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Chloride transport activation by plasma osmolarity during rapid adaptation to high salinity of Fundulus heteroclitus
Authors:J A Zadunaisky  S Cardona  L Au  D M Roberts  E Fisher  B Lowenstein  E J Cragoe Jr  K R Spring
Institution:(1) Departments of Physiology and Biophysics and of Ophthalmology, New York University Medical Center, 550 First Avenue, 10016 New York, NY;(2) Mount Desert Island Biological Laboratory, 04672 Salsbury Cove, Maine;(3) Laboratory of Kidney and Electrolyte, Metabolism, National Institutes of Health, 20892 Bethesda, Maryland
Abstract:Transition from low salt water to sea water of the euryhaline fish, Fundulus heteroclitus, involves a rapid signal that induces salt secretion by the gill chloride cells. An increase of 65 mOsm in plasma osmolarity was found during the transition. The isolated, chloridecell-rich opercular epithelium of sea-water-adapted Fundulus exposed to 50 mOsm mannitol on the basolateral side showed a 100% increase in chloride secretion, which was inhibited by bumetanide 10–4 m and 10–4 m DPC (N-Phenylanthranilic acid). No effect of these drugs was found on apical side exposure. A Na+/H+ exchanger, demonstrated by NH4Cl exposure, was inhibited by amiloride and its analogues and stimulated by IBMX, phorbol esters, and epithelial growth factor (EGF). Inhibition of the Na+/H+ exchanger blocks the chloride secretion increase due to basolateral hypertonicity. A Cl/HCO 3 exchanger was also found in the chloride cells, inhibited by 10–4 m DIDS but not involved in the hyperosmotic response. Ca2+ concentration in the medium was critical for the stimulation of Cl secretion to occur. Chloride cell volume shrinks in response to hypertonicity of the basolateral side in sea-water-adapted operculi; no effect was found on the apical side. Freshwater-adapted fish chloride cells show increased water permeability of the apical side. It is concluded that the rapid signal for adaptation to higher salinities is an increased tonicity of the plasma that induces chloride cell shrinkage, increased chloride secretion with activation of the Na+K+2Cl cotransporter, the Na+/H+ exchanger and opening of Cl channels.The work was supported by the National Institutes of Health, Research Grant EYO1340 to J.A.Z. Part of this research was performed while Dr. Zadunaisky was a Scholar In Residence at the Fogarty International Center of The National Institutes of Health in Bethesda, Maryland. Ms. Dawn Roberts was a fellow of the Grass Foundation and Pew Foundation during this work. Grants from the National Science Foundation and the National Institutes of Health to the Mount Desert Island Biological Laboratory also provided assistance for this research.
Keywords:Gill chloride cell  Cl   secretion  Fundulus heteroclitus  Cell volume regulation  Na+/H+ exchanger  Cl  /HCO 3    exchanger
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