Reduced Cx43 Expression Triggers Increased Fibrosis Due to Enhanced Fibroblast Activity

• DOI: 10.1161/circep.111.966580
• Publication Date: 2012-02-25T06:11:34Z
• Authors: John A. Jansen; Toon A.B. van Veen; Sanne de Jong; Roel van der Nagel; Leonie van Stuijv...; Helen Driessen; Ronald Labzowski; Carolin M. Oefner; Astrid A. Bosch; Tri Q. Nguyen; Roel Goldschmeding; Marc A. Vos; Jacques M.T. de B...; Harold V.M. van R...
• Keywords: Male; Aging; Myocardium; Arrhythmias, Cardiac; Constriction, Pathologic; Fibroblasts; Fibrosis; Mice; 03 medical and health sciences; IGMD 3: Genomic disorders and inherited multi-system disorders; 0302 clinical medicine; Heart Conduction System; Stress, Physiological; Connexin 43; Models, Animal; Animals; Female; Collagen; Aorta; Cell Proliferation

Background— Arrhythmogenic ventricular remodeling is hallmarked by both reduced gap junction expression and increased collagen deposition. We hypothesized that reduced connexin43 (Cx43) expression is responsible for enhanced fibrosis in the remodeled heart, resulting in an arrhythmogenic substrate. Therefore, we investigated the effect of normal or reduced Cx43 expression on the formation of fibrosis in a physiological (aging) and pathophysiological (transverse aortic constriction [TAC]) mouse model.

Methods and Results—

The Cx43 fl/fl and Cx43 CreER(T)/fl mice were aged 18 to 21 months or, at the age of 3 months, either TAC or sham operated and euthanized after 16 weeks. Epicardial activation mapping of the right and left ventricles was performed on Langendorff perfused hearts. Sustained ventricular arrhythmias were induced in 0 of 11 aged Cx43 fl/fl and 10 of 15 Cx43 Cre-ER(T)/fl mice ( P <0.01). Cx43 expression was reduced by half in aged Cx43 CreER(T)/fl compared with aged Cx43 fl/fl mice, whereas collagen deposition was significantly increased from 1.1±0.2% to 7.4±1.3%. Aged Cx43 CreER(T)/fl mice with arrhythmias had significantly higher levels of fibrosis and conduction heterogeneity than aged Cx43 CreER(T)/fl mice without arrhythmias. The TAC operation significantly increased fibrosis in control compared with sham (4.0±1.2% versus 0.4±0.06%), but this increase was significantly higher in Cx43 CreER(T)/fl mice (10.8±1.4%). Discoidin domain receptor 2 expression was unchanged, but procollagen peptide I and III expression and collagen type 1α2 mRNA levels were higher in TAC–operated Cx43HZ mice.

Conclusions— Reduced cellular coupling results in more excessive collagen deposition during aging or pressure overload in mice due to enhanced fibroblast activity, leading to increased conduction in homogeneity and proarrhythmia.