Mitochondrial abnormalities related to the dysfunction of circulating endothelial colony-forming cells in moyamoya disease

J Neurosurg. 2018 Nov 1;129(5):1151-1159. doi: 10.3171/2017.5.JNS17147. Epub 2017 Dec 8.

Abstract

The authors performed morphological and functional studies of the mitochondria in particular blood cells, i.e., endothelial colony-forming cells (ECFCs), from patients with moyamoya disease. The results indicated that the mitochondria of these ECFCs exhibit morphological and functional abnormalities, which may present new insights into the pathogenesis of moyamoya disease.

Keywords: ATP = adenosine triphosphate; CCCP = carbonyl cyanide m-chlorophenyl hydrazine; DCFH-DA = 2′,7′-dichlorodihydrofluorescein diacetate; ECFC = endothelial colony-forming cell; EPC = endothelial progenitor cell; Fluo-4 = fluo-4 acetoxymethyl ester; MMD = moyamoya disease; MMP = mitochondrial membrane potential; MTT = 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide; NAC = N-acetyl-l-cysteine; OCR = oxygen consumption rate; PBS = phosphate-buffered saline; ROS = reactive oxygen species; TMRM = tetramethylrhodamine methyl ester; [Ca2+]i = intracellular Ca2+ concentration; cell culture; cerebrovascular disease; mitochondria; moyamoya; vascular disorders; vasculogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • Endothelial Progenitor Cells / metabolism*
  • Endothelial Progenitor Cells / pathology
  • Female
  • Humans
  • Infant
  • Male
  • Mitochondria / metabolism*
  • Mitochondria / pathology
  • Moyamoya Disease / metabolism*
  • Moyamoya Disease / pathology
  • Oxygen Consumption / physiology
  • Reactive Oxygen Species / metabolism
  • Young Adult

Substances

  • Reactive Oxygen Species