Erratum: Integrins in regulation of tissue development and function. J Pathol; 200: 471–480

Authors

  • Erik HJ Danen,

    Corresponding author
    1. Division of Cell Biology, The Netherlands Cancer Institute, Amsterdam, The Netherlands
    • Division of Cell Biology, The Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands.
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  • Arnoud Sonnenberg

    Corresponding author
    1. Division of Cell Biology, The Netherlands Cancer Institute, Amsterdam, The Netherlands
    • Division of Cell Biology, The Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands.
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Abstract

The original article to which this Erratum refers was published in Journal of Pathology; 200(4): 471–480.

It has been brought to the attention of the publishers that there were errors on pages 476, 477 and 480 of the orginally published manuscript. These errors have now been rectified, and to facilitate greater legibility for our readers, the corrected article has been reproduced in its entirety.

Cell adhesion is indispensable for embryonic development and for proper tissue function. In metazoans, integrins are the major adhesion receptors that connect cells to components of the extracellular matrix. Integrins are implicated in assembly of extracellular matrices, cell adhesion and migration on extracellular matrices, and in vertebrates (in which the integrin family has expanded) they can also mediate cell–cell adhesion. Furthermore, integrin-mediated adhesion can modulate many different signal transduction cascades and support cell survival, proliferation, and influence the expression of differentiation-related genes. In this review we briefly explain how integrins can affect so many different aspects of cell behavior and discuss evidence for roles of integrins in tissue development, function, and disease. Copyright © 2003 John Wiley & Sons, Ltd.

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