Access count of this item: 291
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
journal.pone.0035519.pdf | 526.97 kB | Adobe PDF | View/Open |
Title: | Role of Dlg5/lp-dlg, a Membrane-Associated Guanylate Kinase Family Protein, in Epithelial-Mesenchymal Transition in LLc-PK1 Renal Epithelial Cells. |
Authors: | Sezaki, Takuhito Inada, Kohki Sogabe, Takayuki Kakuda, Kumiyo Tomiyama, Lucia Matsuno, Yohsuke Ichikawa, Takafumi ![]() ![]() ![]() Matsuo, Michinori Ueda, Kazumitsu ![]() ![]() ![]() Kioka, Noriyuki ![]() ![]() ![]() |
Author's alias: | 木岡, 紀幸 |
Issue Date: | 23-Apr-2012 |
Publisher: | Public Library of Science |
Journal title: | PloS one |
Volume: | 7 |
Issue: | 4 |
Thesis number: | e35519 |
Abstract: | Discs large homolog 5 (Dlg5) is a member of the membrane-associated guanylate kinase adaptor family of proteins, some of which are involved in the regulation of epithelial-to-mesenchymal transition (EMT). Dlg5 has been described as a susceptibility gene for Crohn's disease; however, the physiological function of Dlg5 is unknown. We show here that transforming growth factor-β (TGF-β)-induced EMT suppresses Dlg5 expression in LLc-PK1 cells. Depletion of Dlg5 expression by knockdown promoted the expression of the mesenchymal marker proteins, fibronectin and α-smooth muscle actin, and suppressed the expression of E-cadherin. In addition, activation of JNK and p38, which are stimulated by TGF-β, was enhanced by Dlg5 depletion. Furthermore, inhibition of the TGF-β receptor suppressed the effects of Dlg5 depletion. These observations suggest that Dlg5 is involved in the regulation of TGF-βreceptor-dependent signals and EMT. |
Rights: | © 2012 Sezaki et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
URI: | http://hdl.handle.net/2433/155466 |
DOI(Published Version): | 10.1371/journal.pone.0035519 |
PubMed ID: | 22539977 |
Appears in Collections: | Journal Articles |

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.