Osteodifferentiated Mesenchymal Stem Cells from Bone Marrow and Adipose Tissue Express HLA-G and Display Immunomodulatory Properties in HLA-Mismatched Settings: Implications in Bone Repair Therapy

Author:

Montespan Florent12,Deschaseaux Frédéric3,Sensébé Luc3,Carosella Edgardo D.12,Rouas-Freiss Nathalie12ORCID

Affiliation:

1. CEA, Institut des Maladies Emergentes et des Therapies Innovantes (IMETI), Service de Recherche en Hemato-Immunologie (SRHI), Hopital Saint-Louis, IUH, 1 avenue Claude Vellefaux, 75010 Paris, France

2. Universite Paris Diderot, Sorbonne Paris Cité, IUH, Hopital Saint-Louis, UMR_E5, IUH, 1, avenue Claude Vellefaux, 75010 Paris, France

3. Stromalab UMR UPS/CNRS 5273, EFS-Pyrénées-Méditerranée, U1031 Inserm, 31432 Toulouse, France

Abstract

Mesenchymal stem cells (MSCs) are multipotent cells that can be obtained from several sources such as bone marrow and adipose tissue. Depending on the culture conditions, they can differentiate into osteoblasts, chondroblasts, adipocytes, or neurons. In this regard, they constitute promising candidates for cell-based therapy aimed at repairing damaged tissues. In addition, MSCs display immunomodulatory properties through the expression of soluble factors including HLA-G. We here analyse both immunogenicity and immunosuppressive capacity of MSCs derived from bone marrow and adipose tissue before and after osteodifferentiation. Results show that HLA-G expression is maintained after osteodifferentiation and can be boosted in inflammatory conditions mimicked by the addition of IFN-γand TNF-α. Both MSCs and osteodifferentiated MSCs are hypoimmunogenic and exert immunomodulatory properties in HLA-mismatched settings as they suppress T cell alloproliferation in mixed lymphocyte reactions. Finally, addition of biomaterials that stimulate bone tissue formation did not modify MSC immune properties. As MSCs combine both abilities of osteoregeneration and immunomodulation, they may be considered as allogenic sources for the treatment of bone defects.

Publisher

Hindawi Limited

Subject

Immunology,General Medicine,Immunology and Allergy

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