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Sökning: WFRF:(Schneider Daniel) > (2020-2024) > Demonstration of br...

Demonstration of brain region-specific neuronal vulnerability in human iPSC-based model of familial Parkinson's disease

Brazdis, Razvan Marius (författare)
Friedrich-Alexander University Erlangen-Nürnberg,University Hospital Erlangen
Alecu, Julian E. (författare)
Friedrich-Alexander University Erlangen-Nürnberg
Marsch, Daniel (författare)
Friedrich-Alexander University Erlangen-Nürnberg
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Dahms, Annika (författare)
Friedrich-Alexander University Erlangen-Nürnberg
Simmnacher, Katrin (författare)
Friedrich-Alexander University Erlangen-Nürnberg
Lörentz, Sandra (författare)
Friedrich-Alexander University Erlangen-Nürnberg
Brendler, Anna (författare)
Friedrich-Alexander University Erlangen-Nürnberg
Schneider, Yanni (författare)
University Hospital Erlangen
Marxreiter, Franz (författare)
University Hospital Erlangen
Roybon, Laurent (författare)
Lund University,Lunds universitet,Stamcellslaboratoriet för sjukdomsmodellering i det centrala nervsystemet,Forskargrupper vid Lunds universitet,IPSC Laboratory for CNS Disease Modeling,Lund University Research Groups
Winner, Beate (författare)
Friedrich-Alexander University Erlangen-Nürnberg
Xiang, Wei (författare)
University Hospital Erlangen
Prots, Iryna (författare)
Friedrich-Alexander University Erlangen-Nürnberg
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 (creator_code:org_t)
2020-03-11
2020
Engelska 12 s.
Ingår i: Human Molecular Genetics. - : Oxford University Press (OUP). - 0964-6906 .- 1460-2083. ; 29:7, s. 1180-1191
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Parkinson's disease (PD) is a neurodegenerative disorder characterized by protein inclusions mostly composed of aggregated forms of α-synuclein (α-Syn) and by the progressive degeneration of midbrain dopaminergic neurons (mDANs), resulting in motor symptoms. While other brain regions also undergo pathologic changes in PD, the relevance of α-Syn aggregation for the preferential loss of mDANs in PD pathology is not completely understood yet. To elucidate the mechanisms of the brain region-specific neuronal vulnerability in PD, we modeled human PD using human-induced pluripotent stem cells (iPSCs) from familial PD cases with a duplication (Dupl) of the α-Syn gene (SNCA) locus. Human iPSCs from PD Dupl patients and a control individual were differentiated into mDANs and cortical projection neurons (CPNs). SNCA dosage increase did not influence the differentiation efficiency of mDANs and CPNs. However, elevated α-Syn pathology, as revealed by enhanced α-Syn insolubility and phosphorylation, was determined in PD-derived mDANs compared with PD CPNs. PD-derived mDANs exhibited higher levels of reactive oxygen species and protein nitration levels compared with CPNs, which might underlie elevated α-Syn pathology observed in mDANs. Finally, increased neuronal death was observed in PD-derived mDANs compared to PD CPNs and to control mDANs and CPNs. Our results reveal, for the first time, a higher α-Syn pathology, oxidative stress level, and neuronal death rate in human PD mDANs compared with PD CPNs from the same patient. The finding implies the contribution of pathogenic α-Syn, probably induced by oxidative stress, to selective vulnerability of substantia nigra dopaminergic neurons in human PD.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Neurovetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Neurosciences (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Neurologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Neurology (hsv//eng)

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