Conventional protein kinase C isoforms regulate human dopamine transporter activity in Xenopus oocytes.

Abstract:

:The hypothesis that specific protein kinase C (PKC) isoforms regulate dopamine transporter (DAT) function was tested in Xenopus laevis oocytes expressing human (h)DAT. Activation of conventional PKCs (cPKCs) and novel PKCs (nPKCs) using 10 nM phorbol 12-myristate 13-acetate (PMA) significantly inhibited DAT-associated transport currents. This effect was reversed by isoform-non-selective PKC inhibitors, selective inhibitors of cPKCs and deltaPKC, and by Ca2+ chelation. By contrast, the epsilonPKC translocation inhibitor peptide had no effect on PMA-induced inhibition of hDAT transport-associated currents. Thus, the primary mechanism by which PMA regulates hDAT expressed in oocytes appears to be by activating cPKC(s).

journal_name

FEBS Lett

journal_title

FEBS letters

authors

Doolen S,Zahniser NR

doi

10.1016/s0014-5793(02)02554-1

keywords:

subject

Has Abstract

pub_date

2002-04-10 00:00:00

pages

187-90

issue

1-3

eissn

0014-5793

issn

1873-3468

pii

S0014579302025541

journal_volume

516

pub_type

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