Heat shock protein 72, a chaperone abundant in renal papilla, counteracts urea-mediated inhibition of enzymes

• Published in: Pflügers Archiv Vol. 445; no. 1; pp. 67 - 73
• Main Authors: Neuhofer, Wolfgang, Fraek, Maria-Luisa, X Beck, Franz
• Format: Journal Article
• Language: English
• Published: Germany Springer Nature B.V 01.10.2002
• Subjects: Animals; beta-Galactosidase - metabolism; Heat shock proteins; Heat-Shock Proteins - pharmacology; Heat-Shock Proteins - physiology; HSP72 Heat-Shock Proteins; Kidney Medulla - metabolism; Kidneys; L-Lactate Dehydrogenase - metabolism; Male; Molecular Chaperones - pharmacology; Molecular Chaperones - physiology; Osmolar Concentration; Proteins; Rats; Rats, Wistar; Recombinant Proteins - pharmacology; Urea - metabolism; Urea - pharmacology
• ISSN: 0031-6768; 1432-2013
• DOI: 10.1007/s00424-002-0858-1

Urea, at concentrations routinely observed in the renal inner medulla during antidiuresis in many mammals, is a potent protein destabilizing agent that reduces the activity of many enzymes. The molecular chaperone heat shock protein 72 (HSP72) is expressed at about 5 ng/ micro g protein in the renal papilla and is thus 40 times more abundant than in the isosmotic cortex and may counteract the deleterious effects of high urea concentrations in the inner medulla. To test this hypothesis, we examined the effect of recombinant HSP72 on lactate dehydrogenase activity in the presence of 0.8 M urea in a cell-free system. The urea-induced increase in K(m) was reduced by 85% in the presence of 1 microM HSP72 but only by 6% by 100 mM betaine, a "counteracting" trimethylamine osmolyte. Conversely, the decrease in V(max) with 0.8 M urea was not affected by HSP72 but was attenuated by 42% in the presence of betaine. The protective effect of HSP72 was confirmed by the attenuation of the urea-induced decrease in the activity of another model enzyme, beta-galactosidase, by lysate of HSP72-overexpressing MDCK cells. Hence, in addition to the trimethylamine osmolytes, HSP72 may participate in counteracting urea-mediated effects on protein function in the renal papilla.