Suppression of in vitro murine T cell proliferation by human adipose tissue-derived mesenchymal stem cells is dependent mainly on cyclooxygenase-2 expression.
10.5115/acb.2013.46.4.262
- Author:
Jin Hee KIM
1
;
Yong Taek LEE
;
Jun Man HONG
;
Young Il HWANG
Author Information
1. Department of Anatomy, Seoul National University College of Medicine, Seoul, Korea. hyi830@snu.ac.kr
- Publication Type:In Vitro ; Original Article
- Keywords:
Mesenchymal stem cells;
Humans;
Cyclooxygenase-2;
Immunomodulation
- MeSH:
Adipose Tissue;
Animals;
Cell Proliferation*;
Coculture Techniques;
Cyclooxygenase 2*;
Cytokines;
Humans*;
Immunomodulation;
Indoleamine-Pyrrole 2,3,-Dioxygenase;
Interferon-gamma;
Mesenchymal Stromal Cells*;
Mice;
Models, Animal;
T-Lymphocytes;
Tumor Necrosis Factor-alpha
- From:Anatomy & Cell Biology
2013;46(4):262-271
- CountryRepublic of Korea
- Language:English
-
Abstract:
Mesenchymal stem cells (MSCs) of human origin have been frequently applied to experimental animal models to evaluate their immunomodulatory functions. MSCs are known to be activated by cytokines from T cells, predominantly by interferon-gamma (IFN-gamma), in conjunction with other cytokines such as tumor necrosis factor-alpha (TNF-alpha) and interlukin-1beta. Because IFN-gamma is not cross-reactive between human and mouse species, the manner in which human MSCs administered in experimental animals are activated and stimulated to function has been questioned. In the present study, we established MSCs from human adipose tissue. They successfully suppressed the proliferation of not only human peripheral blood mononuclear cells but also mouse splenic T cells. When these human MSCs were stimulated with a culture supernatant of mouse T cells or recombinant murine TNF-alpha, they expressed cyclooxygenase-2 (COX-2), but not indoleamine 2,3-dioxygenase. The dominant role of COX-2 in suppressing mouse T cell proliferation was validated by the addition of COX-2 inhibitor in the co-culture, wherein the suppressed proliferation was almost completely recovered. In conclusion, human MSCs in a murine environment were activated, at least in part, by TNF-alpha and mainly used COX-2 as a tool for the suppression of in vitro T cell proliferation. These results should be considered when interpreting results for human MSCs in experimental animals.
