4.6 Article

Severe T-System Remodeling in Pediatric Viral Myocarditis

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FRONTIERS MEDIA SA
DOI: 10.3389/fcvm.2020.624776

关键词

myocarditis; transverse tubular system; excitation-contracting coupling; heart failiure; remodeling; confocal micoscopy; ryanodine receptor (RyR)

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  1. Interdisciplinary Center for Clinical Research (IZKF) at the University Hospital of the Friedrich-Alexander University of Erlangen-Nurnberg (FAU)

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The study found that in pediatric viral myocarditis, remodeling of the cardiomyocyte transverse tubular system (t-system) may lead to impairment of excitation-contraction coupling. Compared to atrioventricular septum defect, myocarditis samples showed increased t-tubule distance and dilation of t-tubules, resembling the structural changes of chronically failing adult hearts. The measurement of intact EC coupling junctions in myocarditis samples showed a distinct increase.
Chronic heart failure (HF) in adults causes remodeling of the cardiomyocyte transverse tubular system (t-system), which contributes to disease progression by impairing excitation-contraction (EC) coupling. However, it is unknown if t-system remodeling occurs in pediatric heart failure. This study investigated the t-system in pediatric viral myocarditis. The t-system and integrity of EC coupling junctions (co-localization of L-type Ca2+ channels with ryanodine receptors and junctophilin-2) were analyzed by 3D confocal microscopy in left-ventricular (LV) samples from 5 children with myocarditis (age 14 +/- 3 months), undergoing ventricular assist device (VAD) implantation, and 5 children with atrioventricular septum defect (AVSD, age 17 +/- 3 months), undergoing corrective surgery. LV ejection fraction (EF) was 58.4 +/- 2.3% in AVSD and 12.2 +/- 2.4% in acute myocarditis. Cardiomyocytes from myocarditis samples showed increased t-tubule distance (1.27 +/- 0.05 mu m, n = 34 cells) and dilation of t-tubules (volume-length ratio: 0.64 +/- 0.02 mu m(2)) when compared with AVSD (0.90 +/- 0.02 mu m, p < 0.001; 0.52 +/- 0.02 mu m(2), n = 61, p < 0.01). Intriguingly, 4 out of 5 myocarditis samples exhibited sheet-like t-tubules (t-sheets), a characteristic feature of adult chronic heart failure. The fraction of extracellular matrix was slightly higher in myocarditis (26.6 +/- 1.4%) than in AVSD samples (24.4 +/- 0.8%, p < 0.05). In one case of myocarditis, a second biopsy was taken and analyzed at VAD explantation after extensive cardiac recovery (EF from 7 to 56%) and clinical remission. When compared with pre-VAD, t-tubule distance and density were unchanged, as well as volume-length ratio (0.67 +/- 0.04 mu m(2) vs. 0.72 +/- 0.05 mu m(2), p = 0.5), reflecting extant t-sheets. However, junctophilin-2 cluster density was considerably higher (0.12 +/- 0.02 mu m(-3) vs. 0.05 +/- 0.01 mu m(-3), n = 9/10, p < 0.001), approaching values of AVSD (0.13 +/- 0.05 mu m(-3), n = 56), and the measure of intact EC coupling junctions showed a distinct increase (20.2 +/- 5.0% vs. 6.8 +/- 2.2%, p < 0.001). Severe t-system loss and remodeling to t-sheets can occur in acute HF in young children, resembling the structural changes of chronically failing adult hearts. T-system remodeling might contribute to cardiac dysfunction in viral myocarditis. Although t-system recovery remains elusive, recovery of EC coupling junctions may be possible and deserves further investigation.

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