Protein kinase Cθ in T cell activation

被引:304
作者
Isakov, N [1 ]
Altman, A
机构
[1] Ben Gurion Univ Negev, Fac Hlth Sci, Dept Microbiol & Immunol, IL-84105 Beer Sheva, Israel
[2] Ben Gurion Univ Negev, Canc Res Ctr, IL-84105 Beer Sheva, Israel
[3] La Jolla Inst Allergy & Immunol, Div Cell Biol, San Diego, CA 92121 USA
关键词
PKC theta; TCR/CD28; immune synapse; IL-2; NF-kappa B/AP-1;
D O I
10.1146/annurev.immunol.20.100301.064807
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The novel protein kinase C (PKC) isoform, PKCtheta, is selectively expressed in T lymphocytes and is a sine qua non for T cell antigen receptor (TCR)-triggered activation of mature T cells. Productive engagement of T cells by antigen-presenting cells (APCs) results in recruitment of PKCtheta to the T cell-APC contact area-the immunological synapse-where it interacts with several signaling molecules to induce activation signals essential for productive T cell activation and IL-2 production. The transcription factors NF-kappaB and AP-1 are the primary physiological targets of PKCtheta, and efficient activation of these transcription factors by PKCtheta requires integration of TCR and CD28 costimulatory signals. PKCtheta cooperates with the protein Ser/Thr phosphatase, calcineurin, in transducing signals leading to activation of JNK, NFAT, and the IL-2 gene. PKCtheta also promotes T cell cycle progression and regulates programmed T cell death. The exact mode of regulation and immediate downstream substrates of PKCtheta are still largely unknown. Identification of these molecules and determination of their mode of operation with respect to the function of PKCtheta will provide essential information on the mechanism of T cell activation. The selective expression of PKCtheta in T cells and its essential role in mature T cell activation establish it as an attractive drug target for immunosuppression in transplantation and autoimmune diseases.
引用
收藏
页码:761 / 794
页数:36
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