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タイトル: Role of Dlg5/lp-dlg, a Membrane-Associated Guanylate Kinase Family Protein, in Epithelial-Mesenchymal Transition in LLc-PK1 Renal Epithelial Cells.
著者: Sezaki, Takuhito
Inada, Kohki
Sogabe, Takayuki
Kakuda, Kumiyo
Tomiyama, Lucia
Matsuno, Yohsuke
Ichikawa, Takafumi  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0002-0490-4176 (unconfirmed)
Matsuo, Michinori
Ueda, Kazumitsu  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0003-2980-6078 (unconfirmed)
Kioka, Noriyuki  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0002-2708-537X (unconfirmed)
著者名の別形: 木岡, 紀幸
発行日: 23-Apr-2012
出版者: Public Library of Science
誌名: PloS one
巻: 7
号: 4
論文番号: e35519
抄録: 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.
著作権等: © 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(出版社版): 10.1371/journal.pone.0035519
PubMed ID: 22539977
出現コレクション:学術雑誌掲載論文等

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