共 85 条
The tail of integrin activation
被引:133
作者:

Anthis, Nicholas J.
论文数: 0 引用数: 0
h-index: 0
机构:
NIDDK, Chem Phys Lab, NIH, Bethesda, MD 20892 USA Univ Oxford, Dept Biochem, Oxford OX1 3DR, England

Campbell, Iain D.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Oxford, Dept Biochem, Oxford OX1 3DR, England Univ Oxford, Dept Biochem, Oxford OX1 3DR, England
机构:
[1] Univ Oxford, Dept Biochem, Oxford OX1 3DR, England
[2] NIDDK, Chem Phys Lab, NIH, Bethesda, MD 20892 USA
基金:
英国生物技术与生命科学研究理事会;
关键词:
BINDING-LIKE DOMAIN;
STRUCTURAL BASIS;
CYTOPLASMIC DOMAIN;
TALIN HEAD;
CRYSTAL-STRUCTURE;
FILAMIN BINDING;
TRANSMEMBRANE;
COMPLEX;
PHOSPHORYLATION;
ADHESION;
D O I:
10.1016/j.tibs.2010.11.002
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:
Integrins are essential adhesion receptors found on the surfaces of all metazoan cells. As regulators of cell migration and extracellular matrix assembly, these membrane-spanning heterodimers are critical for embryonic development, tissue repair and immune responses. Signals transmitted by integrins from outside to inside the cell promote cell survival and proliferation, but integrin affinity for extracellular ligands can also be controlled by intracellular cues. This bidirectional signaling is mediated by the short cytoplasmic tails of the two integrin subunits. Recent structural and functional studies of various integrin fragments and complexes between the cytoplasmic tails and intracellular proteins, such as talin, have provided new insight into the signaling processes centered around the tails, particularly inside-out integrin activation.
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收藏
页码:191 / 198
页数:8
相关论文
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