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Am J Physiol Renal Physiol 286: F58-F67, 2004. First published September 16, 2003; doi:10.1152/ajprenal.00037.2003
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Greater tolerance of renal medullary cells for a slow increase in osmolality is associated with enhanced expression of HSP70 and other osmoprotective genes

Qi Cai, Joan D. Ferraris, and Maurice B. Burg

Laboratory of Kidney and Electrolyte Metabolism, National Heart, Lung,and Blood Institute, National Institutes of Health, Bethesda, Maryland 20892-1603

Submitted 28 January 2003 ; accepted in final form 9 September 2003

In tests of osmotic tolerance of renal inner medullary cells in tissue culture, osmolality has usually been increased in a single step, whereas in vivo the increase occurs gradually over several hours. We previously found that more passage 2 mouse inner medullary epithelial (p2mIME) cells survive a linear increase in NaCl and urea from 640 to 1,640 mosmol/kgH2O over 20 h (which is similar to the change that may occur in vivo) than they do a step increase. The present studies examine accompanying differences in gene expression. Among mRNAs of genes known to be protective, tonicity-responsive enhancer binding protein and aldose reductase increase with a linear but decrease with a step increase; betaine transporter BGT1 decreases with a step but not a linear increase; heat shock protein 70.1 (HSP70.1) and HSP70.3 increase more with a linear than a step increase; and osmotic stress protein 94 and heme oxygenase-1 increase with a linear but decrease with a step increase. mRNAs for known urea-responsive proteins, GADD153 and Egr-1, increase with both a step and linear increase. A step increase in urea alone reduces mRNAs, similar to the combination of NaCl and urea, but a step increase in NaCl alone does not. HSP70 protein increases substantially with a linear rise in osmolality but does not change significantly with a step rise. We speculate that poorer survival of p2mIME cells with a step than with linear increase in NaCl and urea is accounted for, at least in part, by urea-induced suppression of protective genes, particularly HSP70.

osmotic stress; organic osmolyte; heat shock protein; mRNA abundance



Address for reprint requests and other correspondence: Q. Cai, National Institutes of Health, Bldg. 10, Rm. 6N319, Bethesda, MD 20892-1603 (E-mail: caiq{at}nhlbi.nih.gov).




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