Evidence map›Paper›PMID 31820346›Full record

ArticleJournal of molecular neuroscience : MN2020

Parkinson's Disease-Associated Changes in the Expression of Neurotrophic Factors and their Receptors upon Neuronal Differentiation of Human Induced Pluripotent Stem Cells.

E V Novosadova, V V Nenasheva, I V Makarova, O V Dolotov, L S Inozemtseva, E L Arsenyeva, S V Chernyshenko, R I Sultanov, S N Illarioshkin, I A Grivennikov and 1 more

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In one paragraph

Article in Journal of molecular neuroscience : MN, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.3field-weighted citation impact, top 45% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 15 citations in OpenAlex.

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  5. Transcription ofJournal of developmental biology · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 1 country.

E V NovosadovaInstitute of Molecular Genetics, Russian Academy of Sciences, Moscow, Russia.
V V NenashevaInstitute of Molecular Genetics, Russian Academy of Sciences, Moscow, Russia. nenasheva@img.ras.ru.ORCID http://orcid.org/0000-0003-3985-6466
I V MakarovaInstitute of Molecular Genetics, Russian Academy of Sciences, Moscow, Russia.
O V DolotovInstitute of Molecular Genetics, Russian Academy of Sciences, Moscow, Russia.
L S InozemtsevaInstitute of Molecular Genetics, Russian Academy of Sciences, Moscow, Russia.
E L ArsenyevaInstitute of Molecular Genetics, Russian Academy of Sciences, Moscow, Russia.
S V ChernyshenkoMoscow State Region University, Moscow, Russia.
R I SultanovFederal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency, Moscow, Russia.
S N IllarioshkinResearch Center of Neurology, Moscow, Russia.
I A GrivennikovInstitute of Molecular Genetics, Russian Academy of Sciences, Moscow, Russia.
V Z TarantulInstitute of Molecular Genetics, Russian Academy of Sciences, Moscow, Russia.
Institute of Molecular Genetics · RUFederal Medical-Biological Agency · RUMoscow Region State University · RUResearch Center of Neurology · RU

Funding

Russian Academy of Sciences 01201356275Российский Фонд Фундаментальных Исследований (РФФИ) 17-29-06008Российский Фонд Фундаментальных Исследований (РФФИ) 19-29-04080
6 · The paper itself

Abstract

Parkinson's disease (PD) is a neurodegenerative pathology resulting from the degeneration of dopaminergic (DA) neurons in the substantia nigra (SN). Neurotrophic factors (NTFs) and their receptors are key regulators of the survival, differentiation, and development of neurons. However, the role of these factors in the pathogenesis of PD is still unclear. Here, we analyzed the expression of NTFs and their receptors in human induced pluripotent stem cells (iPSCs) derived from the fibroblasts of patients with PD and healthy donors (HDs). Four PD-derived iPSC lines with different mutations and three cell lines from HDs at different stages of neuronal differentiation were used for RT-qPCR analysis and ELISA. We found that the mRNA levels of most analyzed genes were altered in PD-derived cells compared with those in HD-derived cells at all stages. Importantly, irrespective of PD-associated mutations, the mRNA levels of the BDNF and GDNF genes were mostly increased or unchanged in predominantly DA terminally differentiated neurons (TDNs) compared with those in HD-derived cells. Strikingly, in contrast to BDNF and GDNF mRNA levels, BDNF and GDNF protein levels were lower in almost all PD-derived TDNs than in HD-derived cells, thus indicating the dysregulation of NTF expression at the post-transcriptional level. We suggest that this dysregulation is one of the important signs of PD development.

Indexed as

Brain-Derived Neurotrophic FactorCell LineCells, CulturedDopaminergic NeuronsGlial Cell Line-Derived Neurotrophic FactorHumansInduced Pluripotent Stem CellsMutationNeurogenesisParkinson DiseaseReceptor, trkBRNA, MessengerBrain-Derived Neurotrophic FactorGlial Cell Line-Derived Neurotrophic FactorReceptor, trkBRNA, MessengerInduced pluripotent stem cellsNeuronal differentiationNeurotrophic factorsParkinson’s diseaseReceptors

Identifiers

PMID31820346
OpenAlexW2994311353

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.