期刊
DEVELOPMENTAL CELL
卷 22, 期 1, 页码 116-130出版社
CELL PRESS
DOI: 10.1016/j.devcel.2011.10.030
关键词
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资金
- National Institutes of Health (NIH) [CA104708, GM057549, P30-CA-014520]
- American Heart Association [10POST4290052]
Polarized delivery of signaling and adhesion molecules to the leading edge is required for directional migration of cells. Here, we describe a role for the PIP(2)-synthesizing enzyme, PIPKI gamma i2, in regulation of exocyst complex control of cell polarity and polarized integrin trafficking during migration. Loss of PIPKI gamma i2 impaired directional migration, formation of cell polarity, and integrin trafficking to the leading edge. Upon initiation of directional migration, PIPKI gamma i2 via PIP(2) generation controls the integration of the exocyst complex into an integrin-containing trafficking compartment that requires the talin-binding ability of PIPKI gamma i2, and talin for integrin recruitment to the leading edge. A PIP2 requirement is further emphasized by inhibition of PIPKI gamma i2-regulated directional migration by an Exo70 mutant deficient in PIP2 binding. These results reveal how phosphoinositide generation orchestrates polarized trafficking of integrin in coordination with talin that links integrins to the actin cytoskeleton, processes that are required for directional migration.
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