Phosphoinositide 3-kinase in T cell activation and survival

被引:48
作者
Okkenhaug, K [1 ]
Bilancio, A
Emery, JL
Vanhaesebroeck, B
机构
[1] Babraham Inst, Lab Lymphocyte Signalling & Dev, Mol Immunol Programme, Cambridge CB2 4AT, England
[2] Ludwig Inst Canc Res, Cell Signalling Grp, London W1W 7BS, England
[3] UCL, Dept Biochem & Mol Biol, London WC1E 6BT, England
关键词
CD28; co-stimulation; p110; delta; phosphoinositide 3-kinase (PI3K); T cell receptor;
D O I
10.1042/BST0320332
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
PI3Ks (phosphoinositide 3-kinases) regulate diverse signalling pathways involved in growth, proliferation, survival, differentiation and metabolism. in T cells, PI3Ks can be activated by a number of different receptors, including the TcR (T cell receptor), co-stimulatory receptors, cytokine receptors and chemokine receptors. However, the specific roles of PI3Ks downstream of these receptors vary. An inactivating mutation in the leucocyte-specific PI3K isoform p110delta results in impaired TcR-dependent proliferation under circumstances where CD28 co-stimulation is blocked or not required. Recruitment and activation of PI3K by CD28 promotes survival by inducing increased expression of BCl-X(L). However, CD28 engages additional signals that regulate proliferation and interleukin-2 production independently of PI3K. Thus a model emerges whereby PI3K is involved in both TcR and CD28 signalling, but each receptor may only exploit a subset of the signalling pathways potentially controlled by PI3K activation.
引用
收藏
页码:332 / 335
页数:4
相关论文
共 42 条
[1]   Proliferative defect and embryonic lethality in mice homozygous for a deletion in the p110α subunit of phosphoinositide 3-kinase [J].
Bi, L ;
Okabe, I ;
Bernard, DJ ;
Wynshaw-Boris, A ;
Nussbaum, RL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (16) :10963-10968
[2]   Early embryonic lethality in mice deficient in the p110β catalytic subunit of PI 3-kinase [J].
Bi, L ;
Okabe, I ;
Bernard, DJ ;
Nussbaum, RL .
MAMMALIAN GENOME, 2002, 13 (03) :169-172
[3]   T cell receptor (TCR) interacting molecule (TRIM), a novel disulfide-linked dimer associated with the TCR-CD3-ζ complex, recruits intracellular signaling proteins to the plasma membrane [J].
Bruyns, E ;
Marie-Cardine, A ;
Kirchgessner, H ;
Sagolla, K ;
Shevchenko, A ;
Mann, M ;
Autschbach, F ;
Bensussan, A ;
Meuer, S ;
Schraven, B .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (03) :561-575
[4]   Cutting edge:: Distinct motifs within CD28 regulate T cell proliferation and induction of Bcl-XL [J].
Burr, JS ;
Savage, NDL ;
Messah, GE ;
Kimzey, SL ;
Shaw, AS ;
Arch, RH ;
Green, JM .
JOURNAL OF IMMUNOLOGY, 2001, 166 (09) :5331-5335
[5]   T cell antigen receptor signal transduction pathways [J].
Cantrell, D .
ANNUAL REVIEW OF IMMUNOLOGY, 1996, 14 :259-274
[6]   Sustained and dynamic inositol lipid metabolism inside and outside the immunological synapse [J].
Costello, PS ;
Gallagher, M ;
Cantrell, DA .
NATURE IMMUNOLOGY, 2002, 3 (11) :1082-1089
[7]   Proteolysis-independent regulation of PI3K by Cbl-b-mediated ubiquitination in T cells [J].
Fang, DY ;
Liu, YC .
NATURE IMMUNOLOGY, 2001, 2 (09) :870-875
[8]  
Ferguson SE, 1996, J IMMUNOL, V156, P4576
[9]   The CD28 signaling pathway regulates glucose metabolism [J].
Frauwirth, KA ;
Riley, JL ;
Harris, MH ;
Parry, RV ;
Rathmell, JC ;
Plas, DR ;
Elstrom, RL ;
June, CH ;
Thompson, CB .
IMMUNITY, 2002, 16 (06) :769-777
[10]   The T-cell receptor regulates Akt (protein kinase B) via a pathway involving Rac1 and phosphatidylinositide 3-kinase [J].
Genot, EM ;
Arrieumerlou, C ;
Ku, G ;
Burgering, BMT ;
Weiss, A ;
Kramer, IM .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (15) :5469-5478