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通过表达VIP21-小窝蛋白在淋巴细胞中从头形成小窝

De novo formation of caveolae in lymphocytes by expression of VIP21-caveolin.

作者信息

Fra A M, Williamson E, Simons K, Parton R G

机构信息

European Molecular Biology Laboratory, Heidelberg, Germany.

出版信息

Proc Natl Acad Sci U S A. 1995 Sep 12;92(19):8655-9. doi: 10.1073/pnas.92.19.8655.

Abstract

Caveolae are plasma membrane invaginations, which have been implicated in endothelial transcytosis, endocytosis, potocytosis, and signal transduction. In addition to their well-defined morphology, caveolae are characterized by the presence of an integral membrane protein termed VIP21-caveolin. We have recently observed that lymphocytes have no detectable VIP21-caveolin and lack plasma membrane invaginations resembling caveolae. Here we transiently express VIP21-caveolin in a lymphocyte cell line using the Semliki Forest virus expression system and show de novo formation of plasma membrane invaginations containing VIP21-caveolin. These invaginations appear homogeneous in size and morphologically indistinguishable from caveolae of nonlymphoid cells. Moreover, the glycosylphosphatidylinositol-anchored protein. Thy1, patched by antibodies, redistributes to the newly formed caveolae. Our results show that VIP21-caveolin is a key structural component required for caveolar biogenesis.

摘要

小窝是质膜内陷结构,与内皮细胞转胞吞作用、胞吞作用、液相胞饮作用及信号转导有关。除了其明确的形态外,小窝的特征还在于存在一种称为VIP21-小窝蛋白的整合膜蛋白。我们最近观察到淋巴细胞中检测不到VIP21-小窝蛋白,并且缺乏类似小窝的质膜内陷结构。在此,我们使用Semliki森林病毒表达系统在淋巴细胞系中瞬时表达VIP21-小窝蛋白,并显示出含有VIP21-小窝蛋白的质膜内陷结构的从头形成。这些内陷结构大小均匀,在形态上与非淋巴细胞的小窝无法区分。此外,经抗体捕捉的糖基磷脂酰肌醇锚定蛋白Thy1会重新分布到新形成的小窝中。我们的结果表明,VIP21-小窝蛋白是小窝生物发生所需的关键结构成分。

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