Skip Navigation

Cardiovascular Research 2001 50(1):115-124; doi:10.1016/S0008-6363(01)00198-5
© 2001 by European Society of Cardiology
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow E-letters: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when E-letters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Hammerer-Lercher, A.
Right arrow Articles by Dirnhofer, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hammerer-Lercher, A.
Right arrow Articles by Dirnhofer, S.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Copyright © 2001, European Society of Cardiology

Hypoxia induces heat shock protein expression in human coronary artery bypass grafts

Angelika Hammerer-Lerchera,*, Johannes Mairb, Johannes Bonattic, Stefan B.C. Watzkac, Bernd Puschendorfa and Stephan Dirnhoferd

aDepartment of Med. Chemistry and Biochemistry, Division of Clinical Biochemistry, University of Innsbruck, Fritz-Pregl-Strasse 3, A-6020 Innsbruck, Austria
bDepartment of Cardiology, University of Innsbruck, Innsbruck, Austria
cDepartment of Cardiac Surgery, University of Innsbruck, Innsbruck, Austria
dDepartment of Pathology, University of Innsbruck, Innsbruck, Austria

* Corresponding author. Tel.: +43-512-507-3522; fax: +43-512-507-2876 angelika.lercher{at}uibk.ac.at

Objective: Heat shock proteins (HSPs) are molecular chaperones which are essential for cell survival. Heat shock and hypoxia markedly increase the expression of several HSPs in various tissues, i.e. heart. In our in vitro study, we investigated whether HSPs are inducible in human vessels which are used as coronary artery bypass grafts. Methods: We used remnants of the saphenous vein and the internal mammary artery from 34 patients undergoing coronary artery bypass surgery. Each vessel was divided into segments, one for control conditions at 37°C (5% CO2–95% air), the remaining ones for thermal (30 min at 42°C) or hypoxic treatment (6 h oxygen deprivation with nitrogen). The expression of Hsp60, Hsp72 and Hsp73 was investigated by immunohistochemistry and Western-blot analysis. Results: Compared to controls, segments of the saphenous vein undergoing heat treatment showed significantly increased expression of Hsp72 in the intima (P = 0.035) and Hsp73 in the media (P = 0.003). In the internal mammary artery, Hsp72 and Hsp73 were expressed in the intima at significantly higher levels (P = 0.042 each). A 6 h oxygen deprivation with nitrogen resulted in elevated levels of Hsp60 (media: P = 0.048), of Hsp72 (intima: P<0.001 and media: P = 0.004) and of Hsp73 (intima: P = 0.029) in the saphenous vein. In the internal mammary artery, Hsp73 expression was significantly enhanced (intima: P = 0.048 and media: P = 0.017). The results were confirmed by Western-blot analysis in representative veins. Conclusions: These findings demonstrate the common cellular defense mechanism of HSP expression in response to stress in coronary artery bypass grafts. Hypoxia and heat treatment strongly induce Hsp72 and Hsp73 expression in human coronary artery bypass grafts.

KEYWORDS Arteries; Cardiovascular surgery; Hypoxia/anoxia; Preconditioning; Veins


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.