Human Platelet Derived Mitochondrial OPA-1 Isoforms and Interaction With TDP-43 in Neurodegenerative Diseases

Mo Med. 2024 Jan-Feb;121(1):87-92.

Abstract

Optic atrophy 1(OPA1) is a GTPase protein that controls mitochondrial fusion, cristae integrity, and mtDNA maintenance. In neurodegenerative diseases such as Alzheimer's disease (AD), amyotrophic lateral sclerosis (ALS), Parkinson's disease (PD), the mitochondrial network morphology is compromised. Studies on TAR-DNA binding protein 43 (TDP-43) has been the focus in our lab. OPA1 and TDP-43 interaction may shed a light on how aberrant TDP-43 interacts with OPA1, which will lead to mitochondrial dysfunction. The preliminary study tested the idea of whether OPA1 and TDP-43 are physically interacting in human platelet derived mitochondria obtained from healthy human subjects.

MeSH terms

  • Amyotrophic Lateral Sclerosis* / metabolism
  • DNA, Mitochondrial / genetics
  • DNA, Mitochondrial / metabolism
  • DNA-Binding Proteins* / genetics
  • DNA-Binding Proteins* / metabolism
  • GTP Phosphohydrolases* / genetics
  • GTP Phosphohydrolases* / metabolism
  • Humans
  • Mitochondria / genetics
  • Mitochondria / metabolism
  • Neurodegenerative Diseases* / metabolism
  • Protein Isoforms / metabolism

Substances

  • DNA, Mitochondrial
  • DNA-Binding Proteins
  • Protein Isoforms
  • TARDBP protein, human
  • OPA1 protein, human
  • GTP Phosphohydrolases