Lipid raft: A floating island of death or survival

被引:168
作者
George, Kimberly S. [1 ,2 ,3 ]
Wu, Shiyong [1 ,2 ]
机构
[1] Ohio Univ, Edison Biotechnol Inst, Athens, OH 45701 USA
[2] Ohio Univ, Dept Chem & Biochem, Athens, OH 45701 USA
[3] Marietta Coll, Dept Chem, Marietta, OH 45750 USA
关键词
Lipid raft; Cholesterol; Death receptor; Kinase; Calcium channel; Apoptosis; DOWNSTREAM SIGNALING MOLECULES; CELL-SURFACE-ANTIGEN; PROTEIN-KINASE; TRITERPENOID SAPONINS; INDUCED ACTIVATION; FAS AGGREGATION; JNK ACTIVATION; MEMBRANE RAFTS; IN-VIVO; C-JUN;
D O I
10.1016/j.taap.2012.01.007
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Lipid rafts are microdomains of the plasma membrane enriched in cholesterol and sphingolipids, and play an important role in the initiation of many pharmacological agent-induced signaling pathways and toxicological effects. The structure of lipid rafts is dynamic, resulting in an ever-changing content of both lipids and proteins. Cholesterol, as a major component of lipid rafts, is critical for the formation and configuration of lipid raft microdomains, which provide signaling platforms capable of activating both pro-apoptotic and antiapoptotic signaling pathways. A change of cholesterol level can result in lipid raft disruption and activate or deactivate raft-associated proteins, such as death receptor proteins, protein kinases, and calcium channels. Several anti-cancer drugs are able to suppress growth and induce apoptosis of tumor cells through alteration of lipid raft contents via disrupting lipid raft integrity. Published by Elsevier Inc.
引用
收藏
页码:311 / 319
页数:9
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