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PMID: 10027073 Published · ppublish English Journal Article Review

Signalling and gene regulation by urea and NaCl in the renal medulla.

Clinical and experimental pharmacology & physiology ·Vol. 26 ·No. 1 ·1999-01-00 ·Pages 69-73

Cohen DM

Abstract

1. Cells of the mammalian renal medulla are routinely subjected to an enormously elevated and labile ambient osmolality as a consequence of the renal concentrating mechanism. The present review focuses on the most recent advances in hyperosmotic solute-mediated signal transduction and regulation of gene transcription in cells of the kidney medulla. 2. On the basis of osmolality alone, NaCl and urea are the principal renal medullary solutes. 3. Urea, which is membrane permeant, activates transcription of immediate-early genes via an extracellular signal-regulated kinase (ERK)/Elk-1-dependent pathway. Urea also activates multiple effectors characteristic of a receptor tyrosine kinase-like signalling cascade. 4. In contrast, the functionally impermeant solute NaCl activates transcription of tonicity responsive genes (principally genes encoding proteins essential for osmolyte uptake or synthesis) via a unique consensus element contained within their 5' flanking sequences. 5. An activity exhibiting tonicity inducible sequence-specific interaction with this DNA element has been identified. 6. Hypertonicity, like thermal stress, activates transcription of genes encoding heat shock proteins. The relationship between signalling events leading to tonicity mediated and heat shock-mediated gene transcription remains to be established.

MeSH Terms
Animals Calcium-Calmodulin-Dependent Protein Kinases/physiology Gene Expression Regulation/drug effects,physiology Kidney Medulla/drug effects,physiology Osmolar Concentration Signal Transduction/drug effects,genetics Sodium Chloride/pharmacology Urea/pharmacology
Chemicals
Sodium Chloride Urea Calcium-Calmodulin-Dependent Protein Kinases
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Cohen D M
Division of Nephrology, Oregon Health Sciences University, Portland, USA. cohend@ohsu.edu
Article Info
Journal
Clinical and experimental pharmacology & physiology
Abbr.
Clin Exp Pharmacol Physiol
ISSN
0305-1870
Published
1999-01-00
Pages
69-73
Language
English
Region
Australia
NLM ID
0425076
Subset
IM
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