Donate Help Contact The AHA Sign In Home
American Heart Association
Hypertension
Search: search_blue_button Advanced Search
Hypertension. 2001;38:153

This Article
Right arrow Full Text
Right arrow Alert me when this article is cited
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 Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Monti, J.
Right arrow Articles by Hübner, N.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Monti, J.
Right arrow Articles by Hübner, N.

(Hypertension. 2001;38:153-a.)
© 2001 American Heart Association, Inc.


Hypertension Electronic Pages

Expression Analysis Using Oligonucleotide Microarrays in Mice Lacking Bradykinin Type 2 Receptors

Jan Monti; Volkmar Gross; Friedrich C. Luft; Anna Franca Milia; Herbert Schulz; Rainer Dietz; Arya M. Sharma; Norbert Hübner
Abstract

Abstract— We recently conducted detailed cardiovascular and blood pressure-related phenotypic studies of mice lacking the bradykinin-B2 receptor and were unable to identify a phenotype despite insensitivity to infused bradykinin. We therefore used oligonucleotide microarray analysis of some 12 000 genes and expressed sequence tags to identify molecular mechanisms that might be involved in compensating for the lack of a functional B2 receptor in the kidneys of the mice. We identified 2 gene families that may have an impact on cardiovascular regulation and the bradykinin pathway. A water transport channel in the kidney, AQP4, was downregulated in the mice, whereas other members of the gene family did not show differences in expression levels. In addition, a number of serine proteases were upregulated in B2 receptor-deficient mice. These genes are all located within a gene cluster on mouse chromosome 7. The findings were verified by an independent method. We suggest that microarray analysis has usefulness in elucidating otherwise unappreciated compensatory signaling pathways.


Key Words: bradykinin • genes • chromosome 7 • microarray analysis