International Journal of Molecular Sciences (Jan 2022)

Analysis of mRNA and Protein Levels of <i>CAP2</i>, <i>DLG1</i> and <i>ADAM10</i> Genes in Post-Mortem Brain of Schizophrenia, Parkinson’s and Alzheimer’s Disease Patients

  • Anna Di Maio,
  • Arianna De Rosa,
  • Silvia Pelucchi,
  • Martina Garofalo,
  • Benedetta Marciano,
  • Tommaso Nuzzo,
  • Fabrizio Gardoni,
  • Andrea M. Isidori,
  • Monica Di Luca,
  • Francesco Errico,
  • Andrea De Bartolomeis,
  • Elena Marcello,
  • Alessandro Usiello

DOI
https://doi.org/10.3390/ijms23031539
Journal volume & issue
Vol. 23, no. 3
p. 1539

Abstract

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Schizophrenia (SCZ) is a mental illness characterized by aberrant synaptic plasticity and connectivity. A large bulk of evidence suggests genetic and functional links between postsynaptic abnormalities and SCZ. Here, we performed quantitative PCR and Western blotting analysis in the dorsolateral prefrontal cortex (DLPFC) and hippocampus of SCZ patients to investigate the mRNA and protein expression of three key spine shapers: the actin-binding protein cyclase-associated protein 2 (CAP2), the sheddase a disintegrin and metalloproteinase 10 (ADAM10), and the synapse-associated protein 97 (SAP97). Our analysis of the SCZ post-mortem brain indicated increased DLG1 mRNA in DLPFC and decreased CAP2 mRNA in the hippocampus of SCZ patients, compared to non-psychiatric control subjects, while the ADAM10 transcript was unaffected. Conversely, no differences in CAP2, SAP97, and ADAM10 protein levels were detected between SCZ and control individuals in both brain regions. To assess whether DLG1 and CAP2 transcript alterations were selective for SCZ, we also measured their expression in the superior frontal gyrus of patients affected by neurodegenerative disorders, like Parkinson’s and Alzheimer’s disease. Interestingly, also in Parkinson’s disease patients, we found a selective reduction of CAP2 mRNA levels relative to controls but unaltered protein levels. Taken together, we reported for the first time altered CAP2 expression in the brain of patients with psychiatric and neurological disorders, thus suggesting that aberrant expression of this gene may contribute to synaptic dysfunction in these neuropathologies.

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