Matthaeus Claudia, Taraska Justin W
Biochemistry and Biophysics Center, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD, United States.
Front Cell Dev Biol. 2021 Jan 21;8:614472. doi: 10.3389/fcell.2020.614472. eCollection 2020.
Caveolae are 70-100 nm diameter plasma membrane invaginations found in abundance in adipocytes, endothelial cells, myocytes, and fibroblasts. Their bulb-shaped membrane domain is characterized and formed by specific lipid binding proteins including Caveolins, Cavins, Pacsin2, and EHD2. Likewise, an enrichment of cholesterol and other lipids makes caveolae a distinct membrane environment that supports proteins involved in cell-type specific signaling pathways. Their ability to detach from the plasma membrane and move through the cytosol has been shown to be important for lipid trafficking and metabolism. Here, we review recent concepts in caveolae trafficking and dynamics. Second, we discuss how ATP and GTP-regulated proteins including dynamin and EHD2 control caveolae behavior. Throughout, we summarize the potential physiological and cell biological roles of caveolae internalization and trafficking and highlight open questions in the field and future directions for study.
小窝是直径70 - 100纳米的质膜内陷结构,在脂肪细胞、内皮细胞、肌细胞和成纤维细胞中大量存在。它们的球状膜结构域由包括小窝蛋白、窖蛋白、Pacsin2和EHD2在内的特定脂质结合蛋白所表征和形成。同样,胆固醇和其他脂质的富集使小窝成为一个独特的膜环境,支持参与细胞类型特异性信号通路的蛋白质。它们从质膜脱离并在细胞质中移动的能力已被证明对脂质运输和代谢很重要。在这里,我们综述了小窝运输和动态变化的最新概念。其次,我们讨论了包括发动蛋白和EHD2在内的ATP和GTP调节蛋白如何控制小窝行为。在整个过程中,我们总结了小窝内化和运输的潜在生理和细胞生物学作用,并突出了该领域的开放性问题和未来研究方向。