Lian Xiaoming, Matthaeus Claudia, Kaßmann Mario, Daumke Oliver, Gollasch Maik
Experimental and Clinical Research Center-A Joint Cooperation Between the Charité-University Medicine Berlin and the Max Delbrück Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.
Max Delbrück Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.
Front Med (Lausanne). 2019 Jul 10;6:153. doi: 10.3389/fmed.2019.00153. eCollection 2019.
Caveolae, flask-shaped cholesterol-, and glycosphingolipid-rich membrane microdomains, contain caveolin 1, 2, 3 and several structural proteins, in particular Cavin 1-4, EHD2, pacsin2, and dynamin 2. Caveolae participate in several physiological processes like lipid uptake, mechanosensitivity, or signaling events and are involved in pathophysiological changes in the cardiovascular system. They serve as a specific membrane platform for a diverse set of signaling molecules like endothelial nitric oxide synthase (eNOS), and further maintain vascular homeostasis. Lack of caveolins causes the complete loss of caveolae; induces vascular disorders, endothelial dysfunction, and impaired myogenic tone; and alters numerous cellular processes, which all contribute to an increased risk for hypertension. This brief review describes our current knowledge on caveolae in vasculature, with special focus on their pathophysiological role in hypertension.
小窝是烧瓶状、富含胆固醇和糖鞘脂的膜微区,包含小窝蛋白1、2、3以及几种结构蛋白,特别是窖蛋白1-4、EHD2、pacsin2和发动蛋白2。小窝参与脂质摄取、机械敏感性或信号转导等多种生理过程,并涉及心血管系统的病理生理变化。它们作为多种信号分子(如内皮型一氧化氮合酶(eNOS))的特定膜平台,并进一步维持血管稳态。小窝蛋白的缺失会导致小窝完全丧失;引发血管疾病、内皮功能障碍和肌源性张力受损;并改变众多细胞过程,所有这些都增加了患高血压的风险。本简要综述描述了我们目前对血管中微窝的认识,特别关注它们在高血压中的病理生理作用。