Sverdlov Maria, Shajahan Ayesha N, Minshall Richard D
Department of Pharmacology, Center for Lung and Vascular Biology, University of Illinois, College of Medicine at Chicago, Chicago, IL 60612, USA.
J Cell Mol Med. 2007 Nov-Dec;11(6):1239-50. doi: 10.1111/j.1582-4934.2007.00127.x.
Caveolae are flask-shaped plasma membrane invaginations that mediate endocytosis and transcytosis of plasma macromolecules, such as albumin, insulin and low-density lipoprotein (LDL), as well as certain viruses, bacteria and bacterial toxins. Caveolae-mediated transcytosis of macromolecules is critical for maintaining vascular homeostasis by regulating the oncotic pressure gradient and tissue delivery of drugs, vitamins, lipids and ions. Entrapment of cargo within caveolae induces activation of signalling cascades leading to caveolae fission and internalization. Activation of Src tyrosine kinase is an early and essential step that triggers detachment of loaded caveolae from the plasma membrane. In this review, we examine how Src-mediated phosphorylation regulates caveolae-mediated transport by orchestrating the localization and activity of essential proteins of the endocytic machinery to regulate caveolae formation and fission.
小窝是烧瓶状的质膜内陷结构,介导血浆大分子(如白蛋白、胰岛素和低密度脂蛋白(LDL))以及某些病毒、细菌和细菌毒素的内吞作用和转胞吞作用。小窝介导的大分子转胞吞作用对于通过调节胶体渗透压梯度以及药物、维生素、脂质和离子的组织递送维持血管稳态至关重要。货物被困在小窝内会诱导信号级联反应的激活,导致小窝裂变和内化。Src酪氨酸激酶的激活是触发负载小窝从质膜脱离的早期关键步骤。在本综述中,我们研究了Src介导的磷酸化如何通过协调内吞机制关键蛋白的定位和活性来调节小窝形成和裂变,从而调控小窝介导的运输。