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Native ?6?4* nicotinic receptors control exocytosis in human chromaffin cells of the adrenal gland.


ABSTRACT: In the present study, we have electrophysiologically characterized native nicotinic acetylcholine receptors (nAChRs) in human chromaffin cells of the adrenal gland as well as their contribution to the exocytotic process. ?-Conotoxin AuIB blocked by 14 ± 1% the acetylcholine (ACh)-induced nicotinic current. ?-Conotoxin MII (?-Ctx MII) exhibited an almost full blockade of the nicotinic current at nanomolar concentrations (IC(50)=21.6 nM). The ?6*-preferring ?-Ctx MII mutant analogs, ?-Ctx MII[H9A,L15A] and ?-Ctx MII[S4A,E11A,L15A], blocked nAChR currents with an IC(50) of 217.8 and 33 nM, respectively. These data reveal that nAChRs in these cells include the ?6* subtype. The washout of the blockade exerted by ?-conotoxin BuIA (?-Ctx BuIA; 1 ?M) on ACh-evoked currents was slight and slow, arguing in favor of the presence of a ?4 subunit in the nAChR composition. Exocytosis was almost fully blocked by 1 ?M ?-Ctx MII, its mutant analogs, or ?-Ctx BuIA. Finally, the fluorescent analog Alexa Fluor 546-BuIA showed distinct staining in these cells. Our results reveal that ?6?4* nAChRs are expressed and contribute to exocytosis in human chromaffin cells of the adrenal gland, the main source of adrenaline under stressful situations.

SUBMITTER: Perez-Alvarez A 

PROVIDER: S-EPMC3250250 | biostudies-literature | 2012 Jan

REPOSITORIES: biostudies-literature

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Native α6β4* nicotinic receptors control exocytosis in human chromaffin cells of the adrenal gland.

Pérez-Alvarez Alberto A   Hernández-Vivanco Alicia A   McIntosh J Michael JM   Albillos Almudena A  

FASEB journal : official publication of the Federation of American Societies for Experimental Biology 20110914 1


In the present study, we have electrophysiologically characterized native nicotinic acetylcholine receptors (nAChRs) in human chromaffin cells of the adrenal gland as well as their contribution to the exocytotic process. α-Conotoxin AuIB blocked by 14 ± 1% the acetylcholine (ACh)-induced nicotinic current. α-Conotoxin MII (α-Ctx MII) exhibited an almost full blockade of the nicotinic current at nanomolar concentrations (IC(50)=21.6 nM). The α6*-preferring α-Ctx MII mutant analogs, α-Ctx MII[H9A,  ...[more]

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