Abstract
Gap junctions (GJ) are membrane specializations responsible for intercellular communication and for ensuring electrical and/or metabolic coupling between cells. They are composed of connexins, a family of related proteins. Connexin-43 (Cx43) is a major connexin of the rat heart, expressed by myocytes as well as non-muscle cells. In this communication we have examined expression of Cx43 by cardiac fibroblasts and regulation of its expression by an endogenous mitogen, basic fibroblast growth factor (bFGF). Recombinant human bFGF, administered to cultured cells which had been maintained in 0.5% serum for 48 h, induced dose-dependent and statistically significant increases in Cx43 mRNA as well as protein accumulation, at 6 h after addition. Intercellular communication was also increased at 6 h but not 30 min after bFGF treatment, as assessed using a scrape-loading protocol. It is concluded that the bFGF-induced stimulation of Cx43 expression caused increased coupling between cardiac fibroblasts. This would be of importance in injured myocardium, the increased bFGF content of which might stimulate electrical coupling involving fibroblasts of the scar tissue.
MeSH Terms
Animals
Blotting, Northern
Cell Communication
Cells, Cultured
Connexin 43/biosynthesis,genetics
Dose-Response Relationship, Drug
Fibroblast Growth Factor 2/pharmacology
Fibroblasts/metabolism
Gap Junctions/physiology
Gene Expression Regulation
Microscopy, Fluorescence
Myocardium/cytology,metabolism
RNA, Messenger/analysis
Rats
Stimulation, Chemical
Time Factors
Chemicals
Connexin 43
RNA, Messenger
Fibroblast Growth Factor 2
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Doble B W
Division of Cardiovascular Sciences, St. Boniface General Hospital Research Centre, Faculty of Medicine, University of Manitoba, Winnipeg, Canada.
Kardami E
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