AJP - Heart ADInstruments data acquisition for life science
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Heart Circ Physiol 287: H1957-H1966, 2004. First published July 8, 2004; doi:10.1152/ajpheart.00568.2004
0363-6135/04 $5.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
287/5/H1957    most recent
00568.2004v1
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 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 HighWire
Right arrow Citing Articles via Web of Science (3)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Schwartz, F.
Right arrow Articles by Gavras, H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Schwartz, F.
Right arrow Articles by Gavras, H.

Novel targets of ANG II regulation in mouse heart identified by serial analysis of gene expression

Faina Schwartz,2 Arvi Duka,1 Irena Duka,1 Jing Cui,1 and Haralambos Gavras1

1Department of Medicine, Hypertension and Atherosclerosis Section and 2Genetics Program, Boston University School of Medicine, Boston, Massachusetts 02118

Submitted 10 June 2004 ; accepted in final form 1 July 2004

Although the central role of ANG II in cardiovascular homeostasis is well appreciated, the molecular circuitry of its many actions is not completely understood. With the use of serial analysis of gene expression to assess global transcriptional changes in the heart of mice after continuous 7-day ANG II administration, we identified patterns of gene expression indicative of cardiac remodeling, including coordinate regulation of genes previously described in a context of processes associated with hypertrophy and fibrosis. In addition, we discovered several novel ANG II targets, including characterized genes of known function, recently annotated genes of unknown function, and the putative genes not yet present in current databases. The serial analysis of gene expression approach to assess the role of ANG II presented in this report provides new venues for inquiries into ANG II-mediated cardiac function.

genome-wide transcriptional profiling; hypertension; cardiac remodeling; hypertrophy; fibrosis



Address for reprint requests and other correspondence: F. Schwartz, Dept. of Medicine, Genetics Program, Boston Univ. School of Medicine, 715 Albany St., L-320, Boston, MA 02118 (E-mail: fschw{at}bu.edu)




This article has been cited by other articles:


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
V. S. Kasi, H. D. Xiao, L. L. Shang, S. Iravanian, J. Langberg, E. A. Witham, Z. Jiao, C. J. Gallego, K. E. Bernstein, and S. C. Dudley Jr.
Cardiac-restricted angiotensin-converting enzyme overexpression causes conduction defects and connexin dysregulation
Am J Physiol Heart Circ Physiol, July 1, 2007; 293(1): H182 - H192.
[Abstract] [Full Text] [PDF]


Home page
Journal of Renin-Angiotensin-Aldosterone SystemHome page
W. M Maharsy, L. N Kadi, N. G Issa, K. M Bitar, A. H Der-Boghossian, R. Abrahamian, and A. B Bikhazi
Cross-talk related to insulin and angiotensin II binding on myocardial remodelling in diabetic rat hearts
Journal of Renin-Angiotensin-Aldosterone System, June 1, 2007; 8(2): 59 - 65.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2004 by the American Physiological Society.