Open AccessMesenchymal stem cells induce a weak immune response in the rat striatum after allo or xenotransplantation
Author(s) -
Rossignol Julien,
Boyer Cécile,
Thinard Reynald,
Remy Séverine,
Dugast AnneSophie,
Dubayle David,
Dey Nicolas D.,
Boeffard Françoise,
Delecrin Joël,
Heymann Dominique,
Vanhove Bernard,
Anegon Ignacio,
Naveilhan Philippe,
Dunbar Gary L.,
Lescaudron Laurent
Publication year - 2009
Publication title -
journal of cellular and molecular medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.44
H-Index - 130
eISSN - 1582-4934
pISSN - 1582-1838
DOI - 10.1111/j.1582-4934.2008.00657.x
Subject(s) - mesenchymal stem cell , transplantation , immune system , biology , cd90 , xenotransplantation , immunology , stem cell , cd34 , microbiology and biotechnology , medicine
Mesenchymal stem cells (MSCs) have attracted attention for their potential use in regenerative medicine such as brain transplantation. As MSCs are considered to be hypoimmunogenic, transplanted MSCs should not trigger a strong host inflammatory response. To verify this hypothesis, we studied the brain immune response after transplantation of human or rat MSCs into the rat striatum and MSC fate at days 5, 14, 21 and 63 after transplantation. Flow cytometry analysis indicated that both MSCs express CD90 and human leucocyte antigen (MHC) class I, but no MHC class II molecules. They do not express CD45 or CD34 antigens. However, MSC phenotype varies with passage number. Human MSCs have mRNAs for interleukin (IL)‐6, IL‐8, IL‐12, tumour necrosis factor (TNF)‐α and TGF‐β 1 , whereas rat MSCs express IL‐6‐, IL‐10‐, IL‐12‐ and TGF‐β 1 ‐mRNAs. The quantification shows higher levels of mRNAs for the anti‐inflammatory molecules IL‐6 and TGF‐β 1 than for pro‐inflammatory cytokines IL‐8 and IL‐12; ELISA analysis showed no IL‐12 whereas TGF‐β 1 and IL‐6 were detected. Transplant size did not significantly vary between 14 and 63 days after transplantation, indicating an absence of immune rejection of the grafts. Very few mast cells and moderate macrophage and microglial infiltrations, observed at day 5 remained stable until day 63 after transplantation in both rat and human MSC grafts. The observations of very few dendritic cells, T αβ‐cells, and no T γδ‐lymphocytes, all three being associated with Tp rejection in the brain, support the contention that MSCs are hypoimmunogenic. Our results suggest that MSCs are of great interest in regenerative medicine in a (xeno)transplantation setting.