Rab27a GTPase modulates L-type Ca2+ channel function via interaction with the II-III linker of Ca(V)1.3 subunit

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Abstract

In a variety of cells, secretory processes require the activation of both Rab27a and L-type channels of the Ca(V)1.3 subtype. In the retinal pigment epithelium (RPE), Rab27a and Ca(V)1.3 channels regulate growth-factor secretion towards its basolateral side. Analysis of murine retina sections revealed a co-localization of both Rab27a and Ca(V)1.3 at the basolateral membrane of the RPE. Heterologously expressed Ca(V)1.3/beta 3/alpha(2)delta(1) channels showed negatively shifted voltage-dependence and decreased current density of about 70\% when co-expressed with Rab27a. However, co-localization analysis using alpha(5)beta(1) integrin as a membrane marker revealed that Rab27a co-expression reduced the surface expression of Ca(V)1.3 only about 10\%. Physical binding of heterologously expressed Rab27a with Ca(V)1.3 channels was shown by co-localization in immunocytochemistry as well as co-immunoprecipitation which was abolished after deletion of a MyRIP-homologous amino acid sequence at the II-III linker of the Ca(V)1.3 subunit. Rab27a over-expression in ARPE-19 cells positively shifted the voltage dependence, decreased current density of endogenous Ca(V)1.3 channels and reduced VEGF-A secretion. We show the first evidence of a direct functional modulation of an ion channel by Rab27a suggesting a new mechanism of Rab and ion channel interaction in the control of VEGF-A secretion in the RPE. (C) 2015 Elsevier Inc. All rights reserved.
Original languageEnglish
Pages (from-to)2231-2240
Number of pages10
JournalCellular Signalling
Volume27
Issue number11
DOIs
Publication statusPublished - 2015

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