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体外和体内哺乳动物鞘氨醇-1-磷酸磷酸水解酶活性的测定。

Measurement of mammalian sphingosine-1-phosphate phosphohydrolase activity in vitro and in vivo.

作者信息

Maceyka Michael, Milstien Sheldon, Spiegel Sarah

机构信息

Department of Biochemistry and Molecular Biology, Virginia Commonwealth University School of Medicine, Richmond, Virginia, USA.

出版信息

Methods Enzymol. 2007;434:243-56. doi: 10.1016/S0076-6879(07)34013-5.

Abstract

Sphingolipid metabolites have emerged as key players in diverse processes including cell migration, growth, and apoptosis. Ceramide and sphingosine typically inhibit cell growth and induce apoptosis, while sphingosine-1-phosphate (S1P) promotes cell growth, inhibits apoptosis, and induces cell migration. Thus, enzymes that regulate the levels of these sphingolipid metabolites are of critical importance to understanding cell fate. There are two known mammalian isoforms of S1P phosphohydrolases (SPP1 and SPP2) that reversibly degrade S1P to sphingosine. This chapter discusses the importance of SPPs and describes assays that can be used to measure the activity of these two specific S1P phosphohydrolases in cells and cell lysates.

摘要

鞘脂代谢产物已成为多种细胞进程中的关键参与者,这些进程包括细胞迁移、生长和凋亡。神经酰胺和鞘氨醇通常会抑制细胞生长并诱导凋亡,而1-磷酸鞘氨醇(S1P)则促进细胞生长、抑制凋亡并诱导细胞迁移。因此,调节这些鞘脂代谢产物水平的酶对于理解细胞命运至关重要。已知有两种哺乳动物的S1P磷酸水解酶同工型(SPP1和SPP2),它们可将S1P可逆地降解为鞘氨醇。本章将讨论SPP的重要性,并描述可用于测量细胞和细胞裂解物中这两种特定S1P磷酸水解酶活性的检测方法。

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