Article

A transient increase in the activity of Src-family kinases induced by cell detachment delays anoikis of intestinal epithelial cells.

Division of Molecular and Cellular Biology, Sunnybrook and Women's College Health Sciences Center, Department of Medical Biophysics, University of Toronto, 2075 Bayview Avenue, S Wing, Room S218, Toronto, ON, Canada M4N 3M5.
Oncogene (impact factor: 6.37). 04/2005; 24(10):1727-37. DOI:10.1038/sj.onc.1208379 pp.1727-37
Source: PubMed

ABSTRACT Detachment of epithelial cells from the basement membrane (BM) induces apoptosis, a phenomenon now widely known as anoikis. Studies in mammary and intestinal epithelial cells have shown that the loss of attachment to the BM rapidly triggers reversible proapoptotic events from which the cells can recover if they reattach within a certain period. Thus, cells seem to be transiently protected from the initial detachment-induced proapoptotic events. The molecular mechanisms underlying such transient protection against anoikis are unknown. In this paper, we present evidence indicating that detachment of intestinal epithelial cells triggers a transient, yet significant increase in the activity of the tyrosine kinases c-Src and c-Fyn, and that this activation of Src-family kinases (SFK) contributes to the transient protection against anoikis in these cells. The protective signals from SFK are mediated by the PI3K pathway, and caveolin-1. In addition, we show that the MEK1-ERK1/2 pathway acts in a synergistic manner with SFK to protect intestinal epithelial cells from anoikis.

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Keywords

activation
 
anoikis
 
attachment
 
basement membrane
 
BM
 
Detachment
 
initial detachment-induced proapoptotic events
 
intestinal epithelial cells
 
intestinal epithelial cells triggers
 
MEK1-ERK1/2 pathway acts
 
molecular mechanisms
 
PI3K pathway
 
protective signals
 
SFK
 
synergistic manner
 
transient
 
transient protection
 
transiently
 

Mariano Andres Loza-Coll