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The heterotrimeric G protein Go 2 regulates catecholamine uptake by secretory vesicles
Author(s) -
AhnertHilger Gudrun,
Nürnberg Bernd,
Exner Torsten,
Schäfer Theo,
Jahn Reinhard
Publication year - 1998
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1093/emboj/17.2.406
Subject(s) - heterotrimeric g protein , biology , vesicle , microbiology and biotechnology , catecholamine , g protein , biochemistry , neuroscience , signal transduction , membrane
Secretory vesicles store neurotransmitters that are released by exocytosis. Their membrane contains transporters responsible for transmitter loading that are driven by an electrochemical proton gradient across the vesicle membrane. We have now examined whether uptake of noradrenaline is regulated by heterotrimeric G proteins. In streptolysin O‐permeabilized PC 12 cells, GTP‐analogues and AlF 4 − inhibited noradrenaline uptake, an effect that was sensitive to treatment with pertussis toxin. Inhibition of uptake was prevented by Gαo‐specific antibodies and mimicked by purified activated Gαo 2 . No effect was seen when Gαo 2 in its inactive GDP‐bound form or purified activated Gαo 1 , Gαi 1 and Gαi 2 were tested. Down‐regulation of uptake remained unchanged when exocytosis was inhibited by the light chain of tetanus toxin. Vesicular acidification was not affected whereas binding of [ 3 H]reserpine was reduced by GTPγS and Gαo 2 . These data suggest that the monoamine transporter rather than the vacuolar ATPase is affected. We conclude that catecholamine uptake is controlled by Gαo 2 , suggesting a novel function for heterotrimeric G proteins in the control of neurotransmitter storage.

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