Journal
CELL CYCLE
Volume 7, Issue 4, Pages 444-448Publisher
TAYLOR & FRANCIS INC
DOI: 10.4161/cc.7.4.5452
Keywords
Abl; tyrosine kinases; cadherin; cell-cell adhesion; Rac; Rho; Crk; adherens junctions
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Funding
- NCI NIH HHS [R01 CA070940-12, R01 CA070940, CA70940] Funding Source: Medline
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Formation and dissolution of intercellular adhesions are processes of paramount importance during tissue morphogenesis and for pathological conditions such as tumor metastasis. Cadherin-mediated intercellular adhesion requires dynamic regulation of the actin cytoskeleton. The pathways that link cadherin signaling to cytoskeletal regulation remain poorly defined. We have recently uncovered a novel role for the Abl family of tyrosine kinases linking cadherin-mediated adhesion to actin dynamics via the regulation of Rho family GTPases. Abl kinases are activated by cadherin engagement, localize to cell-cell junctions and are required for the formation of adherens junctions. Notably, we showed that Abl kinases are required for Rac activation during formation of adherens junctions, and also regulate a Rho-ROCK-myosin signaling pathway that is required for the maintenance of intercellular adhesion. Here we show that Abl kinases regulate the formation and strengthening of adherens junctions downstream of active Rac, and that Abl tyrosine kinases are components of a positive feed-back loop that employs the Crk/CrkL adaptor proteins to promote the formation and maturation of adherens junctions.
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