Department of Genetics and Genomic Sciences, Mount Sinai School of Medicine, Icahn Medical Institute, New York, NY 10029, USA.
FEBS Lett. 2010 May 3;584(9):1895-900. doi: 10.1016/j.febslet.2009.11.083. Epub 2009 Nov 26.
Acid sphingomyelinase (ASM) plays an important role in normal membrane turnover through the hydrolysis of sphingomyelin, and is one of the key enzymes responsible for the production of ceramide. ASM activity is deficient in the genetic disorder Types A and B Niemann-Pick disease (NPD). ASM knockout (ASMKO) mice were originally constructed to study this disorder, and numerous defects in ceramide-related signaling have been shown. Studies in these mice have further suggested that ASM may be involved in the pathogenesis of several common diseases through the reorganization of membrane microdomains. This review will focus on the role of ASM in membrane biology, with a specific emphasis on what a rare genetic disorder (NPD) has taught us about more common events.
酸性鞘磷脂酶 (ASM) 通过水解鞘磷脂在正常的膜周转中发挥重要作用,是负责产生神经酰胺的关键酶之一。遗传性疾病 A 型和 B 型尼曼-皮克病 (NPD) 中存在 ASM 活性缺陷。ASM 基因敲除 (ASMKO) 小鼠最初是为了研究这种疾病而构建的,并且已经显示出与神经酰胺相关的信号转导存在许多缺陷。这些小鼠的研究进一步表明,ASM 可能通过膜微区的重组参与几种常见疾病的发病机制。本综述将重点讨论 ASM 在膜生物学中的作用,特别强调罕见遗传疾病 (NPD) 告诉我们的关于更常见事件的信息。