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Recent studies with Helicobacter-infected mice have shown that bone marrow-derived cells can repopulate the gastric epithelium and progress to cancer. However, it has not been established which cellular subset can potentially contribute to the epithelium. The aim of this study was to investigate the ability of bone marrow-derived mesenchymal stem cells (MSCs) that express cytokeratin 19 (K19) to contribute to the gastric epithelium. MSCs cultures were established from whole bone marrow and expression of K19 was detected in a minority (1 of 13) of clones by real-time PCR and immunostaining. Transfection of a K19-green fluorescent protein (GFP) vector and isolation of GFP-expressing colonies generated high K19-expressing MSC clones (K19GFPMSC). Incubation of MSCs with gastric tissue extract markedly induced mRNA expression of gastric phenotypic markers and was observed to a greater extent in K19GFPMSCs compared with parental MSCs and mock transfectants. Both K19GFPMSCs and GFP-labeled control MSCs gave rise to gastric epithelial cells after injection into the murine stomach. In addition, after blastocyst injections, K19GFPMSCs gave rise to GFP-positive gastric epithelial cells in all 13 pups, whereas only 3 of 10 offspring showed GFP-positive gastric epithelial cells after injection of GFP-labeled control MSCs. Although K19 expression could not be detected in murine whole bone marrow, H. felis infection increased K19-expressing MSCs in the circulation. Taken together, our results show that bone marrow-derived MSCs can contribute to the gastric epithelium. The K19-positive MSC fraction that is induced by chronic H. felis infection appears to be the important subset in this process.
There is considerable evidence that bone marrow-derived cells (BMDCs) show plasticity. Studies in gender-mismatched human bone marrow transplant recipients have provided evidence that BMDCs contribute to the epithelium of the liver,1 lung,2,3 and gastrointestinal tract.4–8 Furthermore, bone marrow transplant experiments in mice have shown that engraftment of BMDCs in epithelial tissues supports maintenance of the epithelium and aids in tissue healing.2,9–13 Work from our laboratory provided the first clear evidence of the contribution of BMDCs to the development of cancer. In mice reconstituted with labeled bone marrow, chronic Helicobacter felis (H. felis) infection induced repopulation of the gastric epithelium with BMDCs and progression of these cells to intraepithelial cancer.14 BMDCs have also been detected in human epithelial neoplasias such as renal cell carcinoma,15 colon adenoma,16 and lung cancer16,17 in patients who have undergone a previous bone marrow transplant.
In the majority of bone marrow transplant studies in mice and humans, whole bone marrow cells or the enriched hematopoietic stem cell fraction were used to reconstitute the recipients' bone marrow. However, in most cases, the infused donor cells were heterogeneous and it remains uncertain which cellular subset within the graft actually contributed to the epithelial lineage.8,18 In our previous study, the mesenchymal stem cell (MSC) fraction of bone marrow was proposed to be a possible source of engrafted BMDCs because induction of gastric epithelial phenotype markers after treatment with gastric tissue extract was detected in this fraction, but not in the HSC fraction.14 Nevertheless, direct evidence that MSCs contribute to the gastric epithelium has not been established.
MSCs constitute only a small fraction of the bone marrow19,20 and originally were characterized as colony-forming fibroblast-like cells19,21,22 that adhered to plastic in culture and possess the ability to differentiate into osteocytes, chondrocytes, adipocytes.20,23 Studies in humans and animals have also reported the in vitro differentiation of MSCs into endodermal, ectodermal, and mesodermal tissues, such as pneumocytes24 and hepatocytes,25 neural cells,26 and cardiomyocytes,27 respectively. More recently, the pluripotency of MSCs has been shown in vivo.28–30
In addition to their potential for differentiation into both mesodermal and endodermal lineage, some multipotent MSC subsets have been shown to express endoderm-associated genes such as cytokeratins and Sox 17.29,31,32 Cytokeratins are a family of intermediate filaments that are expressed in epithelial cells and appear to be critical for the maintenance of the cytoskeleton.33 Among the various cytokeratins, keratin 19 (K19) has been reported to be expressed in the progenitor zone of the epidermis34 and the proliferative zone of the gastrointestinal tract,35–38 and is thought to be an early marker of epithelial cell lineage.39 Transgenic studies in mice have shown that K19 is expressed in the neck/isthmus region of the gastric glandular unit, the area where epithelial progenitors and committed precursor cells are believed to reside.35 Importantly, BMDCs have been shown to consistently express K19 upon recruitment and engraftment in the stomachs of H. felis-infected mice.14
In this study, we assessed the ability of bone marrow-derived MSCs to differentiate toward a gastric epithelial cell lineage. We addressed the hypothesis that K19 expression could be used to identify a subset of MSCs that possess the ability to contribute to gastric epithelial cells. Our results suggest that K19-expressing MSCs are absent from the normal bone marrow but are induced by culture conditions in vitro, and in response to H. felis infection in vivo. Thus, K19-expressing MSCs possess plasticity along a gastric epithelial lineage and may potentially have a role in healing and repair of the gastric epithelium.
All mice studies and breeding were carried out under the approval of IACUC of Columbia University. Ninety-eight mice were used in this study; 75 of them, including C57BL/6 wild type (WT) mice (8–10 weeks old) and chicken β-actin-enhanced green fluorescent protein (EGFP) transgenic mice (8–10 weeks old), were purchased from Jackson Laboratories (Bar Harbor, ME, USA). Twenty-three study mice were chimeric mice derived from blastocyst injection (Supplementary Table 1).
Bone marrow cells were collected by flushing femurs and tibias with Hank's balanced salt solution (HBSS) and plated at a density of 106 cells/cm2 in murine mesenchymal medium with murine mesenchymal supplements (MesenCult, Stem Cell Technologies, Vancouver, BC, Canada). MSC cultures were derived from five WT mice and five chicken β-actin EGFP transgenic mice, and maintained individually. Non-adherent cells were removed after 24 h, and culture media were replaced every 5 days. The cells became confluent within 2–3 weeks at 37°C in humid air containing 5% CO2. Adherent cells were detached by 0.25% trypsin and 0.02% ethylene diaminetetraacetic acid (EDTA) at 37°C for 2 min and subsequently passaged in the ratio of 1:3 to achieve the required number. The cells of fifth to tenth passage were used for the following protocols.
MSCs were plated at a density of 5 × 105 cells per cm2 and maintained as described above. At day 14, the medium was removed from the wells, washed twice with phosphate-buffered saline (PBS) and fixed/stained with 3% Crystal violet in 100% methanol for 10 min at room temperature. Cells were washed with PBS and colonies were then counted.
To induce adipocyte differentiation, the subconfluent cells were cultured with MesenCult Stem Cell Medium containing 5.0 μg/ml insulin, 50 μM indomethacin, 1 μM dexamethasone and 0.5 μM 3-Isobutyl-1-methylxanthine. After 14 days, these cells were fixed with 4% paraformaldehyde for 15 min, and stained with Oil Red-O.
To induce osteocyte differentiation, the subconfluent cells were cultured with MesenCult Stem Cell Medium containing 1 nM dexamethasone, 20 mM β-glycerolphosphate, 50 μM l-ascorbic acid 2-phosphate sesquimagnesium salt, and 50 ng/ml l-thyroxine sodium pentahydrate. After 14 days, these cells were fixed with 4% paraformaldehyde for 15 min, and characterization was performed by Alizarin Red staining, which detects calcium deposition.
A total of five stomachs from WT mice (three male and two female mice), aged 8–12 weeks, were used for gastric tissue extract. For each experiment, gastric tissue extract from one stomach was used. The paste from one stomach, made by mortar and pestle, was mixed with 10 ml of MesenCult Stem Cell Medium and incubated at 4°C for 24 h. The mixture was centrifuged at 6000 r.p.m. for 20 min, and the supernatant was obtained and filtered using a 0.2 μm membrane filter. MSCs were cultured with medium containing gastric extract for 5 days at 37 °C in humid air containing 5% CO2. Phenotype markers were detected by real time-PCR (RT-PCR); all primer sequences can be found in Supplementary Table 2.
cDNAs encoding the mouse K19 promoter sequence and EGFP gene were cloned by PCR from K19-β Gal vector (Brembeck FH 2001) and pEGFP N1 vector (Clontech, Mountain View, CA, USA), respectively. They were subcloned into a pcDNA3.1 plasmid (Invitrogen) in which a neomycin selectable marker was encoded. After sequencing, the DNA plasmids were transfected into MSCs with lipofectamine 2000 (Invitrogen) according to a standard protocol (Lipofectamine 10 μl per vector DNA 4 μg). Then cells were cultured with MesenCult Stem Cell Medium containing 150 mg/ml of G418. Colonies were chosen 7 days after transfection and then cultured. GFP+ clones were selected under fluorescence microscopy and the expression of GFP was confirmed by flow cytometry. We used the subclones within five passages after establishment for all experiments and confirmed the expression of GFP and K19 in every passage by flow cytometry and RT-PCR, respectively.
Subconfluent MSCs were removed from the culture plates by treatment with 0.25% trypsin/EDTA solution and the cells were then treated with MesenCult Stem Cell Medium to stop the reaction. The cells were washed once with PBS and a cell suspension (10 000 000 cells per 1 ml PBS) was prepared. Four-week-old WT mice were anesthetized with inhalation of isoflurane, the center of the upper abdomen was opened by a 1 cm incision, and the stomach was lifted outside the abdomen. About 10 μl of the cell suspension was injected into each of several points of gastric wall by using a fine glass needle. The abdominal wall was closed by a 5–0 polypropylene surgical suture. Gastric tissue sections were prepared from mice at 2 weeks after injection to detect GFP-positive cells.
Blastocyst injections were performed in the Transgenic Core Facility of Columbia University Medical School. Three and half day-old blastocysts were extracted from the uteri of WT pregnant females, injected with 10–15 GFP-labeled MSCs and implanted in uteri of Swiss Webster pseudopregnant females. Pups were euthanized at 8 weeks of age and histological or PCR analyses were conducted on stomachs and other organs to detect GFP-labeled cells.
Bone marrow transplantation and H. felis infection were carried out as previously described.17 Briefly, 35 WT female recipient mice received lethal irradiation (950 cGy) from a Cs137 source and after 3 hours, donor whole bone marrow cells (5 million cells in 200 μl) were infused via the tail vein. Whole bone marrow cells were prepared from chicken β-actin EGFP transgenic donor mice, as described above. Five of the recipients did not receive donor bone marrow cell infusion and served as additional controls. Fifteen of the study mice (aged 3 months) received inoculation of H. felis by oral gavage, whereas the other 15 recipients remained uninfected. H. felis (ATCC 49179) was used for oral inoculation as described previously.14 The organism was grown for 48 h at 37°C under microaerobic conditions on 5% lysed horse blood agar. Bacteria were harvested and inoculated (at a titer of 1010 organisms per ml) into brain heart infusion broth with 30% glycerol added. The bacterial suspension was frozen at −70°C. Before use, aliquots were thawed, analyzed for motility, and cultured for evidence of aerobic or anaerobic bacterial contamination. The inocula (0.5 ml) were delivered by gastric intubation into each test mouse three times at 2-day intervals using a sterile oral catheter.59 After 1 year of infection, mice were euthanized and both bone marrow and peripheral blood were extracted and used for MSC culture and mRNA detection.
We established MSC cultures from whole bone marrow of mice based on their ability to adhere to plastic tissue culture dishes, as previously described.19–23 Non-adherent cells were removed, and the primary cultured MSCs became confluent within 2–3 weeks. They grew exponentially for more than 15 passages without signs of senescence or differentiation. After five passages, the pooled MSCs displayed the abilities of colony formation (Figure 1a) and differentiation into both adipocyte and osteocyte lineages under previously defined conditions (Figure 1b). Flow cytometric analysis of these primary MSC cultures revealed that the majority of the cells expressed Sca1 (94.4%), but not CD45, c-kit, or Flk1 (Figure 1c).
As recent reports have suggested that a subpopulation of cultured MSCs exhibit multipotency in association with expression of embryonic stem cell markers,29,30 we examined the expression of Nanog and Oct-3/4. Low levels of Nanog, but not Oct 3/4, expression were detected in our cultured MSCs (Supplementary Figure S1). Following treatment with gastric tissue extracts (see Materials and Methods), the cultured MSCs altered their morphology from spindle-like fibroblastic to oblong or irregular appearance under phase contrast microscopy (Figure 1d). In addition, treatment of MSCs with gastric extract resulted in increased expression of gastric epithelial phenotypic markers, such as K19, TFF2, MUC5AC, MUC6, H/K-ATPase, and chromogranin A (Figure 1e). These markers represent distinct epithelial cell lineages in the gastric glands (Supplementary Figure S2), suggesting that MSCs may be able to differentiate into any or all lineages. There was no difference in the induction of gastric phenotypic markers using gastric tissue extract prepared from male or female mice (data not shown).
We found that K19 was expressed at a low level in most cultured MSCs although a small number of MSCs from select colonies retained high expression, as confirmed by immunocytochemical staining (Figure 2a). Individual MSC colonies were isolated from primary cultures, expanded, and then tested for K19 expression by RT-PCR. High levels of K19 mRNA expression could be detected in approximately one out of 13 subclones derived from a single mouse (Figure 2b). This implied that although K19 expression was present and detectable in a small subset of MSCs, K19+ cells could clonally expand and be enriched for K19 expression. Most of these subclones, including the clone with the highest K19 expression, retained the ability to differentiate into osteoblast and adipocyte lineages under appropriate culture conditions (Figure 2c).
To isolate the small number of MSC clones that express K19, primary cultured MSCs were transfected with a K19–EGFP expression vector and stable clones were selected following G418 treatment. Fluorescence microscopy revealed that 3 of 11 isolated clones from the same parent MSCs were positive for GFP expression (Figure 3a) and these clones (K19GFPMSC) were designated K19GFPMSC no. 3, no. 4, and no. 5. Flow cytometry revealed that the percentage of GFP-positive cells was 10.0, 96.2, and 78.6% for K19GFPMSC no. 3, no. 4, and no. 5, respectively (Figure 3b). Real-time PCR analysis revealed 40- and 35-fold increases in K19 mRNA expression in K19GFPMSC no. 4 and no. 5, respectively, compared with the parent MSCs (Figure 3c). The average K19 mRNA expression of K19GFPMSC no. 3 was increased approximately 42-fold (Figure 3c) when compared with the parental MSCs, and the average K19 expression in clone no. 3 did not show a statistical difference from the other two clones despite the lower percentage of GFP+ cells. K19 mRNA expression in K19GFPMSC no. 3 was primarily due to the high level of K19 expression in the GFP+ fraction, with the GFP+ cells having a 66-fold increase in expression compared with 16-fold for the GFP− cells (Figure 4d). Expression of K19 protein in the three stable MSC clones was confirmed by immunofluorescent staining (Figure 3d). Flow cytometric analysis revealed that expression of a variety of cell surface markers (including Sca-1, CD45, c-kit, Flk1, and F4/80) in the K19GFPMSC clones were roughly similar to that in the parent MSCs (Figure 3b, see also Figure 1c). Although all three K19GFPMSC clones did not express Oct3/4 (Supplementary Figure S1), they did express Nanog and retained the ability to differentiate into adipocyte and osteocyte lineages in culture (Figure 3e).
Similar to what had been observed in the parental MSCs, after 5 days of treatment with gastric tissue extract, K19GFPMSCs altered their morphology from spindle-like to oblong or irregular shape (Figure 4a). In addition, the K19GFPMSC clones had significant increases in mRNA expression of gastric phenotypic markers, with up to 60-, 300-, and 170-fold increases in K19GFPMSC clones no. 3, no. 4, and no. 5, respectively. In contrast, less than 10-fold increases were observed in the parental MSCs and mock transfectants (Figure 4b). Although the induced gastric phenotype mRNA expression in K19GFPMSCs treated with gastric tissue extract was much lower than that seen in gastric tissues, this observation was reproducible in at least three separate experiments (Supplementary Figure S3). In contrast, stimulation of MSCs with colonic or pancreatic tissue extract did not induce expression of gastric phenotype markers, although the treatments modestly increased expression of genes associated with their respective tissues (Supplementary Figure S4c).
After twenty-eight days of culture, sorted GFP+ cells from K19GFPMSC no. 3 gave rise to both GFP+ and GFP− cells, whereas GFP− cells never gave rise to GFP+ cells under the same conditions (Figure 4c). BrdU assays showed that GFP+ cells exhibit higher proliferation rates than GFP− MSCs (eight samples each, unpaired Student's t-test P = 0.0029) (Figure 4f). RT-PCR revealed a higher basal level of K19 mRNA expression in GFP+ MSCs compared with GFP− MSCs (Figure 4d). Following treatment with gastric tissue extract, the K19-expressing GFP+ fraction showed greater upregulation of gastric phenotypic markers, such as TFF2 and H/K-ATPase, compared with the GFP− fraction (Figure 4e). Single cell sorting (Figure 4g) revealed that K19GFP no. 3 cells could divide and generate colonies (Figure 4h). Fourteen days after plating, there were 5.3 ± 2.5 and 13.6 ± 3.5 colonies (P = 0.029) from GFP− and GFP+ cell fractions, respectively (n = 3). After treatment with gastric tissue extract, the overall pattern of gastric phenotype marker expression was similar between colonies from the single-sorted and pooled GFP+ and GFP− MSCs (Figure 4i). Accordingly, the difference between GFP+ and GFP− MSCs remained significant in the analysis of colonies from single sorted clones. In addition, isolation of single colonies from GFP+ MSCs treated with gastric extract exhibited the same pattern of gene expression when re-incubated with gastric extract (data not shown). Taken together, these data show that 10% of K19GFPMSC no. 3 were GFP+ and expressed the highest K19 levels and had a greater potential to upregulate certain gastric phenotypic markers without specifying a particular differentiated gastric epithelial lineage. The results suggest that the MSCs with higher K19 expression may represent a progenitor cell fraction.
To test the differentiation ability of MSCs in adult animals, two hundred thousand (200 000) cells from either K19GFPMSC no. 4 or control MSCs obtained from the bone marrow of chicken β-actin EGFP transgenic mice (GFPMSC), were injected directly into the stomach wall of WT-mice (Supplementary Figure S5, see also Figure 1c). Twenty-four hours after injection of control GFPMSC cells, GFP+ cells were distributed in the mucosa, submucosa, and subserosa of the stomach (Supplementary Figure S6). A similar pattern was observed for the K19GFPMSC cells. Two weeks after injection of K19GFPMSC no. 4, GFP+ cells could be detected scattered throughout the gastric epithelium, with many showing expression of the epithelial-specific marker, E-cadherin (Figure 5a). Stomach sections from mice injected 2 weeks earlier with the control GFPMSCs had fewer total GFP cells, but some were also positive for E-cadherin in the gastric epithelium (Figure 5b).
In females receiving an injection of male MSCs, we performed Y chromosome FISH to detect any MSC-derived cells that did not express GFP due to silenced chicken β-actin/k19 promoter activity. However, we found a similar number of Y chromosome-positive cells scattered throughout the epithelium, suggesting that this procedure offered little advantage over GFP detection (data not shown). We also injected K19GFPMSC no. 4 and GFPMSC into gastric walls of WT mice with long-term (12 months) H. felis infection to investigate whether a chronic inflammatory environment wound enhances the engraftment of MSC. However, there was no significant increase in the number of engrafted GFP-positive cells in the gastric epithelium (data not shown).
To test the differentiation ability of these cells under embryonic conditions, we performed blastocyst injections of GFP-labeled MSCs. Following blastocyst injection of control GFPMSCs, the GFP DNA sequence was detected by PCR in tail DNA from 6 of 10 chimeric offspring (Supplementary Figure S7A), and analysis of gastric sections from 8-week-old mice showed GFP+ cells in the gastric epithelium in 3 of 10 animals (Supplementary Figure S7B). Some of the GFP+ gastric cells also stained E-cadherin positive (Figure 5c). In comparison, GFP+ cells could be detected in the gastric epithelium of all 13 pups derived from blastocyst injections of K19GFPMSC no. 4, (Supplementary Figure S7C and S7D) with many GFP+ E-cadherin+ cells distributed throughout the gastric epithelium (Figure 5d). We confirmed the localization of GFP inside and E-cadherin on the membrane of the same cells under confocal microscopy (Supplementary Figure S8). Anti-GFP immunohistochemistry further confirmed engraftment of injected MSCs into the gastric mucosa (Figure 5e). To track the differentiation of these engrafted MSCs, we performed immunohistochemistry for H/K-ATPase, intrinsic factor, chromogranin A, MUC5AC and MUC6, although we did not find any GFP+ cells coexpressing these markers in any of the sections (Figure 5f). The GFP detection rate, based on the number of animals positive for GFP expression and the number of GFP+ cells per high-power field (HPF) (average of 10 HPFs), from both the gastric wall injection study and the blastocyst injection study, are summarized in Figure 5g. Overall, it appeared that K19GFPMSCs had an engraftment rate equal to or greater than that of pooled GFPMSCs. We performed flow-cytometric analysis of bone marrow from chimera mice derived from blastocyst injections, and found a very small number of GFP+ cells in only a few mice. Gastric epithelial engraftment was seen in mice both with and without bone marrow engraftment, indicating that blastocyst-injected MSC's were capable of primarily engrafting into the foregut endoderm, rather than engrafting into the adult gastric epithelium following initial engraftment in the bone marrow. GFP+ cells were also detected in stromal areas of the epidermis of these mice (Supplementary Figure S9), indicating that K19GFPMSCs retain the capacity to contribute to stromal lineages.
We did not detect expression of K19 mRNA by RT-PCR in fresh bone marrow cells from mice, regardless of whether they had chronic H. felis infection (not shown). However, K19 mRNA expression was detected in the mononuclear cell fraction of peripheral blood of mice and was highly upregulated by chronic H. felis infection (Figure 6a). Because there are currently no consensus markers to directly isolate MSCs from peripheral blood, the mononuclear cell fraction of peripheral blood from mice with H. felis infection was seeded onto plastic plates with MSC culture medium. Spindle-like fibroblastic cells proliferated exponentially whereas many round-shaped cells did not grow and were lost from the culture after passage (Figure 6b). We designated the spindle-like fibroblastic cells as peripheral blood-derived MSCs (PBMSCs) because they showed adipocyte and osteoblast differentiation under appropriate culture conditions (Figure 6c). PBMSCs were established from 5 of 13 mice (38.5%) that were chronically H. felis-infected and from only 1 of 14 (7.1%) age-matched uninfected control mice. Most of the PBMSCs were GFP+ when they were established from mice that received bone marrow transplants from chicken β-actin EGFP donor mice (Figure 6d), suggesting the bone marrow origin of these PBMSCs. In addition, PBMSCs had increased expression of the gastric epithelial phenotypic markers, TFF2 and H/K-ATPase, after treatment with gastric tissue extract in vitro (Figure 6e), showing a similarity in phenotype with bone marrow-derived cultured MSCs. However, there was no significant difference in the expression of K19 or other markers that were tested.
A number of studies have shown that mesenchymal stem cells possess unexpected plasticity and are able to differentiate across germ layer boundaries to give rise to epithelial tissues.28–30 Previous reports by our group suggested MSCs as a possible candidate for the bone marrow-derived progenitor cells that give rise to cytokeratin-positive metaplastic cells in the gastric epithelium during chronic H. felis infection.17 In vitro studies indicated that MSCs, but not HSCs, could acquire an epithelial morphology and upregulate the expression of epithelial markers such as cytokeratin 19, when exposed to gastric extract.17 In this study, we show that the K19-expressing MSC subclones possess all of the gastric differentiating abilities of MSCs, and can give rise to gastric epithelial cells when injected into the adult mouse stomach or early blastocysts. Finally, K19-expressing MSCs give rise to K19− MSCs, and are mobilized into the circulation by chronic H. felis infection.
Bone marrow-derived MSCs have been isolated and characterized in the past based on their fibroblast-like morphology, ability to proliferate in vitro, and potential to differentiate into multiple lineages.40–45 Nevertheless, no clear consensus regarding the expression of specific cell surface markers has emerged.40–42,46 To isolate MSCs in our studies, we cultured whole bone marrow on plastic tissue culture plates with medium containing 10% serum and passaged the adherent cells more than five times to eliminate contamination by hematopoietic and endothelial fractions. We showed that our MSCs were CD45−, Flk1−, F4/80− by flow cytometry. We confirmed their MSC phenotype by their ability to form colonies in soft agar and differentiation to osteocytes and adipocytes. However, even cultured and enriched MSCs remained morphologically heterogeneous,46 and colonies derived from them were diverse in both appearance and differentiation potential.40,46–48
Cytokeratin 19 is a marker of early epithelial progenitors,39 particularly in the stomach35–38 and we noted upregulation of K19 when pooled MSCs were exposed to gastric tissue extract. We investigated K19 expression in individual MSC subclones and found that only a minority of individual clones spontaneously expressed K19 under basal culture conditions. Using a K19–GFP transfection approach, we selected K19-expressing clones and showed that they were generally equivalent to the parental MSCs in terms of their capacity to differentiate into gastric epithelial cells when injected into adult mouse stomachs or early blastocysts. In addition, K19–GFP+ cells gave rise to GFP− cells that possessed limited potential of in vitro differentiation. This indicated that the K19+ cells are the more primitive fraction in the cell line.
Although the K19–GFPMSCs appeared to possess some degree of longevity and self-renewal ability, in vivo studies with these passaged cells raise some question as to whether these cells are progenitors rather than true stem cells. In all of the stomach sections in which GFP positivity was detected, positive cells presented as single cells scattering throughout the gastric epithelium. Neither GFP+ clonal glands nor GFP+ clusters were detected. This is consistent with previous reports that bone marrow-derived cells are detected as single differentiated epithelial cells in the uninjured gastrointestinal tract.8,10,30 In addition, none of the single, scattered GFP+ cells showed expression of H/K-ATPase, indicating limited ability to differentiate into parietal cells, the most abundant type of differentiated cells in the gastric epithelium. These GFP+ gastric epithelial cells also did not express other markers of differentiated gastric epithelial cells, such as intrinsic factor, chromogranin A, MUC5AC or MUC6. A possible explanation for the lack of clonal glands is that MSCs do not engraft into the stem cell niche under normal conditions. However, it is also likely that our MSCs gradually lost their stemness or multipotentiality during culture. Our in vitro studies indicate that even after exposure to gastric extract, they induce expression of multiple gastric genes rather than a single, lineage-defining gene, consistent with a progenitor phenotype. Multipotent mesenchymal stem cells have been reported to exist in the bone marrow,29,30,32,49,50 and these cells show expression of ES cell marker genes, such as Oct3/4 and Nanog.29,30 In this study, both the parental MSC cultures and the K19+ MSC clones expressed Nanog, but were negative for Oct3/4 and SSEA-1. This suggests that they are not identical with the previously reported multipotent mesenchymal progenitor cells. Finally, it is possible that the injected MSCs undergo cell fusion in vivo, and this could explain the finding of single-scattered GFP+ cells in the stomach.51
Although K19 mRNA expression was not detectable in the freshly isolated bone marrow mononuclear cell fraction, it was detected in the peripheral blood of mice with chronic H. felis infection. Studies examining K19 expression in both cultured bone marrow- and peripheral circulation-derived MSCs suggest that removal of MSCs from their normal bone marrow niche may in part trigger the upregulation of K19 and the epithelial progenitor program. Furthermore, we were able to grow more MSC cultures from peripheral blood of H. felis-infected mice than that from uninfected control mice. Donor-derived MSCs were identified in the peripheral blood of mice having undergone both bone marrow transplantation and chronic infection with H. felis. The presence of MSCs in the peripheral blood,52–54 and mobilization of these bone marrow-derived cells into the peripheral circulation under chronic inflammatory states or injury has previously been described.55,56 Given that no definitive cell surface markers are currently available to distinguish MSCs from non-MSC cells in mice, we could not completely exclude the possibility that the detected K19-expressing transcripts in peripheral blood are due to phagocytosed cell fragments liberated from the injured gastric epithelium. Nevertheless, taken together, our results suggest that the expression of K19 is induced in bone marrow-derived MSCs after they are recruited into the circulation in response to chronic H. felis infection.
Our in vitro study with gastric tissue extracts suggests that K19 expression is induced in MSCs when they are recruited into the gastric tissue environment. However, our finding of K19-expressing MSCs in the peripheral circulation also suggests the possibility that MSCs express K19 upon release from the bone marrow niche and/or after exposure to factors in the blood. These cells may represent epithelial progenitor cells uncommitted to a specific epithelial lineage, possibly induced by systemic factors released from inflamed gastric mucosa, whereas exposure to the gastric environment reinforces K19 expression and represents cells committed to the gastric epithelial lineage. Identification of MSC-specific markers would be necessary to isolate these cells from peripheral blood and determine more precisely their in vivo biology.
We treated cultured MSCs with whole gastric tissue extract based on earlier studies.14 There are several possible morphogenetic signals that have been reported to participate in the morphogenesis of gastrointestinal tract, including extracellular matrix interactions,57 sonic hedgehog,58 transforming growth factor (TGF) β,59 fibroblast growth factors (FGFs),60 epimorphin,61 hepatocyte growth factor (HGF),62 and bone morphogenetic proteins.63 Despite this work, no definitive combination of factors has been shown to successfully induce gastric differentiation in MSCs in vitro. Further investigation of specific components in the gastric extracts used in this study may provide important insights regarding gastric differentiation.
In this study, we found that chicken β-actin eGFP MSCs (hemizygous, C57BL/6-Tg (ACTB–EGFP) 10sb/J, JAX Stock number: 003291) expressed weak, primarily nuclear GFP when engrafted as epithelial cells, whereas the GFP in the epithelial cells derived from K19GFPMSC was quite robust. Chicken β-actin eGFP was previously reported to be poorly expressed in the gastrointestinal tract,64,65 and can traffic back into the nucleus following expression in the cytosol.66 Nevertheless, epithelial expression of GFP was supported by the observation that GFP and E-cadherin were co-localized under confocal microscopy (Supplementary Figure S7C-S7E).
In conclusion, we report that bone marrow-derived MSCs can contribute to the gastric epithelium in vivo, and that the K19+ MSC subset is most likely responsible for this process. We also report K19+ MSC mobilize to the peripheral blood in the setting of chronic H. felis infection. Although further studies are necessary to determine whether these MSCs can contribute to carcinogenesis, our data provides support for an MSC subset that could potentially contribute to gastric epithelial regeneration and repair.
We thank Dr Victor Lin of the Transgenic Core Facility of Columbia University Medical School for blastocyst injection, Ms. Kelly S. Betz, Dr Melitta Penz, and Ms. Shanisha Gordon for animal care and technical assistances. This work was supported by grants from NIH 5R01 CA120979-02 (TCW), NIH R01 DK060694 (AKR) and The Uehara Memorial Foundation (TO).