Further evidence for mitochondrial dysfunction in progressive supranuclear palsy

Exp Neurol. 2001 Mar;168(1):196-8. doi: 10.1006/exnr.2000.7607.

Abstract

Recent data from our laboratory have identified a role for mitochondrial dysfunction in the pathogenesis of progressive supranuclear palsy (PSP). To extend this finding, we measured key parameters of mitochondrial function in platelet-derived cytoplasmic hybrid (cybrid) cell lines expressing mitochondrial genes from patients with PSP. We observed significant decreases in aconitase activity, cellular ATP levels, and oxygen consumption in PSP cybrids as compared to control cybrids, further suggesting a contributory role of impaired mitochondrial energy metabolism in PSP, possibly due to genetic abnormalities of mitochondrial DNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Aged
  • Blood Platelets / pathology
  • Blood Platelets / physiology*
  • Cell Fusion
  • Female
  • Humans
  • Hybrid Cells
  • Male
  • Mitochondria / metabolism*
  • Neuroblastoma
  • Oxygen Consumption
  • Reference Values
  • Supranuclear Palsy, Progressive / blood
  • Supranuclear Palsy, Progressive / metabolism*
  • Tumor Cells, Cultured

Substances

  • Adenosine Triphosphate