Marshansky Vladimir, Futai Masamitsu
Program in Membrane Biology, Center for Systems Biology, Simches Research Center, CPZN No. 8212, Massachusetts General Hospital, 185 Cambridge Street, Boston, MA 02114, USA.
Curr Opin Cell Biol. 2008 Aug;20(4):415-26. doi: 10.1016/j.ceb.2008.03.015. Epub 2008 May 27.
Vacuolar-type H+-ATPase (V-ATPase)-driven proton pumping and organellar acidification is essential for vesicular trafficking along both the exocytotic and endocytotic pathways of eukaryotic cells. Deficient function of V-ATPase and defects of vesicular acidification have been recently recognized as important mechanisms in a variety of human diseases and are emerging as potential therapeutic targets. In the past few years, significant progress has been made in our understanding of function, regulation, and the cell biological role of V-ATPase. Here, we will review these studies with emphasis on novel direct roles of V-ATPase in the regulation of vesicular trafficking events.
液泡型H⁺-ATP酶(V-ATP酶)驱动的质子泵浦和细胞器酸化对于真核细胞胞吐和胞吞途径的囊泡运输至关重要。最近,V-ATP酶功能缺陷和囊泡酸化缺陷已被确认为多种人类疾病的重要机制,并正在成为潜在的治疗靶点。在过去几年中,我们对V-ATP酶的功能、调节及其细胞生物学作用的理解取得了重大进展。在此,我们将回顾这些研究,重点关注V-ATP酶在调节囊泡运输事件中的新直接作用。