3
Views
1
CrossRef citations to date
0
Altmetric
Original

Connexin Isoform Expression in Smooth Muscle Cells and Endothelial Cells of Hamster Cheek Pouch Arterioles and Retractor Feed Arteries

, &
Pages 503-514 | Received 19 Sep 2006, Accepted 12 Feb 2008, Published online: 10 Jul 2009
 

Abstract

Objective: Gap junction channels formed by connexin (Cx) protein subunits enable cell-to-cell conduction of vasoactive signals. Given the lack of quantitative measurements of Cx expression in microvascular endothelial cells (EC) and smooth muscle cells (SMC), the objective was to determine whether Cx expression differed between EC and SMC of resistance microvessels for which conduction is well-characterized.

Methods: Cheek pouch arterioles (CPA) and retractor feed arteries (RFA) were hand-dissected and dissociated to obtain SMC or endothelial tubes. In complementary experiments, small intestine was dissociated to obtain SMC. Following reverse transcription, quantitative Real-Time Polymerase Chain Reaction (qRT-PCR) was performed by using specific primers and fluorescent probes for Cx37, Cx40, and Cx43. Smooth muscle α-actin (SMAA) and platelet endothelial cell adhesion molecule-1 (PECAM-1) served as respective reference genes.

Results: Transcript copy numbers were similar for each Cx isoform in EC from CPA and RFA (∼0.5 Cx/PECAM-1). For SMC, Cx43 transcript in CPA and RFA (<0.1 Cx/SMAA) was less (p < 0.05) than that in small intestine (∼0.4 Cx/SMAA). Transcripts for Cx37 and Cx40 were also detected in SMC. Punctate immunolabeling for each Cx isoform was pronounced at EC borders and that for Cx43 was pronounced in SMC of small intestine. In contrast, Cx immunolabeling was not detected in SMC of CPA or RFA.

Conclusions: Connexin expression occurs primarily within the endothelium of arterioles and feed arteries, supporting a highly effective pathway for conducting vasoactive signals along resistance networks. The apparent paucity of Cx expression within SMC underscores discrete homocellular coupling and focal localization of myoendothelial gap junctions.

View correction statement:
Erratum

This study was supported by grants RO1-HL56786, RO1-HL41026 (S.S. Segal), and RO1-HL32469 (W.F. Jackson) from the National Institutes of Health, United States Public Health Service. Preliminary experiments for this study were performed at The John B. Pierce Laboratory (New Haven, Connecticut, USA).

Log in via your institution

Log in to Taylor & Francis Online

There are no offers available at the current time.

Related Research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.