Key result
Induction of Cx45 expression in a rat liver epithelial cell line significantly reduced gap junction sizes by 15% to 20% (p < 0.001), whereas coexpression of Cx40 with Cx43 had no effect.
Why the study?
Does coexpression of Cx45 with Cx43 decrease gap junction size in cells endogenously expressing Cx43?
Does coexpression of Cx45 with Cx43 decrease gap junction size in cells endogenously expressing Cx43?
Increased Cx45 expression, as observed in the failing ventricle, contributes to decreased gap junction size when coexpressed with Cx43.
Answers are grounded in this paper and cite their sources.
Cx45 coexpression may reduce gap junction size in Cx43 cells; leaves open contribution to remodeling in failing human ventricle.
In the human heart, ventricular myocytes express connexin 43 (Cx43) and traces of Cx45. In congestive heart failure, Cx43 levels decrease, Cx45 levels increase and gap junction size decreases. To determine whether alterations of connexin coexpression ratio influence gap junction size, we engineered a rat liver epithelial cell line that endogenously expresses Cx43 to coexpress inducible levels of Cx45 under stimulation of the insect hormone, ponasterone A. In cells induced to express Cx45, gap junction sizes are significantly reduced (by 15% to 20%; p < 0.001), an effect that occurs despite increased levels of junctional connexons made from both connexins. In contrast, coexpression of Cx40 with Cx43 does not lead to any change in gap junction size. These results are consistent with the idea that increased Cx45 expression in the failing ventricle contributes to decreased gap junction size.
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Grikscheit et al. (2008) studied Congestive heart failure. Induction of Cx45 expression vs. Coexpression of Cx40 with Cx43 was evaluated on Gap junction size (p=<0.001). Induction of Cx45 expression in a rat liver epithelial cell line significantly reduced gap junction sizes by 15% to 20% (p < 0.001), whereas coexpression of Cx40 with Cx43 had no effect.
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