Am. J. Respir. Cell Mol. Biol., Vol 15, No. 5, Nov 1996, 664-672.
Differential regulation of airway epithelial integrins by growth factors
A Wang, Y Yokosaki, R Ferrando, J Balmes and D Sheppard
Department of Medicine, San Francisco General Hospital, California, USA.
The pattern of integrin expression on human airway epithelium changes
significantly in injury or inflammation. In particular, two integrins, the
fibronectin receptor, alpha 5 beta 1 and the fibronectin/tenascin receptor
alpha v beta 6, are expressed at low or undetectable levels in normal
airways in vivo but are induced in response to airway epithelial injury. We
investigated the effects of various growth factors known to be present in
the airways on the expression of constitutively expressed and inducible
airway epithelial integrins using flow cytometry. In primary cultures of
human airway epithelial cells, transforming growth factor-beta 1 (TGF beta
1) dramatically increased expression of alpha v beta 6 and essentially did
not affect the expression of any other integrin, including alpha 5 beta 1.
In contrast, epidermal growth factor (EGF) upregulated surface levels of
both alpha v beta 6 and alpha 5 beta 1. Together, TGF beta 1 and EGF had an
additive effect on alpha v beta 6 and alpha 5 beta 1 expression while
increasing levels of alpha 2 beta 1 and decreasing expression of alpha 3
beta 1- and alpha 6- containing integrins. In contrast, the transformed
airway epithelial cell line, BEAS-2B, expressed a markedly different
repertoire of integrins. Integrin expression on BEAS-2B cells was not
affected by any of the growth factors tested in this study. These results
demonstrate that, in primary cultures of human airway epithelial cells, the
pattern of integrin expression can be dramatically altered by growth
factors. The inducible integrins, alpha v beta 6, and alpha 5 beta 1 are
most subject to regulation by growth factors and expression of each of
these can be differentially regulated. The differential regulation of the
two principal fibronectin receptors on airway epithelial cells suggests
that they may mediate different cellular responses to fibronectin.
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[Abstract]
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[Abstract]
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31930 - 31937.
[Abstract]
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H. Takahashi, T. Isobe, S. Horibe, J. Takagi, Y. Yokosaki, D. Sheppard, and Y. Saito
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J. Biol. Chem.,
July 28, 2000;
275(31):
23589 - 23595.
[Abstract]
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T. Tarui, A. P. Mazar, D. B. Cines, and Y. Takada
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[Abstract]
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Copyright © 1996 American Thoracic Society.
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