Cytoskeleton-membrane interactions in membrane raft structure

被引:189
作者
Chichili, Gurunadh R. [1 ]
Rodgers, William [1 ]
机构
[1] Oklahoma Med Res Fdn, Cardiovasc Biol Res Program, Oklahoma City, OK 73104 USA
关键词
Membrane rafts; Actin cytoskeleton; Phosphatidylinositol; 4; 5; bisphosphate; T cell signaling; Src family kinases; T-CELL-ACTIVATION; PROTEIN-TYROSINE KINASE; GPI-ANCHORED PROTEINS; SINGLE-MOLECULE TRACKING; PLECKSTRIN HOMOLOGY DOMAINS; LIPID RAFTS; PLASMA-MEMBRANE; IMMUNOLOGICAL SYNAPSE; ACTIN CYTOSKELETON; PHOSPHATIDYLINOSITOL 4,5-BISPHOSPHATE;
D O I
10.1007/s00018-009-0022-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cell membranes are structurally heterogeneous, composed of discrete domains with unique physical and biological properties. Membrane domains can form through a number of mechanisms involving lipid-lipid and protein-lipid interactions. One type of membrane domain is the cholesterol-dependent membrane raft. How rafts form remains a current topic in membrane biology. We review here evidence of structuring of rafts by the cortical actin cytoskeleton. This includes evidence that the actin cytoskeleton associates with rafts, and that many of the structural and functional properties of rafts require an intact actin cytoskeleton. We discuss the mechanisms of the actin-dependent raft organization, and the properties of the actin cytoskeleton in regulating raft-associated signaling events. We end with a discussion of membrane rafts and the actin cytoskeleton in T cell activation, which function synergistically to initiate the adaptive immune response.
引用
收藏
页码:2319 / 2328
页数:10
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