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CD2与微管蛋白的关联。细胞骨架在T细胞活化中作用的证据。

Association of CD2 with tubulin. Evidence for a role of the cytoskeleton in T cell activation.

作者信息

Offringa R, Bierer B E

机构信息

Division of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.

出版信息

J Biol Chem. 1993 Mar 5;268(7):4979-88.

PMID:8095265
Abstract

In addition to the antigen-specific T cell receptor, a number of other T cell surface molecules contribute to T cell adhesion and activation. CD2 is a 50-kDa glycoprotein found on the surface of human T lymphocytes which plays a role in T cell adhesion and stimulation. The intracellular mechanisms by which CD2 functions are, however, not fully defined. Here we show that the T cell surface molecule CD2 physically interacts with tubulin. This interaction appears to involve the membrane-proximal part of the cytoplasmic domain of the CD2 molecule, suggesting that CD2 binds to the tubulin fraction previously shown to be present in membranes. Stimulation of T cells with activating pairs of anti-CD2 antibodies, capable of initiating lymphokine production and T cell proliferation, disrupts the CD2-tubulin complexes, suggesting that the dynamic interaction of CD2 with tubulin may play a role in T cell activation.

摘要

除了抗原特异性T细胞受体外,许多其他T细胞表面分子也有助于T细胞的黏附和激活。CD2是一种在人T淋巴细胞表面发现的50 kDa糖蛋白,它在T细胞黏附和刺激中发挥作用。然而,CD2发挥功能的细胞内机制尚未完全明确。在这里,我们表明T细胞表面分子CD2与微管蛋白发生物理相互作用。这种相互作用似乎涉及CD2分子胞质结构域的膜近端部分,这表明CD2与先前已证明存在于膜中的微管蛋白部分结合。用能够启动淋巴因子产生和T细胞增殖的抗CD2抗体激活对刺激T细胞,会破坏CD2 - 微管蛋白复合物,这表明CD2与微管蛋白的动态相互作用可能在T细胞激活中发挥作用。

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