Evidence map›Paper›PMID 28575744›Full record

ArticleRedox biology2017

Decreased neural precursor cell pool in NADPH oxidase 2-deficiency: From mouse brain to neural differentiation of patient derived iPSC.

Zeynab Nayernia, Marilena Colaianna, Natalia Robledinos-Antón, Eveline Gutzwiller, Frédérique Sloan-Béna, Elisavet Stathaki, Yousef Hibaoui, Antonio Cuadrado, Jürgen Hescheler, Marie-José Stasia and 3 more

Open access · goldAbstract read
In one paragraph

Article in Redox biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

14 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Nerve Growth Factor and Autoimmune Diseases.Current issues in molecular biology · 2023
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. ROS Live Cell Imaging During Neuronal Development.Journal of visualized experiments : JoVE · 2021
    Article
  10. Review
  11. Article
  12. Review
  13. nox2/cybb Deficiency Affects Zebrafish Retinotectal Connectivity.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  14. Article
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

13 authors at 6 institutions in 4 countries.

Zeynab NayerniaDepartment of Pathology and Immunology, University of Geneva Medical School, 1-rue Michel Servet, 1211 Geneva, Switzerland.
Marilena ColaiannaDepartment of Pathology and Immunology, University of Geneva Medical School, 1-rue Michel Servet, 1211 Geneva, Switzerland.
Natalia Robledinos-AntónInstituto de Investigaciones Biomédicas "Alberto Sols", Faculty of Medicine, Autonomous University of Madrid (UAM), Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Madrid, Spain.
Eveline GutzwillerDepartment of Pathology and Immunology, University of Geneva Medical School, 1-rue Michel Servet, 1211 Geneva, Switzerland.
Frédérique Sloan-BénaHôpitaux Universitaires de Genève HUG, Laboratoires de Cytogénétique Constitutionnelle, Service de Médecine Génétique, Geneva, Switzerland.
Elisavet StathakiHôpitaux Universitaires de Genève HUG, Laboratoires de Cytogénétique Constitutionnelle, Service de Médecine Génétique, Geneva, Switzerland.
Yousef HibaouiDepartment of Genetic Medicine and Development, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland.
Antonio CuadradoInstituto de Investigaciones Biomédicas "Alberto Sols", Faculty of Medicine, Autonomous University of Madrid (UAM), Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Madrid, Spain.
Jürgen HeschelerCenter for Physiology and Pathophysiology, Institute for Neurophysiology, Medical Faculty, University of Cologne, Cologne 50931, Germany.
Marie-José StasiaUniversité Grenoble Alpes, Techniques de l'Ingénierie Médicale et de la Complexité- Grenoble, F38000 Grenoble, France.
Tomo SaricCenter for Physiology and Pathophysiology, Institute for Neurophysiology, Medical Faculty, University of Cologne, Cologne 50931, Germany.
Vincent JaquetDepartment of Pathology and Immunology, University of Geneva Medical School, 1-rue Michel Servet, 1211 Geneva, Switzerland.
Karl-Heinz KrauseDepartment of Pathology and Immunology, University of Geneva Medical School, 1-rue Michel Servet, 1211 Geneva, Switzerland. Electronic address: Karl-Heinz.Krause@unige.ch.
University of Geneva · CHHôpital Beau-Séjour · CHUniversity of Cologne · DEBiomedical Research Networking Center on Neurodegenerative Diseases · ESInstituto de Investigaciones Biomédicas Sols-Morreale · ESTranslational Innovation in Medicine and Complexity · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is emerging evidence for the involvement of reactive oxygen species (ROS) in the regulation of stem cells and cellular differentiation. Absence of the ROS-generating NADPH oxidase NOX2 in chronic granulomatous disease (CGD) patients, predominantly manifests as immune deficiency, but has also been associated with decreased cognition. Here, we investigate the role of NOX enzymes in neuronal homeostasis in adult mouse brain and in neural cells derived from human induced pluripotent stem cells (iPSC). High levels of NOX2 were found in mouse adult neurogenic regions. In NOX2-deficient mice, neurogenic regions showed diminished redox modifications, as well as decrease in neuroprecursor numbers and in expression of genes involved in neural differentiation including NES, BDNF and OTX2. iPSC from healthy subjects and patients with CGD were used to study the role of NOX2 in human in vitro neuronal development. Expression of NOX2 was low in undifferentiated iPSC, upregulated upon neural induction, and disappeared during neuronal differentiation. In human neurospheres, NOX2 protein and ROS generation were polarized within the inner cell layer of rosette structures. NOX2 deficiency in CGD-iPSCs resulted in an abnormal neural induction in vitro, as revealed by a reduced expression of neuroprogenitor markers (NES, BDNF, OTX2, NRSF/REST), and a decreased generation of mature neurons. Vector-mediated NOX2 expression in NOX2-deficient iPSCs rescued neurogenesis. Taken together, our study provides novel evidence for a regulatory role of NOX2 during early stages of neurogenesis in mouse and human.

Indexed as

NeurogenesisAnimalsBrainBrain-Derived Neurotrophic FactorCells, CulturedGranulomatous Disease, ChronicHumansInduced Pluripotent Stem CellsMiceNADPH Oxidase 2NestinNeural Stem CellsOtx Transcription FactorsRE1-Silencing Transcription FactorReactive Oxygen SpeciesRepressor ProteinsBrain-Derived Neurotrophic FactorCybb protein, mouseNADPH Oxidase 2Nes protein, mouseNestinOtx2 protein, mouseOtx Transcription FactorsRE1-Silencing Transcription FactorReactive Oxygen SpeciesRepressor ProteinsAdult neurogenesisInduced pluripotent stem cells (iPSC)in vitro neural differentiationNeural stem/progenitor cellsNOX2Reactive oxygen species

Identifiers

PMID28575744
PMCPMC5454143
OpenAlexW2609801639

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.