Myofilament degradation and dysfunction of human cardiomyocytes in fabry disease

Cristina Chimenti, Nazha Hamdani, Nicky M. Boontje, Francesco DeCobelli, Antonio Esposito, Jean G F Bronzwaer, Ger J M Stienen, Matteo A. Russo, Walter J. Paulus, Andrea Frustaci, Jolanda Van Der Velden

Research output: Contribution to journalArticlepeer-review

Abstract

Early detection of myocardial dysfunction in Fabry disease (FD) cardiomyopathy suggests the contribution of myofilament structural alterations. Six males with untreated FD cardiomyopathy submitted to cardiac studies, including tissue Doppler imaging and left ventricular endomyocardial biopsy. Active and resting tensions before and after treatment with protein kinase A (PKA) were determined in isolated Triton-permeabilized cardiomyocytes. Cardiomyocyte cross-sectional area, glycosphingolipid vacuole area, myofibrillolysis, and extent of fibrosis were also determined. Biopsies of mitral stenosis in patients with normal left ventricles served as controls. Active tension was four times lower in FD cardiomyocytes and correlated with extent of myofibrillolysis. Resting tension was six times higher in FD cardiomyocytes than in controls. PKA treatment decreased resting tension but did not affect active force. Protein analysis revealed troponin I and desmin degradation products. FD cardiomyocytes were significantly larger and filled with glycosphingolipids. Fibrosis was mildly increased compared with controls. Tissue Doppler imaging lengthening and shortening velocities were reduced in FD cardiomyocytes compared with controls, correlating with resting and active tensions, respectively, but not with cardiomyocyte area, percentage of glycosphingolipids, or extent of fibrosis. In conclusion, myofilament degradation and dysfunction contribute to FD cardiomyopathy. Partial reversal of high resting tension after pharmacological PKA treatment of cardiomyocytes suggests potential benefits from enzyme replacement therapy and/or energy-releasing agents.

Original languageEnglish
Pages (from-to)1482-1490
Number of pages9
JournalAmerican Journal of Pathology
Volume172
Issue number6
DOIs
Publication statusPublished - Jun 2008

ASJC Scopus subject areas

  • Pathology and Forensic Medicine

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