaining five animals that were not reconstituted, three received MAPCs that expressed Oct4 mRNA at levels 2% of mESC, and two animals showed no engraftment despite transplantation with 75 and 90% of euploid cells expressing 52 and 55% Oct4 mRNA (vs. mESC), respectively.
Although the degree of hematopoietic contribution from MAPCs varied, chimerism of primary recipients was maintained until mice were killed as late as 24 wk after transplant. GFP+ cells in the BM, spleen, PB, and LNs appropriately expressed markers for B lymphocytes, T lymphocytes, or myeloid cells (Fig. 1). In the spleen and PB of long-term engrafted mice, we also detected GFP+ dendritic cells, NK cells, and megakaryocytes (Fig. S3). The majority of GFP+ cells in BM obtained between 3 and 10 wk after transplantation were Mac-1+/Gr-1+ double positive, although B and T lymphocytes could be detected (Fig. S4). Between 11 and 21 wk after MAPC infusion, lymphoid repopulation increased, thereby confirming stable, long-term multilineage reconstitution (Fig. S4).
We next evaluated the fraction of animals that engrafted with lower doses of MAPCs (3 × 104 to 106 cells/mouse) to assess the minimal dose of MAPCs required to establish long-term, stable chimerism (Table I). Hematopoietic reconstitution of all lineages was observed in one out of five mice injected with 3 × 104 MAPCs and in three out of six mice injected with 105 cells, suggesting that the minimal dose of MAPCs needed for hematopoietic reconstitution is ∼50,000 cells.
To directly compare MAPC-based contribution to hematopoiesis with KTLS HSCs, we co-transplanted 600 KTLS cells or 7.5 × 105 MAPCs from β-actin GFP mice with 0.2–1 × 106 Sca-1–depleted CD45.1+ BM cells in sublethally irradiated NOD-SCID mice. Hematopoietic reconstitution by MAPCs was similar to KTLS cells, and the repertoire of hematopoietic engraftment by MAPCs versus KTLS cells was virtually indistinguishable (Fig. 2).
Several studies have suggested that unexpected contribution of adult stem cells to tissues other than the lineage of origin may be due to fusion of donor cells with host cells (8, 30–32). In all mice analyzed, we never detected CD45.1+CD45.2+ or CD45.1+GFP+ cells, suggesting that fusion between donor (CD45.2+GFP+) MAPCs and recipient (CD45.1+) cells does not contribute to hematopoietic reconstitution (Figs. 1 and 2). CD45.1+GFPdim cells were present in both MAPC and KTLS transplants, but these cells were all Mac1+ and represent host-derived macrophage engulfment of donor-derived GFP+ cells (not depicted).
Self-renewal capacity of MAPC-derived HSCs
Within the GFP+CD45.2+CD45.1− BM cells of primary recipients, we could detect 1–2% ckit+Sca-1+Lin− (KLS) and ∼0.1% ckit+Lin−Sca-1+Flk2− (KLSFlk2−) cells. This suggested in vivo generation of LT-HSCs from MAPCs (Fig. 3 A; reference 29).
To determine whether functional LT-HSCs were generated by MAPCs, we evaluated whether MAPC-derived cells from primary recipients could stably reconstitute secondary mice. In an initial set of experiments, 106 total BM cells from primary recipients of MAPCs or KTLS cells at 16–20 wk after transplant were transferred to five lethally irradiated NOD-SCID or C57BL-CD45.1+ mice. Three out of five NOD-SCID and three out of five C57BL mice that received BM from MAPC-engrafted mice, and two out of five NOD-SCID and five out of five C57BL mice transplanted with KTLS progeny survived to week 8 after transplantation. All surviving secondary mice had high levels of GFP+CD45.2+ multilineage hematopoiesis at 24 wk after transplant (Fig. 3 B). Furthermore, similar levels of donor-derived LT-HSCs (KLS Flk2−CD34−) and all hematopoietic progenitor populations were present in the BM of C57BL secondary recipients of KTLS- and MAPC-derived BM cells (Table II and Table S5; reference 30). Similar results were observed in a second experiment where total mononuclear cells (106 cells/mouse, n = 6) and CD45+ selected cells (106 cells/mouse, n = 9) were transplanted from a primary MAPC-engrafted recipient, and long-term GFP+CD45.2+ hematopoietic reconstitution was detected in secondary recipients (Table III).
To more clearly demonstrate that MAPCs generate LT-HSCs, we isolated GFP+KTLS cells from MAPC-engrafted animals and transplanted these into secondary recipients. Co-transplantation of 200 GFP+KTLS cells with 106 Sca-1–depleted BM cells into lethally irradiated mice resulted in the establishment of long-term GFP+ hematopoiesis in three out of four NOD-SCID and four out of four C57BL mice (Table III). We further established the generation of functional MAPC-derived HSCs and their downstream progenitors by demonstrating that these cells could both radioprotect and establish long-term hematopoiesis. To do this, we transplanted 2 × 103 GFP+ KLS cells without Sca-1–depleted cells. This resulted in robust GFP+CD45.2+ hematopoietic reconstitution in two out of three mice, and multilineage reconstitution that persisted in all secondary recipients until they were killed at weeks 15–24 (Table III).
BM obtained 16 wk after transplant from secondary recipients that received 2 × 103 MAPC-derived GFP+ KLS cells contained 0.8–1.3% GFP+ KLS cells (not depicted). When 106 total BM cells from these secondary recipients were transplanted in 10 lethally irradiated tertiary C57BL mice, 4–37% GFP+CD45.2+ chimerism was seen in the seven tertiary surviving mice 1 mo after transplantation. At 3 mo, two out of seven animals showed GFP+CD45.2+ chimerism (2.7 and 70%), but engraftment was skewed toward the myeloid lineage. In a separate experiment, of the three NOD-SCID mice that received 106 BM cells from secondary mice that had received total BM cells from primary MAPC- or KTLS-grafted animals, two out of five KTLS- and one out of five MAPC-derived tertiary recipients remained alive 3 mo after transplant, with multilineage chimerism levels of 8 ± 0.9% and 11.5% in surviving mice, respectively.
Immune reconstitution by MAPC-derived hematopoietic cells
That MAPCs generate lymphoid cells was first observed using intravital microscopy, demonstrating obvious GFP fluorescence in all lymphoid organs, including the thymus, spleen, and LNs (Fig. 4 A). This was confirmed by flow cytometry, where mature B and T lymphocytes were detected in all organs analyzed (Figs. 1, 4, and S4). In addition, histopathology of mesenteric LNs demonstrated that MAPC-derived T and B cells can form normal primary follicles (Fig. 4 B).
The thymus of six NOD-SCID mice 6–20 wk after transplant with 106 MAPCs were shown to contain 23 ± 16.5 × 106 cells (1–50 × 106), of which 73 ± 35.3% (5–99%) were GFP+CD45.2+ (Fig. 4 C). GFP+CD45.2+ cells constituted major portions of the double-negative, double-positive, and CD4 and CD8 single-positive populations (Fig. 4 D). Moreover, >50% of single GFP+CD4 or GFP+CD8 T cells expressed the TCR-β, as would be anticipated for mature thymocytes before emigration into the periphery. All four stages of triple-negative thymocytes were also represented (Fig. 4 E). Finally, mature T cells were present in inguinal LNs (Fig. 1).
To test lymphoid cell function, we examined the in vitro response of MAPC-derived CD4/CD8 cells to TCR-CD3/CD28-mediated signals. The level of [3H]thymidine incorporation was similar in splenic T cells from MAPC-engrafted versus control GFP-transgenic mice 3–7 d after stimulation (Fig. 4 F). Serum of NOD-SCID mice not grafted with MAPCs had detectable levels of IgM, but not IgG2. In contrast, we detected both IgG2 and IgM in the serum of MAPC-engrafted mice (n = 6), demonstrating normal B and T cell function, as an antibody class switch from IgM to IgG2 had occurred (Table IV).
Of note, a single animal developed clinical and pathological features indicative of severe chronic graft-versus-host disease (GVHD) 16 wk after transplantation with 0.6 × 106 MAPCs. Tissue histopathology showed chronic GVHD of the skin, along with severely damaged bile ducts in the liver and severe lung damage (Fig. 5). In areas of chronic GVHD-induced injury (not depicted), donor T cells were predominantly CD3+CD4+, with lesser numbers of CD3+CD8+ T cells.
Engraftment in other tissues
We also evaluated engraftment in tissues other than the lymphohematopoietic organs with the primary purpose of assessing extrahematopoietic contribution, and secondarily to investigate whether microscopic tumors were formed. In all sections analyzed, neither microscopic nor macroscopic tumors were observed. All GFP+ cells in the tissues analyzed from KTLS-transplanted mice were hematopoietic in origin (i.e., CD45+), confirming no extrahematopoietic contribution by HSCs (14). In MAPC-transplanted animals, GFP+ cells were readily detectable in the brain, muscle, liver, lung, and gut, but the vast majority of these cells were also CD45+. Among the GFP+ cells that did not co-label with hematopoietic markers, we found no evidence for neural, astrocytic, oligodendrocyte, or epithelial differentiation. The nature of these GFP+CD45− cells is currently unclear. In three animals, we detected rare individual GFP+ cells within the heart that were striated and costained with anti-cardiac troponin-I antibodies (not depicted). The low frequency of this event is consistent with cell fusion (9, 14), although these cells were not detectable in KTLS-transplanted animals. This would suggest that this contribution is specific to MAPCs, but at the moment we cannot speculate on the possible explanation for this phenomenon.
In BM, multiple populations of stem and progenitor cells exist with defined potential. The best characterized of these is the HSC, which gives rise to all hematopoietic lineages. Aside from HSCs, BM also contains other multipotent cells, including mesenchymal stem cells. Several recent studies have suggested that more primitive cells may exist in the BM or umbilical cord blood, with differentiation potential toward mesodermal, endodermal, and ectodermal fates, including MAPCs (15–19, 31). Each of these populations is purified using in vitro culture techniques, and it remains to be determined whether they exist in vivo.
We previously demonstrated that clonally derived MAPCs contribute to hematopoiesis in a transplant setting (19). However, contribution was low (2–8%) and progeny were not thoroughly characterized. Here, we show that clonally derived MAPCs functionally reconstitute the hematopoietic system in vivo and generate HSCs and their progenitor cell populations, which robustly contribute to multilineage engraftment in primary and secondary irradiated recipients. MAPCs alone were not radioprotective, despite the fact that the hematopoietic progeny they generated in vivo are radioprotective. Thus, undifferentiated MAPCs cannot be used for transplantation as the sole source of hematopoiesis in lethally irradiated recipients, but can reconstitute long-term hematopoiesis. Consistent with the high levels of hematopoietic reconstitution by MAPCs, we could detect GFP+ cells in all organs analyzed, although most GFP+ cells coexpressed CD45. Expression of tissue-specific markers in GFP+ cells was only observed in the heart. The low frequency of this event, and fusogenic properties of cardiac muscle fibers, suggests that this may result from fusion (9, 14). In other tissues, rare GFP+ cells that did not co-label with hematopoietic markers also did not stain with antibodies against tissue-specific proteins. The nature of these is currently under investigation.
Arguably, hematopoietic engraftment cannot be explained by contamination of the graft by HSCs, as MAPCs were expanded for 40–80 population doublings over 3–5 mo in vitro. If rare contaminating HSCs were responsible for the results observed here, HSC expansion for this period of time and to a level of >108–1012-fold would be unprecedented for an in vitro culture system. Moreover, MAPCs are derived from BM depleted of CD45+ cells, do not express detectable CD45, Sca-1, Thy1.1, Mac1, Gr1, CD3, CD4, CD8, B220, and Ter119, and do not express HSC-specific transcription factors Scl, Lmo2, Gata2, Ikaros, and Pu.1 (quantitative RT-PCR and gene array analysis [data are available in the GEO database under accession numbers GSE5947 and GSE6291]; not depicted).
Although several studies initially suggested that adult BM stem cells may be capable of acquiring a lineage fate different from the tissue of origin in vivo, several studies have now demonstrated that such plasticity is not cell autonomous but due to fusion between BM-derived cells and cells in the target organ (9, 10, 13, 32, 33). Fusion events characteristically occur infrequently and do not significantly contribute to tissue unless the fused cell has a proliferative or survival advantage over nonfused cells (10). Furthermore, fused cells usually express some markers of both the host and donor cell. To address whether fusion might explain our observations, we used CD45-congenic animals in addition to using donor cells universally expressing GFP. In no instance did we observe coexpression of CD45.1 with CD45.2 or GFP, except in the case of host Mac1+GFPdim cells that represent host macrophage engulfment of donor-derived cells (Fig. 2 B), making the high level of hematopoietic reconstitution observed after MAPC engraftment extremely unlikely due to fusion.
Numerous advances in MAPC isolation, culture, and transplantation likely explain the significantly greater hematopoietic reconstitution observed after transplantation in this study versus our previous attempts (19). First, we conditioned sublethally irradiated NOD-SCID mice with an anti–NK cell antibody. Although NOD-SCID mice do not have functional B or T cells, they do have robust NK cell activity, which mediates rejection of grafted cells (34). For instance, engraftment levels of human SCID-repopulating cells are significantly enhanced when human CD34+ cells are transplanted in NOD-SCID-IL2Rγc−/− or NOD-SCID-β2M−/− mice, or NOD-SCID mice treated with an anti-CD122 antibody (34). We recently showed that a substantial fraction of murine MAPCs, which are MHC class I low, are rejected early after transplantation in NK-competent animals, leading to significantly lower levels of long-term engraftment compared with transplantation into NK-deficient animals (28). Murine ESC-derived HSCs, which, like MAPCs, are MHC class I low, also yield significantly higher levels of hematopoietic engraftment when transplanted into animals that are NK deficient (4).
Second, MAPCs used in this study were derived using improved methodology (23). Compared with previously generated MAPCs, those derived using 5% O2 express ∼103-fold higher mRNA levels of the ESC-specific transcription factor Oct4 (24). We have evidence that the higher level of Oct4 transcripts is associated with a significantly broader and more robust differentiation ability of MAPCs to several mesodermal and endodermal lineages in vitro (unpublished data).
Not surprisingly, MAPCs were unable to radioprotect lethally irradiated C57BL mice and require co-transplantation of Sca-1–depleted BM to prevent death from pancytopenia early after transplantation. Because myeloid reconstitution is delayed upon transplant of highly purified HSCs into lethally irradiated mice, it is well established that co-transplantation of Sca-1–depleted BM cells is needed to transiently protect animals until mature blood lineages develop (35). The notion that MAPCs are unable to radioprotect is consistent with the hypothesis that MAPCs precede HSCs during ontogeny, and that commitment to an HSC fate might be required before establishing hematopoiesis. The presence of KLS Flk2− cells (29), robust engraftment of secondary recipients by MAPC-derived GFP+ KTLS, and radioprotection as well as long-term hematopoietic reconstitution by GFP+ KLS cells demonstrates that LT-HSCs are, in fact, generated by MAPCs.
Compared with freshly isolated KTLS cells, significantly more MAPCs are required to establish hematopoiesis. This incongruity likely reflects several differences between the two cell types. First, it is possible that the efficiency of MAPC commitment to LT-HSCs is poor. Second, and most notably, the efficiency of MAPC homing and engraftment in BM niches is, as yet, unknown. In contrast to KTLS cells, MAPCs, aside from Tie2 (36), do not express Cxcr4, Itga4 and Itga5, Pecam1, Cd44, or Cd164 (gene array analysis [data are available in the GEO database under accession numbers GSE5947 and GSE6291]; not depicted and references 37–41). This constellation of chemokine and adhesion receptors is known to play a critical role in HSC homing and engraftment, and its absence may contribute to the lower engraftment efficiency of MAPCs versus KTLS cells.
Nevertheless, MAPC-derived progenitors were capable of migrating to the thymus, where they underwent typical differentiation processes as demonstrated by intravital microscopy, flow cytometry, and tissue immunohistochemistry. Peripheral B and T cell reconstitution of the spleen and LNs was intact. Serum Ig levels and IgG2a isotype switching were indicative of successful B cell–T cell interactions. In vitro T cell responses to CD3 and CD28 signals were intact, and in one mouse, donor T cells were sufficiently mature to mount a chronic GVHD response as confirmed by clinicopathological analysis and the presence of mature T cells in GVHD target organs. We do not know the inciting factors for chronic GVHD development in this mouse, but possibilities include failed thymic negative selection, inadequate peripheral tolerance mechanisms, and/or the presence of a pathogen (e.g. virus) that might break existing tolerance. Future studies measuring in vivo responses to foreign antigens will be required to quantify the extent of functional B and T cell responses. Nonetheless, these data demonstrate the capacity of MAPC-derived HSCs to reconstitute irradiated recipients with a functional lymphoid system.
In conclusion, we demonstrate that MAPC cultures can robustly contribute to hematopoiesis in vivo while generating functional lymphoid cells and serially transplantable HSCs, but they do not generate observable microscopic or macroscopic tumors, an important trait when considering their therapeutic utility. Because MAPCs can be expanded for prolonged periods ex vivo without evidence of senescence and can be easily genetically manipulated, they may prove invaluable for the treatment of inherited hematopoietic disorders. Given that MAPCs can differentiate to mesoderm, endoderm, and ectoderm in vitro (42–44), and to the extent that they may be better adapted to do so in vivo given the proper environment, MAPCs may greatly facilitate tissue repair in vivo through the establishment of hematopoietic chimerism as a means to induce transplantation tolerance and, therefore, successful transplantation of MAPC-derived tissue-committed cells without immune-mediated rejection (45, 46).
Materials And Methods
Mice carrying the eGFP gene were provided by M. Okabe (Osaka University, Osaka, Japan; C57BL/6TgN(act-EGFP) ObsC14-Yo1-FM1310) and by I.L. Weissman (C57BL/Ka-CD45.2+-eGFP). Both strains use the β-actin promoter to encode for eGFP, and eGFP expression is present in >95% of all tissue cells. NOD/LtSz-scid/scid (NOD-SCID) and C57BL/6 (CD45.1+) mice were purchased from The Jackson Laboratory. Mouse colonies were established at the University of Minnesota for the C57BL/Ka-CD45.2+-eGFP, C57BL/6TgN(act-EGFP) ObsC14-Yo1-FM131, and NOD-SCID mice. All mice were housed under specific pathogen-free conditions. All protocols involving mice were approved by the Institutional Animal Care and Use Committee at the University of Minnesota and Stanford University.
MAPC culture and characterization.
MAPCs were isolated from the BM of C57BL/6TgN (act-EGFP) ObsC14-Yo1-FM131 mice (clone G6) and C57BL/Ka-CD45.2+-eGFP mice (clone DDD), as described previously (19, 23). In brief, BM was plated in DMEM/MCDB (Invitrogen) containing 10 ng/ml EGF (Sigma-Aldrich), PDGF-BB (R&D Systems), and LIF (Chemicon International), 2% FCS (Hyclone), 1× selenium-insulin-transferrin-ethanolamine, 0.2 mg/ml linoleic acid-bovine serum albumin, 0.8 mg/ml bovine serum albumin (all from Sigma-Aldrich), 1× chemically defined lipid concentrate (Invitrogen), and 1× α-mercaptoethanol (Invitrogen) in a humidified 5% O2 and 6% CO2 incubator. After 4 wk, CD45+ and Ter119+ cells were depleted using a MACS separation CS column (Miltenyi Biotec) and plated at 10 cells/well. Clones consisting of cells with Oct4 mRNA levels >20% of mESC (R1 cells, maintained on murine embryonic fibroblasts) were expanded and used for the studies described.
Approximately monthly, MAPCs were analyzed by FACS for cell surface phenotype. Samples were stained with the following fluorochrome- conjugated antibodies: Sca-1 (E13-161.7); c-kit (2B8); Thy1.1 (OX-7); CD44 (IM7); MHC-Ib (H2b, AF6-88.5); MHC-IIb (IAb, AF6-120.1); CD31 (MEC13.3); CD3 (145-2C11); B220 (RA3-6B2); Mac1 (M1/70); Gr-1 (8C5); and isotype-PE and APC antibodies. For CD45.2 (104) and CD9 (KMC8) staining, a biotinylated antibody was used, followed by streptavidin and APC. Cells were stained with purified antibody against E-cadherin (ECCD-2; Takara Bio Inc.); EpCAM (G8.8); CD105 (MJ7/18); and CD49f (G0H3). An APC-conjugated goat anti–rat IgG F(ab')2 antibody (Jackson ImmunoResearch Laboratories) was used as secondary antibody. All antibodies were from BD Biosciences unless otherwise noted.
Within 1 wk of transplantation, Oct4 transcripts and/or Oct4 protein levels were evaluated by quantitative RT-PCR and immunoperoxidase staining, respectively (for primers see Table S2). Transcript levels for the hematopoietic transcription factors Gata-2, Scl, Lmo2, Pu.1, and Ikaros were evaluated by quantitative RT-PCR (for primers see Table S2). MAPCs were subjected within 1 wk before transplantation to cytogenetic analysis as described previously (23). Results of quantitative RT-PCR for Oct4 and cytogenetic analysis of cells used in the studies described are provided in Table S1.
Intermittently, cells were subjected to trilineage (endothelium, hepatocyte, and neuroectodermal) differentiation to prove multipotency of the cell populations used (19, 42). Differentiation was confirmed when transcript levels for Sox-1, Otx-1, nestin, and NF200 increased at least 50-fold, reaching levels 50–500% of those measured in embryonic mouse brain RNA (for primers see Table S1).
KTLS cell isolation.
KTLS (ckit+Sca-1+Thy1.1int/lowLin−) cells were isolated as described previously (1)
MAPC and KTLS cell transplantation.
For primary grafts, 6–8-wk-old NOD-SCID mice were irradiated with 275 cGy/min at 57 cGy/min. 4 h before injection of MAPCs, NOD-SCID mice were treated with an intraperitoneal injection of anti-asialo GM1 antibody (20 μL of the stock solution diluted in 380 μL of 1× PBS; Wako Chemicals). The injection of anti-asialo GM1 antibody was also performed after transplantation. Transplantation of MAPCs by tail vein injection occurred 12–24 h after irradiation. KTLS cells were transplanted into NOD-SCID mice after irradiation at 350 cGy. Transplantations of MAPCs or KTLS cells into C57BL-CD45.1+ recipients were performed in lethally irradiated (950–1,000 cGy at 57 cGy/min) animals. KTLS cells, and in some instances MAPCs, were co-injected with 2 × 105–106 Sca-1/CD3-depleted BM cells of host origin. Blood was obtained at different times after transplantation to assess engraftment.
Secondary and tertiary transplants were performed using 106 total BM cells from primary or secondary recipients, respectively. Secondary transplants were also performed using BM CD45+ cells, 2 × 103 cKit+ Sca-1lowLin−GFP+ cells, or 2 × 102 cKit+Sca-1+Thy1.1int/loLin−GFP+ cells isolated by FACS from primary recipients, the latter combined with 106 Sca-1–depleted BM of host background. Cells were either grafted into sublethally irradiated (275–350 cGy) NOD-SCID mice or lethally irradiated (950–1,000 cGy) C57BL-CD45.1+ mice. Blood was obtained at varying times after transplant to follow engraftment. 4–26 wk after transplantation, animals were killed and analyzed for hematopoietic engraftment as described for primary recipients.
Cytogenetic analysis of PB of grafted mice.
Cytogenetic analysis was performed as recommended by The Jackson Laboratory (http://www.jax.org/cyto/blood_preps). Three male NOD-SCID mice were transplanted with MAPCs purified from female C57BL/Ka-CD45.2+-eGFP as described above. In brief, 0.2 ml of blood was collected from the retroorbital sinus of primary recipients into heparinized micro-hematocrit tubes. Cells were stimulated by phytohemagglutinine (final concentration, 7.5 mcg/ml; Invitrogen) and lipopolysaccharide (final concentration, 50 mcg/ml; Sigma-Aldrich) for 42.5 h, treated with cholchicine, and harvested, and metaphases were evaluated according to standard cytogenetic techniques.
Flow cytometric analysis of hematopoietic organs of grafted mice.
Blood samples were obtained at regular intervals by venipuncture. When the mice were killed, hematopoietic organs (BM, PB, spleen, LNs, and thymus) were harvested, single cell suspensions were prepared, and red blood cells were lysed. Cells were analyzed by flow cytometry for the presence of GFP+ donor-derived leukocytes. For FACS analysis, biotinylated or fluorochrome-conjugated mAbs against the following antigens were used: CD45.2, Thy1.1, c-kit, Sca-1, CD3, B220, Mac-1, Gr1, MHC-II (clones as described above), CD45.1 (A20), CD4 (GK1.5), CD8α (53–6.7), TCRβ (H57-597), TCRγδ (GL3), CD19 (1D3), IgM (II/41), CD41 (MWReg30), CD11c (HL3), CD25 (PC61), CD44 (IM7), IL-7Rα (A7R34), Flk2 (A2F10), and FcγR (CD16/32;2.4G2). GFP+CD45.1−CD45.2+ cells were considered donor in origin, and multilineage engraftment was assessed using the markers described above.
Immunohistochemistry for Oct4 on mouse MAPCs and mouse ESCs (clone R1).
Cells were plated at 100 cells/cm2 and stained with goat anti–Oct-3A/4 polyclonal IgG (Santa Cruz Biotechnology, Inc.) or incubated with goat gamma globulin (Jackson ImmunoResearch Laboratories) as negative control. Biotin SP–conjugated anti–goat IgG (Jackson ImmunoResearch Laboratories) was used as secondary antibody. After the secondary antibody, cells were incubated for 30 min with ABComplex-HRP (DakoCytomation) and developed with DAB+ (DakoCytomation) for 2–5 min.
Analysis of donor cell engraftment in tissues by intravital microscopy.
Anesthetized mice (Nembutal) were examined for the presence of GFP+ cells by intravital microscopy as described previously using a stereomicroscope (MZFLIII; Leica) equipped with a GFP2 bandpass filter (Leica) and a Retiga Exi camera with Qcapture software (Qimaging). Exposure times were kept constant for the different organs and, for all mice examined, for objective comparison of GFP fluorescence intensity and any autofluorescence background (47).
To assess T cell responses in vitro, GFP+CD4+ and GFP+CD8+ cells were isolated from the spleens of an engrafted mouse or a control mouse by FACS. 6 × 104 sorted T cells (ratio for CD4/CD8 is 1:1 in MAPC-grafted mouse and control GFP transgenic mouse) were cultured in 96-well plates with anti-CD3 mAb plus anti-CD28 mAb-coated beads (105; provided by C. June and B. Levine, University of Pennsylvania, Philadelphia, PA), and pulsed with tritiated thymidine (1 μCi/well; GE Healthcare) 16–18 h before harvest and counted in the absence of scintillation fluid on a β-plate reader (Packard Instrument Co.). Three individual wells were analyzed per data point.
As an indication of T cell responses in vivo, mice were examined for evidence of GVHD by clinical characteristics (weight loss and appearance) and tissue histopathology using a semiquantitative histopathological scoring system as described previously (48).
IgG and IgM serum levels.
Ig levels were determined on serial dilutions of sera by ELISA at the University of Minnesota Cytokine Reference Laboratory as described previously (48).
Engraftment in organs.
Transplanted animals were anesthetized and perfused intracardially with 10 ml of 10 mM EDTA/1× PBS, followed by 10 ml Z-Fix (Anatech). Blood was collected before perfusion with PBS and BM between perfusion with PBS and Z-Fix. After systemic perfusion with PBS and Z-Fix, nonhematopoietic organs were removed and post-fixed in Z-Fix for 24 h at 4°C. Fixed tissues were washed with 1× PBS, cryoprotected by overnight incubation in 30% sucrose, quick-frozen in optimum cutting temperature compound, and stored at −80°C. 6-μm cryosections were thaw-mounted onto glass slides and fixed in acetone for 5 min. Spleen, LNs, and thymus were immunostained for donor- derived lymphocytes using anti–CD3-PE, anti–CD4-biotin, rabbit anti–GFP, anti–CD19-PE, anti–CD11b-PE, anti–CD11c-biotin, and anti–CD45.2-biotin (all from BD Biosciences). Biotinylated antibodies were detected with streptavidin-Cy5 (BD Biosciences), and rabbit antibodies were detected with anti–rabbit Alexa 488 (Invitrogen). Stained tissues were analyzed using a confocal microscope (FV500; Olympus) and Fluoview software (version 3.2; Olympus).
Online supplemental material.
The online supplemental material contains a more extensive description of the cells transplanted (including phenotype, Oct3a transcript and protein level, and cytogenetics) and the level of engraftment in each individual animal. Additional information is available regarding multilineage reconstitution in the blood, BM, and spleen.
We thank M. Blackstadt for help with quantitative RT-PCR; A. Breyers and L. Lien for help with MAPC culture; P. Marker for cell sorting; A. Price and M. Riddle in the B.R. Blazar lab for technical assistance; L. Jerabek for excellent laboratory management; and D. Bhattacharya and T. Serwold of the I.L. Weissman laboratory for helpful advice and assistance.
The work was supported by DK5829, HL71228, and HL076653 to C.M. Verfaillie; HL52952, HL49997, HL63452, HL073794, and P01 AI 056299 to B.R. Blazar; and HL058770 and AI047457 to I.L. Weissman. S.J. Dylla was supported by an American Cancer Society Edward-Albert Bielfelt Postdoctoral Fellowship (PF-04-087-01-LIB). S. Frommer was supported by National Institutes of Health (NIH) Muscle Training Grant and NIH Musculoskeletal Training Grant (T32AR07612), B. Pelacho was supported by AHA0525748Z, and Y. Heremans was supported by a postdoctoral fellowship from the Juvenile Diabetes Research Foundation.
C.M. Verfaillie has received research funding from Athersys Inc. for work with MAPCs unrelated to the studies in this manuscript. No other authors have conflicting financial interests.
Abbreviations used: eGFP, enhanced GFP; ESC, embryonic stem cell; GVHD, graft-versus-host disease; HSC, hematopoietic stem cell; LT-HSC, long-term repopulating HSC; MAPC, multipotent adult progenitor cell; mESC, mouse ESC; NOD, nonobese diabetic; PB, peripheral blood.
M. Serafini and S.J. Dylla contributed equally to this work.