Expression changes of genes associated with apoptosis and survival processes in Parkinson's disease

Neurosci Lett. 2016 Feb 26:615:72-7. doi: 10.1016/j.neulet.2016.01.029. Epub 2016 Jan 22.

Abstract

Parkinson's disease (PD) is a neurodegenerative disorder characterized by progressive degeneration of the dopaminergic neurons in substantia nigra, presumably due to increased apoptosis and oxidative stress. To investigate whether PD-induced survival/apoptosis gene expression changes can serve as prognostic biomarkers of PD, we measured expression levels of phosphatidylinositol-4,5-bisphosphate 3-kinase (PI3K)/Akt pathway factors and additional apoptotic and anti-apoptotic factors in peripheral blood mononuclear cells (PBMC) of PD patients (n=50) and healthy controls (n=50) by real time PCR. Expression levels of apoptotic factors phosphatase and tensin homolog (PTEN) and mitochondrial apoptosis-inducing factor 1 (AIFM1) were significantly decreased, anti-apoptotic factors DJ-1 and Akt-1 were significantly increased and anti-apoptotic Bcl-2 was significantly decreased in PD patients. Expression levels of AIFM1 were significantly correlated with Hoehn-Yahr scores. Moreover, PD patients with postural instability showed significantly reduced expression levels of anti-apoptotic DJ-1, Akt-1 and mTOR than PD patients without postural instability. Expression profiles of brain samples of mice with rotenone-induced PD model and PBMC samples of PD patients showed remarkable resemblance. Our results indicate that the anti-apoptotic PI3K/Akt pathway is over activated in PD, presumably as an effort to compensate for increased neuronal apoptosis and oxidative stress. By contrast, patients with postural instability show reduced anti-apoptotic factor expression suggesting that this compensating mechanism fails in patients with this particular motor symptom. PBMC expression levels of AIFM1 might serve as a biomarker of disability and disease progression in PD.

Keywords: Akt; Apoptosis; Parkinson’s; Real time PCR; Survival; disease.

MeSH terms

  • Aged
  • Animals
  • Apoptosis / genetics*
  • Apoptosis Inducing Factor / metabolism
  • Biomarkers / metabolism
  • Brain / metabolism
  • Case-Control Studies
  • Caspase 3 / metabolism
  • Caspase 9 / metabolism
  • Female
  • Humans
  • Leukocytes, Mononuclear / metabolism
  • Male
  • Mice, Inbred C57BL
  • Middle Aged
  • PTEN Phosphohydrolase / metabolism
  • Parkinson Disease / etiology
  • Parkinson Disease / metabolism*
  • Parkinson Disease / pathology*
  • Phosphatidylinositol 3-Kinases / metabolism
  • Proto-Oncogene Proteins c-akt / metabolism
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Rotenone
  • Signal Transduction

Substances

  • Apoptosis Inducing Factor
  • Biomarkers
  • Proto-Oncogene Proteins c-bcl-2
  • Rotenone
  • Phosphatidylinositol 3-Kinases
  • Proto-Oncogene Proteins c-akt
  • PTEN Phosphohydrolase
  • Pten protein, mouse
  • Caspase 3
  • Caspase 9