Relevance of CD6-mediated interactions in T cell activation and proliferation

被引:120
作者
Gimferrer, I
Calvo, M
Mittelbrunn, M
Farnós, M
Sarrias, MR
Enrich, C
Vives, J
Sánchez-Madrid, F
Lozano, F
机构
[1] Hosp Clin Barcelona, Serv Immunol, Inst Invest Biomed August Pi & Sunyer, Barcelona 08036, Spain
[2] Univ Barcelona, Fac Med, Inst Invest Biomed August Pi & Sunyer, Dept Cellular Biol, Barcelona 7, Spain
[3] Univ Autonoma Madrid, Hosp Princesa, Serv Inmunol, Madrid, Spain
关键词
D O I
10.4049/jimmunol.173.4.2262
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD6 is a cell surface receptor expressed on immature thymocytes and mature T and B1a lymphocytes. The ultimate function of CD6 has not been deciphered yet, but much evidence supports a role for CD6 in T cell activation and differentiation. In this study, we show that a fraction of CD6 molecules physically associates with the TCR/CD3 complex by coimmunoprecipitation, cocapping, and fluorescence resonance energy transfer experiments. Image analysis of Ag-specific T-APC conjugates demonstrated that CD6 and its ligand, activated leukocyte cell adhesion molecule (CD166), colocalize with TCR/CD3 at the center of the immunological synapse, the so-called central supramolecular activation cluster. The addition of a soluble rCD6 form significantly reduced the number of mature Ag-specific T-APC conjugates, indicating that CD6 mediates early cell-cell interactions needed for immunological synapse maturation to proceed. This was in agreement with the dose-dependent inhibition of CD3-mediated T cell proliferation induced by soluble rCD6. Taken together, our data illustrate the important role played by the intra- and intercellular molecular interactions mediated by CD6 during T cell activation and proliferation processes.
引用
收藏
页码:2262 / 2270
页数:9
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