Physiol. Genomics Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Physiol. Genomics 8: 107-114, 2002; doi:10.1152/physiolgenomics.00039.2001
1094-8341/02 $5.00
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 HighWire
Right arrow Citing Articles via ISI Web of Science (4)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ten Hagen, K. G.
Right arrow Articles by Melvin, J. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ten Hagen, K. G.
Right arrow Articles by Melvin, J. E.
Received 22 May 2001; accepted in final form 13 December 2001.
Physiological Genomics 8:107-114 (2002)
1094-8341/02 $5.00 © 2002 American Physiological Society

Analysis of isoproterenol-induced changes in parotid gland gene expression

Kelly G. Ten Hagen, Marlene M. Balys, Lawrence A. Tabak and James E. Melvin

Center for Oral Biology, Aab Institute for Biomedical Sciences, University of Rochester, Rochester, New York 14642

Parotid gland acinar cells undergo marked hypertrophy and hyperplasia upon systemic exposure to the ß-adrenergic agonist, isoproterenol. This glandular enlargement is accompanied by substantial cellular changes including DNA synthesis, an increase in glandular protein synthesis, and differential changes in RNA transcription. To gain a more detailed understanding of the underlying changes induced by isoproterenol, we have examined the parotid gland gene expression profile of mice up to 24 h post-isoproterenol injection using high-density oligonucleotide arrays. Depending upon the exposure time, between 22 and 48 of the ~6,500 mouse genes and expressed sequence tags (ESTs) analyzed displayed significant changes in expression patterns. Genes that were previously shown to be repressed ({alpha}-amylase) or activated (proline-rich proteins) following isoproterenol exposure were found to be similarly affected in this experiment, validating this technique. This study demonstrates that the oligonucleotide array technology is a useful tool for examining isoproterenol-induced salivary gland gene expression changes. Using this as a starting point, we can begin to dissect the specific pathways involved in mediating isoproterenol action within the parotid gland.

high-density oligonucleotide arrays; proline-rich protein; ß-adrenergic agonist




This article has been cited by other articles:


Home page
J. Histochem. Cytochem.Home page
J.-F. Huaulme, Y. Courty, F. Rougeon, and I. Rosinski-Chupin
Androgen Regulation of SMR2 Gene Expression in Rat Submandibular Gland: Evidence for a Graded but not a Binary Response
J. Histochem. Cytochem., October 1, 2003; 51(10): 1317 - 1329.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online