Role of G-proteins in the regulation of organic osmolyte efflux from isolated rat renal inner medullary collecting duct cells
Autor: | Birgit Ruhfus, Rolf K. H. Kinne, Hanna Tinel |
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Rok vydání: | 1996 |
Předmět: |
Male
Taurine Physiology Clinical Biochemistry Wasp Venoms Cell Separation chemistry.chemical_compound Betaine GTP-Binding Proteins Physiology (medical) Extracellular Animals Virulence Factors Bordetella Kidney Tubules Collecting Rats Wistar Kidney Medulla Arachidonic Acid Intracellular Membranes Water-Electrolyte Balance Rats Drug Combinations Hypotonic Shock Hypotonic Solutions Pertussis Toxin chemistry Biochemistry Osmolyte Mastoparan Intercellular Signaling Peptides and Proteins Calcium Sorbitol Peptides Intracellular |
Zdroj: | Pfl�gers Archiv European Journal of Physiology. 433:35-41 |
ISSN: | 1432-2013 0031-6768 |
DOI: | 10.1007/s004240050245 |
Popis: | Hypotonic shock (change of osmolality from 600 mosmol to 300 mosmol by lowering NaCl concentration) increases the release of organic osmolytes from isolated inner medullary collecting duct (IMCD) cells in the following sequence: taurinebetainesorbitolmyo-inositolglycerophosphorylcholine (GPC). The role of G-proteins in regulating the hypotonicity-induced efflux was analysed by exposing cells to various concentrations of a G-protein inhibitor, pertussis toxin (PTX; 20-200 ng/ml), and a Gialpha-protein stimulator, mastoparan (10-50 microM). PTX diminished the hypotonic release of sorbitol and betaine by 43.2+/-9. 5% and 32.2+/-7.8% (n = 5), respectively. Efflux of GPC, myo-inositol and taurine was not significantly altered. Mastoparan (10 microM) increased osmolyte release under isotonic conditions such that release of betaine was increased 3.8-fold and that of sorbitol 2.1-fold, while GPC, myo-inositol and taurine effluxes were only slightly augmented. Under hypotonic conditions, mastoparan stimulated betaine release (1.86+/-0.2-fold, n = 5) but not that of sorbitol. As tested in connection with sorbitol and betaine release, the effect of mastoparan was abolished by PTX, but not the A23187-evoked sorbitol release. Like mastoparan, arachidonic acid increased the release of sorbitol and betaine under isotonic conditions, but under hypotonic conditions it only increased the release of betaine. As to the role of intracellular Ca2+, hypotonic shock evoked an intracellular Ca2+ peak which could be prevented by PTX. Mastoparan increased intracellular Ca2+ under isotonic conditions, whether the extracellular Ca2+ concentration was low or high. The results indicate that G-proteins are involved in regulating sorbitol and betaine efflux from IMCD cells. The G-proteins regulating sorbitol release are probably involved in generating the proper intracellular Ca2+ signal. Betaine efflux, which is independent of intracellular Ca2+, might be regulated by a G-protein-stimulated release of arachidonic acid. Thus, probably several G-proteins are involved in controlling organic osmolyte efflux from IMCD cells. |
Databáze: | OpenAIRE |
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