Ultrastructural changes in skeletal muscle of infants with mitochondrial respiratory chain complex I defects

Ji Young Mun, Min Kyo Jung, Se Hoon Kim, Soyong Eom, Sung Sik Han, Young Mock Lee

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

Background and Purpose The pathogenesis of mitochondrial disease (MD) involves the disruption of cellular energy metabolism, which results from defects in the mitochondrial respiratory chain complex (MRC). We investigated whether infants with MRC I defects showed ultrastructural changes in skeletal muscle. Methods Twelve infants were enrolled in this study. They were initially evaluated for unexplained neurodegenerative symptoms, myopathies, or other progressive multiorgan involvement, and underwent muscle biopsies when MD was suspected. Muscle tissue samples were subjected to biochemical enzyme assays and observation by transmission electron microscopy. We compared and analyzed the ultrastructure of skeletal muscle tissues obtained from patients with and without MRC I defects. Results Biochemical enzyme assays confirmed the presence of MRC I defects in 7 of the 12 patients. Larger mitochondria, lipid droplets, and fused structures between the outer mitochondrial membrane and lipid droplets were observed in the skeletal muscles of patients with MRC I defects. Conclusions Mitochondrial functional defects in MRC I disrupt certain activities related to adenosine triphosphate synthesis that produce changes in the skeletal muscle. The ultrastructural changes observed in the infants in this study might serve as unique markers for the detection of MD.

Original languageEnglish
Pages (from-to)359-365
Number of pages7
JournalJournal of Clinical Neurology (Korea)
Volume13
Issue number4
DOIs
Publication statusPublished - 2017 Oct

Keywords

  • Infant
  • Mitochondria
  • Muscle pathology
  • Respiratory chain complex
  • Transmission electron microscopy
  • Ultrastructure

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

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