Evidence map›Paper›PMID 31417360›Full record

ArticleFrontiers in cellular neuroscience2019

Distinct Vulnerability and Resilience of Human Neuroprogenitor Subtypes in Cerebral Organoid Model of Prenatal Hypoxic Injury.

Nicolas Daviaud, Clément Chevalier, Roland H Friedel, Hongyan Zou

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular neuroscience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
10.9field-weighted citation impact, top 2% 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

34 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Advances in three-dimensional modeling of ischemic injury.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2026
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Brain organoids for hypoxic-ischemic studies: from bench to bedside.Cellular and molecular life sciences : CMLS · 2023
    Review
  12. Review
  13. Neural cortical organoids from self-assembling human iPSC as a model to investigate neurotoxicity in brain ischemia.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2023
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Superoxide dismutase isozymes in cerebral organoids from autism spectrum disorder patients.Journal of neural transmission (Vienna, Austria : 1996) · 2022
    Article
  20. Review
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

4 authors at 3 institutions in 2 countries.

Nicolas DaviaudNash Family Department of Neuroscience, Friedman Brain Institute, New York, NY, United States.
Clément ChevalierThe Center for Microscopy and Molecular Imaging, Université Libre de Bruxelles, Brussels, Belgium.
Roland H FriedelNash Family Department of Neuroscience, Friedman Brain Institute, New York, NY, United States.
Hongyan ZouNash Family Department of Neuroscience, Friedman Brain Institute, New York, NY, United States.
Icahn School of Medicine at Mount Sinai · USAllen Institute for Brain Science · USUniversité Libre de Bruxelles · BE

Funding

Promoting axon regeneration by activation of the Smad1 signaling pathwayR01NS073596 · NINDS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI ZOU, HONGYAN JENNY · 2011 to 2015
$1.7M
Promoting Axon regeneration in Spinal Cord Injury by Epigenetic ModulationR56NS073596 · NINDS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI ZOU, HONGYAN JENNY · 2017 to 2017
$431k
NINDS NIH HHS R01 NS073596NINDS NIH HHS R56 NS073596
6 · The paper itself

Abstract

Prenatal hypoxic injury (HI) is a leading cause of neurological disability. The immediate and long-term effects of hypoxia on progenitor homeostasis and developmental progression during early human brain development remain unclear. This gap is due to difficulty to access human fetal brain tissues and inadequate animal models to study human corticogenesis. Recent optimizations of cerebral organoid models derived from human embryonic stem (ES) cells present new opportunities to investigate pathophysiology of prenatal HI. Here, we implemented a transient HI model using human cerebral organoids with dorsal forebrain specification. We demonstrated that transient hypoxia resulted in immediate and prolonged apoptosis in cerebral organoids, with outer radial glia (oRG), a progenitor population more prominent in primates, and differentiating neuroblasts/immature neurons suffering larger losses. In contrast, neural stem cells in ventricular zone displayed relative resilience to HI and exhibited a shift of cleavage plane angle favoring symmetric division, thereby providing a mechanism to replenish the stem cell pool. Furthermore, we defined the vulnerable window and neurodifferentiation stages that are particularly sensitive to HI. Understanding cell type-specific and stage-dependent effects of prenatal HI on survival and mitotic behavior of human neuroprogenitor subtypes during early human corticogenesis helps elucidate the etiology of neurodevelopmental disorders, and provides a therapeutic starting point to protect the vulnerable populations at critical timeframes.

Indexed as

cerebral organoidshuman corticogenesisneural stem cellneuroprogenitorouter radial gliaprenatal hypoxic injury

Identifiers

PMID31417360
PMCPMC6682705
OpenAlexW2962145716

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.