Phorbol ester activation of an NHE-like electroneutral Na+/H+ antiporter in isolated E-cells of lobster (Homarus americanus) hepatopancreas

Autor: G. A. Ahearn, Jeffrey M. Duerr
Rok vydání: 1998
Předmět:
Zdroj: The Journal of Experimental Zoology. 281:97-108
ISSN: 1097-010X
0022-104X
Popis: The basolateral membrane of Atlantic lobster (Homarus americanus) epithelium possesses an electroneutral Na+/H+ antiporter that functionally resembles members of the vertebrate NHE family. Regulatory mechanisms of this antiporter in purified hepatopancreatic E-cell suspensions, produced with a centrifugal elutriation technique, were investigated. Suspensions routinely consisted of greater than 95% E-cells displaying greater than 90% viability. Intracellular pH (pHi) was monitored by loading cells with the fluorescent dye 2′,7′-bis(carboxyethyl)-5,6-carboxyfluorescein (BCECF), and placing suspensions in a spectrofluorometer. Recovery from induced acid-loading was mediated by a Na+-dependent, dimethylamiloride-sensitive proton efflux. Antiport activation was a sigmoidal function of pHi at values below 7.0. Addition of 20 nM phorbol 12-myristate 13-acetate (PMA) to cells suspended in a lobster physiological saline (pHo = 7.4) increased pHi from 7.2 to 7.5 over a 10-min interval. Phorbol ester-induced activation of the Na+/H+ antiporter was due to an increased affinity for internal H+ (apparent pK was shifted toward more alkaline values) at the level of an internal H+-binding allosteric modifier site. No effect was observed when cells were exposed to 2 μM 8-Br-cAMP. Phorbol ester activation of the lobster NHE-like Na+/H+ antiporter was inhibited by 10 nM bisindoylmaleimide I, a potent protein kinase C inhibitor. These results taken together suggest a remarkable conservation of Na+/H+ antiport across phyla. J. Exp. Zool. 281:97–108, 1998. © 1998 Wiley-Liss, Inc.
Databáze: OpenAIRE
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