Abstract

Connexins (Cx) form gap junctions and allow the coordination of cellular behaviour. In vessels, expression of Cx40, Cx37, and Cx43 is well established and specifically Cx40 serves important functions in endothelial cells. In contrast, expression and physiological functions of Cx45 is unclear although its expression has been suggested in vascular smooth muscle (VSM). Therefore, we studied expression and function of Cx45 in vessels using different mice models allowing to identify and delete Cx45. Smooth muscle cell (SMC)-specific deletion was achieved by the Cre/loxP system using Cre-recombinase driven by a Nestin promoter. Deletion of Cx45 leads concomitantly to the expression of enhanced green fluorescence protein (EGFP) in these mice. Conduction of vasomotor responses was studied in cremasteric arterioles using intravital microscopy and arterial pressure was measured telemetrically. Cx45 is transcriptionally expressed in VSM as detected by EGFP expression in SMC-specific Cx45-deficient mice (Cx45fl/fl:Nestin-Cre) but not in endothelial cells (Cx45fl/fl:TIE2-Cre). Moreover, EGFP was located at VSM cell borders in arterioles of transgenic mice carrying an EGFP-tagged Cx45. Expectedly, arteriolar conduction of dilations evoked by the endothelium-dependent agonist acetylcholine were not different between Cx45fl/fl:Nestin-Cre mice and controls carrying homozygously a floxed Cx45 gene (Cx45fl/fl). Surprisingly, the amplitude of locally initiated endothelium-independent constrictions (K+) and dilations (adenosine) declined similarly with distance in both genotypes indicating an intact VSM conduction pathway also in mice being deficient for Cx45 in VSM. Arterial pressure was not different between freely moving Cx45fl/fl and Cx45fl/fl:Nestin-Cre mice during day or night. We conclude that Cx45 is physiologically expressed in VSM, but not in EC in murine arterioles. However, Cx45 is dispensable for the conduction of vasomotor responses along these arterioles. Possibly, other Cx functionally replace the lack of Cx45 in VSM. The reported role of Cx45 in renin secretion does not seem to alter arterial pressure in freely moving mice.

Highlights

  • Gap junctions enable fast signalling between adjacent cells und connect individual cells into a functional unit or syncitium

  • Animals being homozygous for Cx45fl and expressing Nestin-Cre (Cx45fl/fl:Nestin-Cre) were viable and arteriolar vascular smooth muscle cells in the microcirculation were distinctly labelled with enhanced green fluorescence protein (EGFP) (Fig. 1)

  • The present study demonstrates that Cx45 is expressed in smooth muscle cells of arterioles and larger conducting vessels (A. gracilis, femoral, and mesenteric arteries) whereas Cx45 seems to be not expressed in the largest arteries

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Summary

Introduction

Gap junctions enable fast signalling between adjacent cells und connect individual cells into a functional unit or syncitium. Such signalling is pivotal in vessels in the microcirculation since thereby vasomotor signals may communicate along the vascular wall, which lead to the coordination of vascular cell behaviour and synchronous vasoconstriction or vasodilation. The high conduction velocity conformed by the measurement of remote membrane potential changes led to the conclusion that electrotonic transmission of a locally initiated membrane potential change acts as the major coordinating signal along the arterioles [4,5]

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