The osmolality of the blood in the renal inner medulla is high and varies with the urinary concentration. Both NaCl and urea are elevated. The medullary cells evidently survive and function in this adverse environment. The ongoing studies are concerned with understanding the mechanisms involved. When cells are stressed by a high salt environment, they generally accumulate osmotically active organic solutes (""""""""osmolytes"""""""") in order to maintain a favorable internal milieu, while regulating their volume. We identified the organic osmolytes in renal inner medullary cells as glycerophosphocholine (GPC), betaine, sorbitol, taurine, and inositol, and showed that the osmolyte levels varied with urine concentration (and, presumably, medullary salt and urea concentrations). We are now using renal cell cultures and living animals to study the mechanism and control of osmoregulatory accumulation of these organic osmolytes, including the transcription factor (TonEBP/OREBP) that is involved. High NaCl signals activation of TonEBP via PKA, ATM and other systems. In addition, the acute response to high osmolality may include cell cycle arrest and apoptosis in proliferating cultures of renal medullary cells. High NaCl causes DNA damage in cell culture, while high urea causes both DNA (8-oxoguanine lesions) and protein(cabonylation) damage. Both the DNA damage and protein carbonylation are present in normal renal inner medullas. The DNA damage is rapidly repaired in vivo when renal inner medullary osmolality is reduced by the diuretic, furosemide. We are studying the mechanisms involved, including the role of p53, p38, and GADD proteins.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Intramural Research (Z01)
Project #
1Z01HL001283-16
Application #
6817679
Study Section
(LKEM)
Project Start
Project End
Budget Start
Budget End
Support Year
16
Fiscal Year
2003
Total Cost
Indirect Cost
Name
U.S. National Heart Lung and Blood Inst
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Gallazzini, Morgan; Burg, Maurice B (2009) What's new about osmotic regulation of glycerophosphocholine. Physiology (Bethesda) 24:245-9
Gallazzini, Morgan; Ferraris, Joan D; Burg, Maurice B (2008) GDPD5 is a glycerophosphocholine phosphodiesterase that osmotically regulates the osmoprotective organic osmolyte GPC. Proc Natl Acad Sci U S A 105:11026-31
Irarrazabal, Carlos E; Williams, Chester K; Ely, Megan A et al. (2008) Activator protein-1 contributes to high NaCl-induced increase in tonicity-responsive enhancer/osmotic response element-binding protein transactivating activity. J Biol Chem 283:2554-63
Zhou, Xiaoming; Ferraris, Joan D; Dmitrieva, Natalia I et al. (2008) MKP-1 inhibits high NaCl-induced activation of p38 but does not inhibit the activation of TonEBP/OREBP: opposite roles of p38alpha and p38delta. Proc Natl Acad Sci U S A 105:5620-5
Burg, Maurice B; Ferraris, Joan D (2008) Intracellular organic osmolytes: function and regulation. J Biol Chem 283:7309-13
Chen, Ye; Schnetz, Michael P; Irarrazabal, Carlos E et al. (2007) Proteomic identification of proteins associated with the osmoregulatory transcription factor TonEBP/OREBP: functional effects of Hsp90 and PARP-1. Am J Physiol Renal Physiol 292:F981-92
Dmitrieva, Natalia I; Burg, Maurice B (2007) High NaCl promotes cellular senescence. Cell Cycle 6:3108-13
Burg, Maurice B; Ferraris, Joan D; Dmitrieva, Natalia I (2007) Cellular response to hyperosmotic stresses. Physiol Rev 87:1441-74
Ferraris, Joan D; Burg, Maurice B (2007) Tonicity-regulated gene expression. Methods Enzymol 428:279-96
Dmitrieva, Natalia I; Burg, Maurice B (2007) Osmotic stress and DNA damage. Methods Enzymol 428:241-52

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