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


     


Physiol. Genomics (October 23, 2007). doi:10.1152/physiolgenomics.00201.2007
This Article
Right arrow Full Text (PDF)
Right arrow Supplemental Figures and Tables
Right arrow All Versions of this Article:
32/2/229    most recent
00201.2007v1
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 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 Uawithya, P.
Right arrow Articles by Knepper, M. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Uawithya, P.
Right arrow Articles by Knepper, M. A.
Submitted on August 28, 2007
Accepted on October 17, 2007

Transcriptional Profiling of Native Inner Medullary Collecting Duct Cells from Rat Kidney

Panapat Uawithya1, Trairak Pisitkun1, Brian E. Ruttenberg1, and Mark A. Knepper1*

1 NHLBI, NIH, Bethesda, Maryland, United States

* To whom correspondence should be addressed. E-mail: knep{at}helix.nih.gov.

Vasopressin acts on the inner medullary collecting duct (IMCD) in the kidney to regulate water and urea transport. To obtain a ‘parts list’ of gene products expressed in the IMCD, we carried out mRNA profiling of freshly isolated rat IMCD cells using Affymetrix Rat 230 2.0 microarrays with approximately 31,000 features. 7913 annotated transcripts were found to be expressed above background in the IMCD cells. We have created an online database (the "IMCD Transcriptome Database" ) to make the results publicly accessible. Among the 30 transcripts with the greatest signals on the arrays were three water channels: aquaporin-2, aquaporin-3, and aquaporin-4, all of which have been reported to be targets for regulation by vasopressin. In addition, the transcript with the greatest signal among members of the solute carrier (SLC) family of genes was the UT-A urea transporter (Slc14a2), which is also regulated by vasopressin. The V2 vasopressin receptor was strongly expressed, but the V1a and V1b vasopressin receptors did not produce signals above background. Among the 200 protein kinases expressed, the serum-glucocorticoid regulated kinase (Sgk1) had the greatest signal intensity in the IMCD. WNK1 and WNK4 were also expressed in the IMCD with a relatively high signal intensity as was protein kinase A ({beta}-catalytic subunit). In addition, a large number of transcripts corresponding to AKAPs and 14-3-3 proteins (phospho-S/T binding proteins) were expressed. Altogether, the results combine with proteomics studies of the IMCD to provide a framework for modeling complex interaction networks responsible for vasopressin action in collecting duct cells.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Visit Other APS Journals Online
Copyright © 2007 by the American Physiological Society.