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First published online June 23, 2005


Journal of Cell Science 118, 1302e (2005)
© The Company of Biologists Limited
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In this issue

Peri-implantation at a PINCH


During the development of multicellular organisms, integrins act through integrin-associated molecules to regulate essential aspects of cell-cell and cell-matrix adhesion, cell polarity and cell survival. On p. 2913, Reinhard Fässler and co-authors report that the integrin-associated protein PINCH1 regulates all four of these processes during the peri-implantation stage of mouse development. PINCH1 interacts with integrin cytoplasmic tails at focal adhesions via integrin-linked kinase (ILK). The authors show that, like ß1-integrin- and Ilk-deficient mice, mouse embryos carrying a disrupted PINCH1 gene arrest at the peri-implantation stage. To pinpoint this phenotype, the authors examined embryoid bodies (EBs), an experimental model for this stage of development. Although PINCH1-null EBs show many of the same defects as ß1-integrin- and Ilk-mutant EBs (including abnormal epiblast polarity and detachment of cells from matrix), they also exhibit abnormal cell-cell adhesion and increased endodermal apoptosis. Thus, the authors conclude, PINCH1 acts in both an ILK-dependent and an ILK-independent manner during mouse peri-implantation.


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Related articles in JCS:

PINCH1 regulates cell-matrix and cell-cell adhesions, cell polarity and cell survival during the peri-implantation stage
Shaohua Li, Randi Bordoy, Fabio Stanchi, Markus Moser, Attila Braun, Oliver Kudlacek, Ulla M. Wewer, Peter D. Yurchenco, and Reinhard Fässler
JCS 2005 118: 2913-2921. [Abstract] [Full Text]  




This Article
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