Negative regulation of cellular ca2+ mobilization by ryanodine receptor type 3 in mouse mesenteric artery smooth muscle

Abstract

Physiological functions of type 3 ryanodine receptors (RyR3) in smooth muscle (SM) tissues are not well understood, in spite of their wide expression. However, the short isoform of RyR3 is known to be a dominant-negative variant (DN-RyR3), which may negatively regulate functions of both RyR2 and full-length (FL) RyR3 by forming hetero-tetramers. Here, functional roles of RyR3 in the regulation of Ca2+ signaling in mesenteric artery SM cells (MASMCs) were examined using RyR3 homozygous knockout mice (RyR3−/−). Quantitative PCR analyses suggested that the predominant RyR3 subtype in MASMs from wild-type mice (RyR3−/−) was DN-RyR3. In single MASMCs freshly isolated from RyR3−/−, the EC50 of caffeine to induce Ca2+ release was lower than that in RyR3−/− myocytes. The amplitude and frequency of Ca2+ sparks and spontaneous transient outward currents in MASMCs from RyR3−/− were all larger than those from RyR3−/−. Importantly, mRNA and functional expressions of voltage-dependent Ca2+ channel and large-conductance Ca2+- activated K+ (BK) channel in MASMCs from RyR3−/− were identical to those from RyR3−/−. However, in the presence of BK channel inhibitor, paxilline, the pressure rises induced by BayK8644 in MA vascular beds of RyR3−/− were significantly larger than in those of RyR3−/−. This indicates that the negative feedback effects of BK channel activity on intracellular Ca2+ signaling was enhanced in RyR3−/−. Thus, RyR3, and, in fact, mainly DN-RyR3, via a complex with RyR2 suppresses Ca2+ release and indirectly regulated membrane potential by reducing BK channel activity in MASMCs and presumably can affect the regulation of intrinsic vascular tone.