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Editorial

Mesenchymal stem cells in arthritis: role of bone marrow microenvironment

Christian Jorgensen

Author Affiliations

Inserm, U844, Montpellier F-34091, France

Université Montpellier 1, UFR de Médecine, Montpellier F-34000, France

Arthritis Research & Therapy 2010, 12:135  doi:10.1186/ar3105


See related research article by Mohanty et al., http://arthritis-research.com/content/12/4/R149


The electronic version of this article is the complete one and can be found online at: http://arthritis-research.com/content/12/4/135


Published:23 August 2010

© 2010 BioMed Central Ltd.

Abstract

Based on their capacity to suppress immune responses, multipotent mesenchymal stromal cells (MSCs) are intensively studied for regenerative medicine. Moreover, MSCs are potent immunomodulatory cells that occur through the secretion of soluble mediators including nitric oxide, transforming growth factor beta, and HLAG5. The MSCs, however, are also able to express inflammatory mediators such as prostaglandin E2 or IL-6. MSCs in the bone marrow are in close contact with T cells and B cells, and they regulate immunological memory by organizing defined numbers of dedicated survival niches for plasma cells and memory T cells in the bone marrow. The role of MSCs in arthritis remains controversial - in some studies, murine allogeneic MSCs are able to decrease arthritis; in other studies, MSCs worsen the local inflammation. A recent paper in Arthritis Research and Therapy shows that bone marrow MSCs have decreased osteoblastic potential in rheumatoid arthritis, which may be related to chronic inflammation or to loss of expression of IL-1 receptor agonist. That article raises the importance of the bone marrow microenvironment for MSC biology.

Editorial

Mesenchymal stem cells or multipotent mesenchymal stromal cells (MSCs) have been identified in the bone marrow as well as in other tissues of the joint, including adipose tissue, synovial tissue, periosteum, perichondrium, and cartilage. These cells are characterized by their phenotype and their ability to dibranchiate into three lineages, chondrocytes, osteoblasts and adipocytes. Importantly, MSCs are also potent modulators of immune responses, exhibit healing capacities, improve angiogenesis and prevent fibrosis. The recent work of Mohanty and coworkers shows the changes in the bone marrow niche in the course of arthritis and the loss of osteoblastic differentiation in this model [1].

Mesenchymal stem cells are present in the arthritic joint

MSCs are defined according to three criteria: their property to adhere to plastic, their phenotype (CD73+, CD90+, CD105+, CD45-, CD14-, CD11b-, CD34-) and their capacity to differentiate into three lineages: chondrocytes, osteoblasts and adipocytes [2]. Besides these factors, MSCs display a broader differentiation potential. They can differentiate into myocytes, tendinocytes, ligamentocytes, cardiomyocytes, and other cell types [3]. Their differentiation potential is largely dependent on environmental factors; in particular, specific growth factors - but, as an example, hypoxia and the three-dimensional environment are also pivotal factors that probably help to support the chondrocytic phenotype. MSCs have been identified in the bone marrow, but also in other tissues of the joint including adipose tissue, periosteum, perichondrium, synovial tissue and cartilage [4-7].

Immunomodulatory effects of mesenchymal stem cells

In addition to their potential for tissue repair, MSCs are potent modulators of immune responses, having anti-proliferative and anti-inflammatory capacities. Although terminally differentiated stromal cells, such as fibroblasts, also share some immunosuppressive activities with MSCs, as shown by their ability to suppress in vitro T-cell proliferation [8], they do not exert in vivo the suppressive effect mediated by MSCs. MSC-mediated immunosuppressant requires their previous activation by immune cells through proinflammatory cytokines IFNγ with TNFα or IL-1β [9]. Moreover, other molecules including indoleamine-2,3-dioxygenase, heme oxidase as well as HLAG5 have been involved in MSC-mediated immunosuppression.

MSCs, however, are also able to express inflammatory mediators such as prostglandin E2 or IL-6. The production of this enzymatic product of arachidonic acid metabolism is enhanced in MSCs upon TNFα or IFNγ stimulation. This may explain why in a particular inflammatory environment MSCs may have a paradoxal effect on immune cells. In the bone marrow niche, another example of the role of MSCs is the production of receptor activator for NF-κB ligand (RankL) and of osteoprotegerin, which will stimulate osteoclast formation from hematopoietic precursor cells and will inhibit bone formation, respectively. Moreover, MSCs regulate immunological memory by organizing defined numbers of dedicated survival niches for plasma cells and memory T cells in the bone marrow. A distinct subpopulation of MSCs, characterized by the expression of CXCL12 and vascular cell adhesion molecule-1, might provide a survival niche for memory plasma cells [10]. In contrast, another fraction of CXCL12-negative bone marrow MSCs expresses IL-7. These cells are in close contact with memory CD4+ T cells and keep the T cells quiescent through the effect of IL-7. These results suggest heterogeneity of MSCs in terms of immune and hematopoietic functions, but also suggest that MSCs play a key role to maintain immune homeostasis.

Mesenchymal stem cells and autoimmunity

In rheumatoid arthritis, using the experimental collage-induced arthritis model, contrasting results are reported. A single injection of MSCs was shown to prevent the occurrence of severe arthritis, which was associated with a decrease in serum proinflammatory cytokines [11]. We have shown that the allogeneic C3H10T1/2 MSC line did not exert a beneficial effect on collagen-induced arthritis [12]. As in other autoimmune models, MSCs were not observed in the target organ. Zappia and collaborators reported the therapeutic efficacy of MSCs in the experimental autoimmune encephalomyelitis murine model of multiple sclerosis [13]. In this model, MSCs decreased the clinical signs associated with demyelinization when injected before or at the onset of disease. The same results were observed in a model of autoimmune diabetes, where MSC injection induced a decrease in mesangial thickening and in macrophage infiltration, resulting in the prevention of pancreatic injury [14].

Stromal cells are no longer second citizens but are first-line players. They appear as major regulatory cells in skeletal tissues controlling inflammation, immune response, fibrosis and tissue regeneration. A better understanding of the interactions between stromal cells and immune cells is required for therapeutic applications and to validate the strong potential of MSCs in rheumatologic diseases. The work presented by Mohanty and colleagues underlines the link between osteoporosis, inflammation and MSCs. The in vivo behavior of MSCs in the context of pathological situations remains to be further studied in rheumatoid arthritis.

Abbreviations

IFN: interferon; IL: interleukin; MSC: mesenchymal stromal cell; NF: nuclear factor; TNF: tumor necrosis factor.

Competing interests

The author declares that they have no competing interests.

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