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Genes Implicated in Familial Parkinson's Disease Provide a Dual Picture of Nigral Dopaminergic Neurodegeneration with Mitochondria Taking Center Stage

期刊

出版社

MDPI
DOI: 10.3390/ijms22094643

关键词

mitochondria; vesicular transport; mitophagy; Lewy bodies; synuclein aggregation; familial Parkinson’ s disease; early-onset Parkinson’ s disease

资金

  1. Spanish Ministerio de Ciencia, Innovacion y Universidades (MCIU) [RTI2018-09204-B-I00]
  2. Spanish Agencia Estatal de Investigacion (AEI) [RTI2018-09204-B-I00]
  3. UE FEDER funds

向作者/读者索取更多资源

This paper explores the potential mechanisms of dopaminergic denervation in Parkinson's disease by studying genes related to familial cases. It proposes that gene mutations can alter the processing of alpha-synuclein or disrupt vesicular trafficking and protein processing mechanisms. Mitochondria play a central role in both pathways, suggesting that targeting G protein-coupled receptors in neurons' mitochondria may lead to new therapeutic approaches.
The mechanism of nigral dopaminergic neuronal degeneration in Parkinson's disease (PD) is unknown. One of the pathological characteristics of the disease is the deposition of alpha-synuclein (alpha-syn) that occurs in the brain from both familial and sporadic PD patients. This paper constitutes a narrative review that takes advantage of information related to genes (SNCA, LRRK2, GBA, UCHL1, VPS35, PRKN, PINK1, ATP13A2, PLA2G6, DNAJC6, SYNJ1, DJ-1/PARK7 and FBXO7) involved in familial cases of Parkinson's disease (PD) to explore their usefulness in deciphering the origin of dopaminergic denervation in many types of PD. Direct or functional interactions between genes or gene products are evaluated using the Search Tool for the Retrieval of Interacting Genes/Proteins (STRING) database. The rationale is to propose a map of the interactions between SNCA, the gene encoding for alpha-syn that aggregates in PD, and other genes, the mutations of which lead to early-onset PD. The map contrasts with the findings obtained using animal models that are the knockout of one of those genes or that express the mutated human gene. From combining in silico data from STRING-based assays with in vitro and in vivo data in transgenic animals, two likely mechanisms appeared: (i) the processing of native alpha-syn is altered due to the mutation of genes involved in vesicular trafficking and protein processing, or (ii) alpha-syn mutants alter the mechanisms necessary for the correct vesicular trafficking and protein processing. Mitochondria are a common denominator since both mechanisms require extra energy production, and the energy for the survival of neurons is obtained mainly from the complete oxidation of glucose. Dopamine itself can result in an additional burden to the mitochondria of dopaminergic neurons because its handling produces free radicals. Drugs acting on G protein-coupled receptors (GPCRs) in the mitochondria of neurons may hopefully end up targeting those receptors to reduce oxidative burden and increase mitochondrial performance. In summary, the analysis of the data of genes related to familial PD provides relevant information on the etiology of sporadic cases and might suggest new therapeutic approaches.

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