Protein kinase C enhances plasma membrane expression of cardiac L-type calcium channel, Ca(V)1.2

Item Type:	Article
Title:	Protein kinase C enhances plasma membrane expression of cardiac L-type calcium channel, Ca(V)1.2
Creators Name:	Raifman, T.K. and Kumar, P. and Haase, H. and Klussmann, E. and Dascal, N. and Weiss, S.
Abstract:	L-type-voltage-dependent Ca(2+) channels (L-VDCCs; CaV1.2, α(1C)), crucial in cardiovascular physiology and pathology, are modulated via activation of G-protein-coupled receptors and subsequently protein kinase C (PKC). Despite extensive study, key aspects of the mechanisms leading to PKC-induced Ca(2+) current increase are unresolved. A notable residue, Ser1928, located in the distal C-terminus (dCT) of α(1C) was shown to be phosphorylated by PKC. Ca(V)1.2 undergoes posttranslational modifications yielding full-length and proteolytically cleaved CT-truncated forms. We have previously shown that, in Xenopus oocytes, activation of PKC enhances α(1C) macroscopic currents. This increase depended on the isoform of α1C expressed. Only isoforms containing the cardiac, long N-terminus (L-NT), were upregulated by PKC. Ser1928 was also crucial for the full effect of PKC. Here we report that, in Xenopus oocytes, following PKC activation the amount of α(1C) protein expressed in the plasma membrane (PM) increases within minutes. The increase in PM content is greater with full-length α(1C) than in dCT-truncated α(1C), and requires Ser1928. The same was observed in HL-1 cells, a mouse atrium cell line natively expressing cardiac α(1C), which undergoes the proteolytic cleavage of the dCT, thus providing a native setting for exploring the effects of PKC in cardiomyocytes. Interestingly, activation of PKC preferentially increased the PM levels of full-length, L-NT α(1C). Our findings suggest that part of PKC regulation of Ca(V)1.2 in the heart involves changes in channel's cellular fate. The mechanism of this PKC regulation appears to involve the C-terminus of α(1C), possibly corroborating the previously proposed role of NT-CT interactions within α(1C).
Keywords:	Calcium Channel, Cardiovascular, HL-1 Cells, Plasma Membrane, Protein Kinase C, Protein Localization, Ser1928, Animals, Xenopus laevis, Animals, Mice
Source:	Channels
ISSN:	1933-6950
Publisher:	Taylor & Francis
Volume:	11
Number:	6
Page Range:	604-615
Date:	2 November 2017
Official Publication:	https://doi.org/10.1080/19336950.2017.1369636
PubMed:	View item in PubMed

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