Rho activation is required for transforming growth factor-beta-induced epithelial-mesenchymal transition in lens epithelial cells
- Authors
- Cho, Hee Jun; Yoo, Jiyun
- Issue Date
- Oct-2007
- Publisher
- ACADEMIC PRESS LTD ELSEVIER SCIENCE LTD
- Keywords
- transforming growth factor-beta; epithelial-mesenchymal transition; Smad; Rho; ROCK
- Citation
- CELL BIOLOGY INTERNATIONAL, v.31, no.10, pp 1225 - 1230
- Pages
- 6
- Indexed
- SCIE
SCOPUS
- Journal Title
- CELL BIOLOGY INTERNATIONAL
- Volume
- 31
- Number
- 10
- Start Page
- 1225
- End Page
- 1230
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/28278
- DOI
- 10.1016/j.cellbi.2007.04.006
- ISSN
- 1065-6995
1095-8355
- Abstract
- Lens epithelial cells undergo epithelial-mesenchymal transition (EMT) after injury as in cataract extraction, leading to fibrosis of the lens capsule. We have recently shown that TGF-beta-induced EMT in lens epithelial cells depends on PI3 kinase/Akt signal pathway. In this report, we suggest Smad3 is necessary for TGF-beta-induced EMT by showing that the expression of dominant-negative Smad3 blocks the expression of a-smooth muscle actin (alpha-SMA) and morphological changes. We also show that TGF-induces a biphasic change in Rho activity, and that Y27632, a selective inhibitor of Rho effector ROCK, inhibits TGF-beta-induced EMT in vitro and in vivo. We finally show that Smad3 activation and Rho signal activation is independent each other. All of these findings suggest that Rho/ROCK activation together with Smad3 is necessary for TGF-beta-induced EMT in lens epitheliat cells. (c) 2007 International Federation for Cell Biology. (c) Published by Elsevier Ltd. All rights reserved.
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