| Literature DB >> 23023221 |
Yong-Soo Lee1, Kyung-Jong Won, Sung-Won Park, Hyeon-Woo Lee, Bokyung Kim, Jin-Hoi Kim, Dong-Ku Kim.
Abstract
Mesenchymal stem cells (MSCs) have known to induce immunosuppressive properties by preventing T cell proliferation. However, it is remains unclear how MSCs inhibit T cell proliferation. To identify the factor that inhibits T cell proliferation, we conducted a cytokine array analysis of culture medium from a co-culture of MSCs and T cells and found that the chemokines, CXCL1, 2 and 3, were induced in T cells. MSCs also induced the expression of the CXCR2 receptor on T cell surface. Particularly, CXCL3 inhibited proliferation and increased apoptosis in T cells, which were reversed by CXCR2 inhibitor treatment. Moreover, CXCL3 decreased JAK2, STAT3, and AKT phosphorylation and these responses were also abolished by CXCR2 inhibitor treatment. MSCs suppressed the proliferation of T cells into tumor tissue. Collectively, these data demonstrate that MSCs directly regulate T cell proliferation by induction of CXCL3 chemokine and its receptor, CXCR2 on the surface in T cells.Entities:
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Year: 2012 PMID: 23023221 DOI: 10.1016/j.cellimm.2012.08.002
Source DB: PubMed Journal: Cell Immunol ISSN: 0008-8749 Impact factor: 4.868