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渥曼青霉素,一种磷脂酰肌醇3激酶抑制剂,可阻断抗原介导的而非CD3单克隆抗体诱导的小鼠CD4 + T细胞活化。

Wortmannin, a phosphatidylinositol 3-kinase inhibitor, blocks antigen-mediated, but not CD3 monoclonal antibody-induced, activation of murine CD4+ T cells.

作者信息

Shi J, Cinek T, Truitt K E, Imboden J B

机构信息

Department of Medicine and San Francisco General Hospital, University of California, 94143, USA.

出版信息

J Immunol. 1997 May 15;158(10):4688-95.

PMID:9144481
Abstract

Perturbation of several distinct T cell molecules, including the CD3/TCR complex, CD7, and CD28, activates phosphatidylinositol 3-kinase (PI3-K), but a clear consensus on the role of PI3-K in T cell activation has yet to emerge. We report here that CD3 mAb-induced IL-2 production by CD4+ T cells from DO11.10 TCR-alphabeta-transgenic mice is refractory to the potent PI3-K inhibitor, wortmannin, demonstrating that activation under these conditions is independent of PI3-K. In marked contrast, wortmannin substantially inhibits IL-2 production elicited by Ag (OVA(323-339) peptide) presented by appropriate APCs (syngeneic B7+ B cell blasts) and blocks Ag-induced differentiation of naive CD4+ DO11.10 T cells into IL-4-producing cells. Wortmannin inhibits Ag-induced conjugate formation between T cells and B7+ B cell blasts. Because T cell activation by Ag requires stable interactions with APCs, this inhibitory effect on conjugate formation may underlie the ability of wortmannin to block Ag-induced IL-2 production and differentiation.

摘要

多种不同的T细胞分子,包括CD3/TCR复合物、CD7和CD28的扰动,可激活磷脂酰肌醇3激酶(PI3-K),但关于PI3-K在T细胞激活中的作用尚未形成明确的共识。我们在此报告,DO11.10 TCRαβ转基因小鼠的CD4+ T细胞由CD3单克隆抗体诱导产生白细胞介素-2(IL-2)对强效PI3-K抑制剂渥曼青霉素具有抗性,这表明在这些条件下的激活不依赖于PI3-K。与之形成显著对比的是,渥曼青霉素可显著抑制由合适的抗原呈递细胞(同基因B7+ B细胞母细胞)呈递的抗原(卵清蛋白(OVA(323-339))肽)引发的IL-2产生,并阻断抗原诱导的初始CD4+ DO11.10 T细胞分化为产生IL-4的细胞。渥曼青霉素可抑制抗原诱导的T细胞与B7+ B细胞母细胞之间的结合形成。由于抗原对T细胞的激活需要与抗原呈递细胞的稳定相互作用,这种对结合形成的抑制作用可能是渥曼青霉素阻断抗原诱导的IL-2产生和分化能力的基础。

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