Immunosuppressive and Hematopoiesis-Supporting Properties of Stromal Cells at Low Oxygen

Elena R Andreeva, Irina V Andrianova, Polina I Bobyleva, Ludmila B Buravkova

  Open Access OPEN ACCESS  Peer Reviewed PEER-REVIEWED

Immunosuppressive and Hematopoiesis-Supporting Properties of Stromal Cells at Low Oxygen

Elena R Andreeva1,, Irina V Andrianova1, Polina I Bobyleva1, Ludmila B Buravkova1

1Cell Physiology lab, Institute of BioMedical Problems, Russian Academy of Sciences, Moscow, Russia

Abstract

In adults, low differentiated stromal cells like fibroblasts, multipotent mesenchymal stromal cells, reticular cells etc. are important integrative components of tissue homeostasis and regeneration. The purpose of this study was to compare immunomodulatory activity and hematopoiesis-supportive capacity of two human stromal cell types: fetal fibroblasts (fFBs) and multipotent mesenchymal stromal cells (MMSCs) under different oxygen tension (20% vs. 5%). Surface immunophenotyping by flow cytometry revealed that MMSCs and fFBs were СD90, СD105, HLA-ABC positive and СD34, СD45, HLA-DR negative regardless of the О2 concentration. The percentage of T-cells was relatively unchanged after 72 hours co-culture with stromal cells; the proportion of B- and NK-cells was increased, but the share of CD3+/HLA-DR+ cells was decreased when co-culturing with both MMSCs and fFBs. This reduction was statistically significant at 5% O2 in comparison with 20% O2 (p < 0.05). CD3+/CD25+ cells decreased after co-culture with both stromal cells in 20% O2. This effect was revealed only for MMSC at 5% O2. After 72 hours in co-culture with MMSCs, mononuclear cells from umbilical cord blood (CBMCs) maintained the same number of colony forming units (CFU) as compared with the initial CBMC suspension. The number of CFU was 30% higher at 5% O2 than in 20% O2 (p < 0.05). The CFU number in CBMCs after co-culture with fFBs decreased and a stimulatory effect of low oxygen was not observed. CBMCs that were adhered to MMSCs formed colonies of undifferentiated progenitors after 2 weeks of co-culture both at 20% and 5% O2. Colonies were not found on fFBs. The immunomodulatory potency and the hematopoiesis-supportive capacity of stromal cells can vary depending on their tissue origin and may be modified by the partial pressure of oxygen.

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Cite this article:

  • Andreeva, Elena R, et al. "Immunosuppressive and Hematopoiesis-Supporting Properties of Stromal Cells at Low Oxygen." American Journal of Biomedical Research 1.1 (2013): 7-12.
  • Andreeva, E. R. , Andrianova, I. V. , Bobyleva, P. I. , & Buravkova, L. B. (2013). Immunosuppressive and Hematopoiesis-Supporting Properties of Stromal Cells at Low Oxygen. American Journal of Biomedical Research, 1(1), 7-12.
  • Andreeva, Elena R, Irina V Andrianova, Polina I Bobyleva, and Ludmila B Buravkova. "Immunosuppressive and Hematopoiesis-Supporting Properties of Stromal Cells at Low Oxygen." American Journal of Biomedical Research 1, no. 1 (2013): 7-12.

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1. Introduction

Stromal cells of mesenchymal origin such as fibroblasts (FBs) and multipotent mesenchymal stromal cells (MMSCs) play an important role of the physiological and regenerative microenvironment modifying certain properties of other cell types. MMSCs have generated a great deal of excitement and promise as a potential source of cells for cell-based therapeutic strategies due to their immunosuppressive properties and immunotolerance [1, 2, 3]. Recent studies have demonstrated that FBs can be functionally equivalent to MMSCs to some extent [4, 5]. In addition, stromal cells constitute the basic structural and functional component of the highly specialized hematopoietic tissue niche where the cell-cell interaction is controlled by microenvironment factors, with partial pressure of oxygen being the leading one. Up to now, a large amount of data has been gathered on how changes in О2 levels modulate cell properties, with regard to MMSCs in particular [6, 7]), which may affect their relationship with other cells. In the present paper we have analyzed the immunomodulating and hematopoiesis-supporting properties of two types of stromal cells: human MMSCs from adipose tissue and human fetal FBs. In addition, the effects of oxygen level on the interaction of human stromal cells and differentiated human MMSCs from adipose tissue and human fetal FBs is also investigated. Besides, the effects of oxygen level on the interaction of human stromal cells and differentiated and progenitor blood mononuclear cells was studied in vitro.

2. Materials and Methods

2.1. Cell Culture

Multipotent mesenchymal stromal cells (MMSCs) were isolated from the stromal-vascular fraction of human adipose tissue as previously described [8] with some modifications [7]. Briefly, adipose tissue was obtained from elective liposuction procedures under local anesthesia from healthy patients after informed consent was obtained in the multidisciplinary clinic “Souz” (Moscow, Russia) and treated with 0.075% collagenase IA (Sigma-Aldrich, USA). After washing, cells were resuspended in DMEM low glucose (MP Biomedicals, USA), supplemented with 10% FBS (Hyclone, USA), 250μg/ml amphotericin, 5μg/ml streptomycin, 5U/ml penicillin, and 2mM glutamine (MP Biomedicals, USA).

Human fetal fibroblasts (fFBs) were kindly gifted by Prof. B.K.Gavriluk (Institute of Theoretic and Experimental Biophysics, Pushchino, Russia). Cells of 2-8 passages were cultured in the same culture medium and gaseous conditions as mentioned above for MMSCs. Mononuclear cells from peripheral blood (PBMCs) of healthy volunteers were isolated by Ficoll-Нistopaque gradient (ρ1,077), (Sigma, США) according to standard protocol.

Cryopreserved samples of mononuclear cells from umbilical cord blood (CBMCs) were obtained from the Stem cell bank Cryocenter (Moscow, Russia).

2.2. Permanent Expansion of Stromal Cells under Low Oxygen

MMSCs after isolation and fFBs after thawing were divided into two parts. The first was further expanded at 5% CO2 and 95% air (20% O2) in a CO2-incubator (Sanyo, Japan) (normoxia); the other at 5% O2, 5% CO2, 90% N2 (hypoxia) in a multigas incubator (Sanyo, Japan). After reaching 70-80% confluence, cells were sub-cultured and 2-4 passages of MMSCs and 5-10 passages of fFBs were used in experiments.

2.3. Co-culture of PBMCs and Stromal Cells

PBMCs were activated with PHA (10 µg/ml) and were seeded without stromal cells (monoculture) or on preformed layers of normoxic and hypoxic MMSCs and fFBs (70-80% confluence) at a ratio of 10:1 PBMCs/stroma, and not less than 1x106 PBMCs/ml. Cells were co-cultured in RPMI 1640 medium (MP Biomedicals, USA), supplemented with 10% inactivated FBS (Hyclone, USA), 250μg/ml amphotericin, 5μg/ml streptomycin, 5U/ml penicillin, and 2mM glutamine (MP Biomedicals, USA) for 72 hours in normoxia (20% O2) and hypoxia (5% O2). Then, PBMCs were harvested by rinsing with PBS and stained for FACS analysis as described below.

2.4. Co-culture of CBMCs and Stromal Cells

1x106/ml of CBMCs were added to preformed stromal layers and co-cultured for 72 hours in the same medium as PBMCs in normoxic and hypoxic conditions. Then, unattached CBMCs were carefully washed out and the suspension of CBMCs was examined for CFU-activity in colony-forming cell assay. Stromal cells with attached CBMCs were further cultured up to 14 days and then the formation of undifferentiated precursor colonies on stromal feeders was assessed after Crystal violet staining.

Cell-cell interactions were monitored using Nikon Eclipse Ti-U microscope equipped with a Color Digital Camera DS-Ri1. Images were saved and later processed with NIS-Elements Auto Research software (Nikon Instruments, Japan).

2.5. FACS Analysis

For immunophenotyping of stromal cells, antibodies against the following antigens were used: CD34, CD45, CD54, CD90, CD105, CD106, CD117(c-kit) , HLA-ABC, HLA-DR and vimentin.

To identify lymphocyte types, antibodies against CD3+ (Т cells), CD3-/CD19+ (В cells), CD3-/16+/56+ (NК cells) were applied. Activated lymphocytes were recognized with anti-HLA-DR and anti-CD25 antibodies. All antibodies were directly conjugated to FITC or PE (all BD Biosciences, USA).

Fluorescence was measured with Epics XL cytofluorimeter using the manufacturer’s System II software for acquisition, analysis and for the creation of figures (Beckman Coulter, USA).

2.6. Colony-forming Cell (CFC) Assay

Freshly thawed CBMCs and cells after 72 hours co-culture with stromal cells (50x103 cells/ml) were cultured in methylcellulose-based medium MetoCult Н4534 (StemCells, USA) according to the manufacturer’s protocol at 20% and 5% O2. After 14 days, the number of CFCs was calculated.

2.7. Statistical Analysis

All data were derived from at least three independent experiments. Data are presented as mean ± standard error of the mean (M+m). Statistical comparisons were performed using the Student’s two-tailed t-test (unpaired/paired) in an Excel program. A P-value less than 0.05 was considered statistically significant.

3. Results

3.1. Immunophenotype of MMSCs vs. fFBs

Adipose tissue-derived MMSCs used in this work met the criteria for immunophenotypic identification of MMSCs [9] (Table 1). The analysis of the fFBs phenotype with the same antibody panel showed the virtual identity of the CD profile (Table 1), although fFBs and MMSCs were isolated from different tissues. The vast majority of MMSCs and fFBs had MMSC markers СD90 and СD105. All cells were positive on class-I major histocompatibility complex (HLA-ABC) antigen and had no class-II antigen (HLA-DR); they also contained vimentin, an intermediate filament common to cells of mesenchymal origin. Cells with the hematopoietic cell markers (СD34, СD45, HLA-DR) were few if any. It should be noted that reduced oxygen (5% vs. ambient 20%) in culture medium had no effect on the stromal cell immunoprofile.

Table 1. Expression of mesenchymal stem cell/progenitor markers in stromal cells

3.2. Immunomodulating Properties

Human lymphocyte types and activation in co-culture with stromal cells. The distribution of human lymphocyte types (T, B and NK cells) and T cell activation were analyzed after 72 hours of co-culture of PHA-activated PBMCs with stromal cells. All effects were normalized on respective values for PHA-PBMCs in monoculture and presented as a fold changes (Table 2). Co-cultures with stromal cells either had no affect (in the case of fFBs) or caused a slight reduction of the T-cell share (in case of MMSCs). The percentage of B cells increased and was more pronounced in the presence of MMSCs. The proportion of NK cells increased also; in NK case this effect was more significant in co-culture with fFBs. The increase in B cells was more and in NK less pronounced at 5% О2 as compared with the 20% O2, regardless of the stromal cell type. The activation of T cells was suppressed both in MMSC/PBMC and fFB/PBMC co-cultures. In case of CD3+/HLA-DR+ cells, the drop was more significant at 5% O2. The number of CD3+/CD25+ cells was similarly diminished in MMSC/PBMCs at 20% and 5% О2, and this effect was more pronounced (up to 40%) than in fFB/PBMCs. The decrease in CD3+/CD25+cells was not revealed after fFB/MCs co-culture under hypoxia.

Table 2. Lymphocyte types and activation after co-culture with stromal cells under different О2 conditions

Therefore, co-culture with stromal cells provoked the alteration in PHA-activated lymphocyte types as well as T cell activation. In the presence of fFBs, the percentage of NK cells was more and B cells less in comparison with same types in MMSC/MC co-culture. MMSCs and fFBs equally suppressed the population of HLA-DR-positive lymphocytes; however, the presence of fFBs had a little (20% О2) or no (5% О2) effect on CD25-expressing cells.

3.3. Hematopoiesis-supporting Properties

Colony forming cell (CFC) evaluation. To characterize the ability of stromal cells to maintain hematopoietic progenitors, in vitro colony forming activity was assessed in the initial cord blood MCs (CBMCs) and in the non-attached fraction of these cells after 72 hours of co-culture with MMSCs and fFBs. Initial CBMCs formed 25% more colonies at 5% О2 (Figure 1 (1)). Following 72 hours of co-culture with MMSCs, CBMCs retained the CF-potential, which was again more pronounced after co-culture at 5% О2 (Figure 1 (2)). The CF-activity was attenuated in CBMCs after co-culture with fFBs. This effect was particularly evident after hypoxic co-culture (Figure 1 (3)).

Figure 1. Colony- formation efficiency of CBMCs in MetoCult H4534

Formation of progenitor colonies on stromal layers. The part of CBMCs remained adhered to the stromal cells after 72 hours of co-culture (Figure 2 а-d). During the ensuing cultivation, these cells were able to form colonies of undifferentiated progenitors. 10 days later, these colonies were found on MMSCs and were not detected on fFBs (Figure 3 а-d), regardless of the О2 concentration in the medium.

Figure 2. CBMCs adhesion on stromal cells after 72 hours of co-colture

To sum up, umbilical cord blood hematopoietic progenitors retained the ability to form colonies in the semi-solid medium after co-culture with stromal cells. The CFU-activity after co-culture with fFBs was noticeably less when compared with initial CBMCs and co-cultured with MMSCs. CBMCs adhered to the MMSCs formed colonies of undifferentiated progenitors both at 20% and 5% О2; no colony was detected on the fFBs monolayer.

Figure 3. Stromal monolayers after 14 days of co-culture with CBMCs

4. Discussion

In the present paper we have compared some aspects of immunomodulating and hematopoiesis-supporting activity of two types of human stromal cells: adipose tissue derived MMSCs and fetal FBs. These properties appeared to be different in MMSCs and fFBs to some extent despite the fact that both cell types are low differentiated cells of mesenchymal origin.

The histogenetic relationship of FBs and MMSCs is still not fully elucidated. Stromal cells currently defined as MSCs were isolated by Friedenstein et al. [9] from bone marrow and termed “fibroblast-like cells”. The main features of these cells were the ability to adhere to substrate, to form colonies of progenitor cells (CFU-F) and to differentiate both in vivo and in vitro into other types of mesenchymal cells (adipocytes, osteoblasts, and chondroblasts). Later on, these cells were termed multipotent mesenchymal stem (stromal) cells (MMSCs) and much effort was spent to establish the “degree of kinship” between FBs and MMSCs [10, 11]. Today, MMSCs and FBs can be isolated from a large variety of tissues [12, 13]. It was found that, despite the diversity of sources, it is very difficult to distinguish MMSCs from FBs using the morphologic and immunophenotype criteria. All surface antigens used to identify MMSCs are also present on FBs [14, 15]. This finding is supported by our results on similar immunoprofile of human adipose tissue-derived MMSCs and human fetal FBs. The capacity for multilineage differentiation - a key MMSCs property, and immunosuppression are regarded as specialized functions arising from their low differentiated multipotent nature [14, 16]. However, the ontogenetic studies [17, 18] provided evidence suggesting that FBs are one of the most primitive cells of adult tissues. This gives a reason to suppose that FBs can share the same MMSC multipotent properties, particularly with regard to effects on the immune cells and hematopoietic progenitors’ maintenance.

MMSC immunomodulation activity now is well recognized. Thus, there is a clear demonstration that co-culture with MMSCs reduces allogenic T-lymphocyte proliferation, induces T-cell anergy and apoptosis, modulates cytokines production by immunocompetent cells, and inhibits T-cell activation and also maturation of dendritic cells. This immunomodulation is antigen-nonspecific and mediated by several soluble factors such as TGF-β, PGE2 and tryptophan metabolites [1, 2, 3]. Data on FBs are less consistent. It has long been shown that these cells can take on the role of alternative antigen-presenting cells activating or suppressing T-lymphocytes [4, 19] and mediating indirect anti-proliferating effects [20]. Still, there exists an opinion that stromal cells like FBs do not possess the immunosuppressive activity [14]. Nonetheless, it can be surmised that the immunomodulation properties are common to the stromal cells.

We have revealed an increase in NK and B cell percentages in suspensions of PHA-activated PBMCs after co-culture with both stromal cells. However, the increase in NK was more substantial in the presence of fFBs, whereas the increase of B cell proportion was more pronounced with MMSCs. In addition, the pattern of T-cell suppression was also different. The percentage of HLA-DR-positive cells was equally reduced after co-culture with MMSCs and fFBs. However, the fFBs impact on CD25-expression was weak (20% О2) or none (5% О2). That is, MMSCs suppressed expression T cells with both early (CD25) and late (HLA-DR) activation markers in normoxic and hypoxic conditions. In co-culture with fFBs, T cells with both activation markers were inhibited at 20% О2 and of late HLA-DR only at 5% О2.

The case of the fluctuation in lymphocyte types during co-culture with stromal cells has not yet been fully resolved. It is well known that activated Т cells adhere to the stromal layer forming the high specific cell-to-cell contacts [21, 22] and are even able to migrate into the space beneath the cells and back onto the stroma surface [21]. Recently we have shown that, in contrast to inactivated immune cells, PHA-activated PBMCs have effectively adhered to MMSCs and spread on their surface, and were able to transmigrate under stromal cells. This interaction involves at least one of the highly specific ligand-receptor paths mediated by ICAM-1 [23]. It can be assumed that the elevation of B and NK proportions in unattached PBMCs can be associated with the predominant adhesion of activated T cells. In addition, our data on the T cells’ suppression after co-culture with stromal cells may be also caused by peculiarities of activated lymphocytes’ «interplay» with MMSCs and fFBs.

At present, the use of stromal cells as feeders for hematopoietic cell expansion ex vivo is the routine cell culture practice [24, 25]. Initially, the feeder for hematopoietic cells consisted of a total population of adhesive marrow cells including stromal, endothelial and reticular cells, fibroblasts, pre-adipocytes, etc. This system was called “Dexter’s culture” [24]. Afterwards, HSC expansion on purified feeder cells such as FBs [26], stromal cells harvested from Dexter’s cultures MS-5 [27, 28] and MS-K [27] came into use; finally, MMSCs became of the primary choice [29, 30, 31, 32]).

In the present study, we demonstrated that hematopoietic cells from human cord blood retain the CFC-activity in semi-solid medium after co-culture with stromal progenitors. We assayed the ability of CBMCs to form the colonies of progenitor cells on the stromal monolayers (MMSCs and fFBs) at different О2 concentrations in culture medium. It was found that the number of CFCs among CBMCs co-cultured with MMSCs was slightly less than among initial CBMCs. Progenitor colonies were formed on the MMSC monolayer both at 20% and 5% О2. The CFC number after co-culture with fFBs was noticeably less in comparison with initial CBMCs and those co-cultured with MMSCs; no colony was detected on the fFBs monolayer. These data are in agreement with the earlier observations of Wagner et al. [30] who demonstrated the enhanced CD34+ cells hematopoiesis-supportive capacity of human bone marrow MMSCs than FB HS68 cell line. Today, most protocols for ex vivo expansion of hematopoietic cells preferentially employ MMSCs. However, comparison of the data from different studies is very complicated. This is due in part to differences in the experimental design. For instance, some laboratories irradiate a stromal supporting layer [26, 30, 32]. In this study we used intact pre-monolayer stromal cells as a feeder, as in [29]. Naturally, the profile of secreted biologically active substances will vary with the technique of supporting layer preparation. Besides, stromal and hematopoietic cells are co-cultured in a huge variety of media (i.e. with and without cytokines, chemokines and growth factors). The standard cocktail of stem cell growth factor (SCF), FL-3 ligand (FL3) and thrombopoietin (TPO) in addition to stroma feeder raises the effectiveness of hematopoietic cell expansion significantly [29, 33]. Nevertheless, these expensive growth media are not economical for clinical needs; therefore, preference can be given to intrinsic biologically active mediators produced by stromal cells. Using the conventional culture medium for stromal cell expansion (low glucose DMEM with standard supplements) in a 14-day experiment, we observed a better potential of MMSCs but not fFBs for maintaining hematopoietic cells from human umbilical cord blood. It is possible that the addition of growth factors or the extension of the experiment duration could help to reveal hematopoiesis-supportive potential of fFBs. It can be assumed that hematopoiesis-inducing capacities of stromal cells can vary in extent and time of realization and depend on microenvironmental parameters.

5. Conclusions

In conclusion, the stromal cells from different sources like human MMSCs from the stromal-vascular fraction of adipose tissue and fetal FBs have similar but not identical properties which can be considered a manifestation of their stromal and immunosuppressive potential. In addition, the partial oxygen pressure is an important physical factor that also modifies the results of cell-cell interactions and, therefore, should be taken into account when defining methodical approaches with regard to the use of stromal cells for the needs of regenerative medicine.

List of Abbreviations

MMSCs: multipotent mesenchymal stromal cells; fFBs: fetal fibroblasts; PBMCs: mononuclear cells from peripheral blood; CBMCs: mononuclear cells from umbilical cord blood; FCS: fetal calf serum; CFC, CFU: colony forming cell, colony forming unit; FACS: fluorescent activated cell sorting.

Competing Interests

The authors declare they have no competing interests.

Acknowledgements

This study was supported in part by a grant from the Basic Research Program #7 of Presidium of the Russian Academy of Science. We sincerely thank Dr. Olga V Grigorieva for assistance with co-culture experiments.

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