Key result
Glucosylceramide synthase deficiency causes severe heart failure via suppressed beta1-adrenergic receptor trafficking.
Why the study?
Cardiac dysfunction occurs in rare monogenic diseases affecting glycosphingolipid synthesis and turnover, but how cardiac glycosphingolipids regulate cellular processes and function in the heart was unknown.
Does cardiomyocyte-specific deficiency in glucosylceramide synthase (Ugcg) impair β1-adrenergic receptor trafficking and contractile capacity in mouse and cell models?
Does cardiomyocyte-specific deficiency in glucosylceramide synthase (Ugcg) impair β1-adrenergic receptor trafficking and contractile capacity in mouse and cell models?
Answers are grounded in this paper and cite their sources.
Cardiac glycosphingolipids synthesized by glucosylceramide synthase are essential for maintaining β1-adrenergic receptor trafficking, β-adrenergic signalling, and normal contractile function in the heart.
AIMS: Cardiac injury and remodelling are associated with the rearrangement of cardiac lipids. Glycosphingolipids are membrane lipids that are important for cellular structure and function, and cardiac dysfunction is a characteristic of rare monogenic diseases with defects in glycosphingolipid synthesis and turnover. However, it is not known how cardiac glycosphingolipids regulate cellular processes in the heart. The aim of this study is to determine the role of cardiac glycosphingolipids in heart function. METHODS AND RESULTS: Using human myocardial biopsies, we showed that the glycosphingolipids glucosylceramide and lactosylceramide are present at very low levels in non-ischaemic human heart with normal function and are elevated during remodelling. Similar results were observed in mouse models of cardiac remodelling. We also generated mice with cardiomyocyte-specific deficiency in Ugcg, the gene encoding glucosylceramide synthase (hUgcg-/- mice). In 9- to 10-week-old hUgcg-/- mice, contractile capacity in response to dobutamine stress was reduced. Older hUgcg-/- mice developed severe heart failure and left ventricular dilatation even under baseline conditions and died prematurely. Using RNA-seq and cell culture models, we showed defective endolysosomal retrograde trafficking and autophagy in Ugcg-deficient cardiomyocytes. We also showed that responsiveness to β-adrenergic stimulation was reduced in cardiomyocytes from hUgcg-/- mice and that Ugcg knockdown suppressed the internalization and trafficking of β1-adrenergic receptors. CONCLUSIONS: Our findings suggest that cardiac glycosphingolipids are required to maintain β-adrenergic signalling and contractile capacity in cardiomyocytes and to preserve normal heart function.
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Andersson et al. (2021) studied Cardiac remodelling and heart failure. Cardiomyocyte-specific Ugcg (glucosylceramide synthase) deficiency vs. Normal glycosphingolipid synthesis (wild-type/baseline) was evaluated on Cardiac function and beta1-adrenergic receptor trafficking. Cardiomyocyte-specific deficiency in glucosylceramide synthase caused severe heart failure, reduced contractile capacity, and suppressed beta1-adrenergic receptor trafficking.
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