Key result
Cardiac-specific Lrp6 knockout in mice disrupts Cx43 gap junction formation and predisposes the hearts to lethal arrhythmias, with a 75% incidence of ventricular tachycardia or fibrillation under stress compared to 0% in controls.
Why the study?
Does LRP6 deficiency impair Cx43 gap junction formation and predispose to arrhythmias in preclinical models?
Does LRP6 deficiency impair Cx43 gap junction formation and predispose to arrhythmias in preclinical models?
Answers are grounded in this paper and cite their sources.
LRP6 acts as a crucial scaffold protein for Cx43 gap junction assembly in cardiomyocytes, and its deficiency leads to lethal arrhythmias independent of Wnt signaling.
Low-density lipoprotein receptor-related protein 6 (LRP6) is a Wnt co-receptor in the canonical Wnt/β-catenin signalling. Here, we report the scaffold function of LRP6 in gap junction formation of cardiomyocytes. Cardiac LRP6 is spatially restricted to intercalated discs and binds to gap junction protein connexin 43 (Cx43). A deficiency in LRP6 disrupts Cx43 gap junction formation and thereby impairs the cell-to-cell coupling, which is independent of Wnt/β-catenin signalling. The defect in Cx43 gap junction resulting from LRP6 reduction is attributable to the defective traffic of de novo Cx43 proteins from the endoplasmic reticulum to the Golgi apparatus, leading to the lysosomal degradation of Cx43 proteins. Accordingly, the hearts of conditional cardiac-specific Lrp6-knockout mice consistently exhibit overt reduction of Cx43 gap junction plaques without any abnormality in Wnt signalling and are predisposed to lethal arrhythmias. These findings uncover a distinct role of LRP6 as a platform for intracellular protein trafficking.
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Li et al. (2016) studied Arrhythmia. Lrp6 knockout vs. Cre transgene control was evaluated on Incidence of ventricular tachycardia or fibrillation under stress. Cardiac-specific Lrp6 knockout in mice disrupts Cx43 gap junction formation and predisposes the hearts to lethal arrhythmias, with a 75% incidence of ventricular tachycardia or fibrillation under stress compared to 0% in controls.
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