Worgall Tilla S
Department of Pathology, Columbia University, 168 W 168 St, BB 457, New York, NY 10032, USA.
Subcell Biochem. 2008;49:371-85. doi: 10.1007/978-1-4020-8830-8_14.
Sphingolipids, together with phospholipids and cholesterol are key components of membrane lipid bilayers, contribute to specialized membrane domains called rafts and function as signaling molecules. Sphingolipids have been recognized to exert a distinct role in the post-transcriptional regulation of the sterol-regulatory element binding proteins (SREBPs), key transcription factors of lipid synthesis. Sphingolipid synthesis is an obligate activator of SREBP. Inhibition of sphingolipid synthesis decreases SREBP on a post-transcriptional level. With the exception of enzymes that synthesize sphingolipids, SREBPs regulate the transcription of key enzymes that synthesize cholesterol, phospholipids and fatty acids. This observation suggests an exclusive role for sphingolipids in the regulation of lipid metabolism. Although exact mechanisms how sphingolipids regulate lipid metabolism are currently not known, this relationship has important implications with regard to cellular lipid homeostasis, composition of lipoproteins and development of atherosclerosis.
鞘脂与磷脂和胆固醇一起,是膜脂双层的关键成分,有助于形成称为脂筏的特殊膜结构域,并作为信号分子发挥作用。鞘脂已被认为在固醇调节元件结合蛋白(SREBPs)的转录后调节中发挥独特作用,SREBPs是脂质合成的关键转录因子。鞘脂合成是SREBP的必需激活剂。抑制鞘脂合成会在转录后水平降低SREBP。除了合成鞘脂的酶外,SREBPs还调节合成胆固醇、磷脂和脂肪酸的关键酶的转录。这一观察结果表明鞘脂在脂质代谢调节中具有独特作用。尽管目前尚不清楚鞘脂如何调节脂质代谢的确切机制,但这种关系在细胞脂质稳态、脂蛋白组成和动脉粥样硬化发展方面具有重要意义。