ERJ
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Published online before print June 27, 2007, 10.1183/09031936.00141805
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Gawaziuk, J. P.
Right arrow Articles by Stephens, N. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Gawaziuk, J. P.
Right arrow Articles by Stephens, N. L.
Eur Respir J 2007; 30:643-652
Copyright ©ERS Journals Ltd 2007

Transforming growth factor-ß as a differentiating factor for cultured smooth muscle cells

J. P. Gawaziuk, X. Ma, F. Sheikh, Z-Q. Cheng, P. A. Cattini and N. L. Stephens

Dept of Physiology, Faculty of Medicine, University of Manitoba, Winnipeg, MB, Canada.

CORRESPONDENCE: N. L. Stephens, Dept of Physiology, Faculty of Medicine, John Buhler Research Centre, Room 537, 715 McDermot Avenue, Winnipeg, MB R3E 3P4, Canada. Fax: 1 2047893941. E-mail: nstephe{at}ms.umanitoba.ca

Keywords: Decorin, double mass spectrometry, matrix metalloproteinase-2, SMAD2, transforming growth factor-ß1, transforming growth factor-ß-RII

Received: December 1, 2005
Accepted June 19, 2007

The aim of the present study was to determine whether the development of supercontractile smooth muscle cells, contributing to the nonspecific hyperreactivity of airways in asthmatic patients, is due to transforming growth factor (TGF)-ß.

In cultured smooth muscle cells starved by removal of 10% foetal bovine serum for 7 days, growth arrest was seen; 30% became elongated and demonstrated super contractility. Study of conditioned medium suggested that the differentiating factor was TGF-ß. Sodium dodecyl sulphate–polyacrylamide gel electrophoresis (SDS–PAGE) was carried out on conditioned medium from the arrested cells. Two protein bands were identified as matrix metalloproteinase (MMP)-2 and TGF-ß1. To determine second messenger signalling by SMAD2, Western blotting and confocal microscopy were employed.

Conditioned medium from arrested cultures showed the presence of MMP-2 and TGF-ß1, as revealed by SDS–PAGE; 68- and 25-kDa bands were seen. Differentiation was confirmed by upregulation of marker proteins, smooth muscle type myosin heavy chain and myosin light chain kinase. Confirmation was obtained by downregulating these proteins with decorin treatment, which reduces the levels of active TGF-ß and an adenoviral dominant-negative vector coding for a mutated type II TGF-ß-receptor. Activation of second messenger signalling was demonstrated immunocytochemically by the presence of phosphorylated SMAD2 and SMAD4.

Transforming growth factor-ß is likely to be the differentiating factor responsible for the development of these supercontractile smooth muscle cells. The development of such cells in vivo after cessation of an asthmatic attack could contribute to the nonspecific hyperreactivity of airways seen in patients.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2007 by the European Respiratory Society.