Clarke Christopher J, Snook Christopher F, Tani Motohiro, Matmati Nabil, Marchesini Norma, Hannun Yusuf A
Department of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, South Carolina 29425, USA.
Biochemistry. 2006 Sep 26;45(38):11247-56. doi: 10.1021/bi061307z.
The neutral sphingomyelinases (N-SMases) are considered major candidates for mediating the stress-induced production of ceramide, and N-SMase activity has been identified, characterized, and cloned from bacteria, yeast, and mammalian cells. Although the level of identity between these enzymes is low, a number of key residues thought to be involved in metal binding and catalysis are conserved. This has led to the suggestion of a common catalytic mechanism, and thus, these enzymes are considered to form an extended family of N-SMases. Despite considerable research into N-SMase activity in cell culture and various tissues, the lack, until recently, of molecular identification of specific N-SMase enzymes had precluded specific insights into the regulation, physiological, and pathological roles of these proteins. In this review, we summarize, for the first time, current knowledge of the N-SMase family, focusing on cloned members from bacteria, yeast, and mammalian cells. We also briefly consider the major future directions for N-SMase research which promises highly significant and specific insight into sphingolipid-mediated functions.
中性鞘磷脂酶(N-SMases)被认为是介导应激诱导神经酰胺产生的主要候选酶,并且已从细菌、酵母和哺乳动物细胞中鉴定、表征和克隆出了N-SMase活性。尽管这些酶之间的同源性水平较低,但一些被认为参与金属结合和催化的关键残基是保守的。这导致了一种共同催化机制的提出,因此,这些酶被认为形成了一个扩展的N-SMases家族。尽管对细胞培养和各种组织中的N-SMase活性进行了大量研究,但直到最近,由于缺乏对特定N-SMase酶的分子鉴定,阻碍了对这些蛋白质的调节、生理和病理作用的具体深入了解。在这篇综述中,我们首次总结了关于N-SMase家族的当前知识,重点关注来自细菌、酵母和哺乳动物细胞的克隆成员。我们还简要考虑了N-SMase研究的主要未来方向,这有望对鞘脂介导的功能提供非常重要和具体的见解。