Evidence map›Paper›PMID 30485360›Full record

ArticlePloS one2018

Severe-combined immunodeficient rats can be used to generate a model of perinatal hypoxic-ischemic brain injury to facilitate studies of engrafted human neural stem cells.

Stephanie R Beldick, James Hong, Svetlana Altamentova, Mohamad Khazaei, Anisha Hundal, Mohammad-Masoud Zavvarian, Prakasham Rumajogee, Jonathon Chio, Michael G Fehlings

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. 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
4.0field-weighted citation impact, top 6% 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, 16 citations in OpenAlex.

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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

9 authors at 2 institutions in 1 country.

Stephanie R BeldickInstitute of Medical Science, University of Toronto, Toronto, Ontario, Canada.
James HongInstitute of Medical Science, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0002-5383-8267
Svetlana AltamentovaDivision of Genetics and Development, Krembil Research Institute, Toronto, Ontario, Canada.
Mohamad KhazaeiDivision of Genetics and Development, Krembil Research Institute, Toronto, Ontario, Canada.
Anisha HundalLife Sciences Program, University of Toronto Mississauga, Mississauga, Ontario, Canada.
Mohammad-Masoud ZavvarianInstitute of Medical Science, University of Toronto, Toronto, Ontario, Canada.
Prakasham RumajogeeDivision of Genetics and Development, Krembil Research Institute, Toronto, Ontario, Canada.
Jonathon ChioInstitute of Medical Science, University of Toronto, Toronto, Ontario, Canada.
Michael G FehlingsInstitute of Medical Science, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0002-5722-6364
University of Toronto · CAKrembil Foundation · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cerebral palsy (CP) encompasses a group of non-progressive brain disorders that are often acquired through perinatal hypoxic-ischemic (HI) brain injury. Injury leads to a cascade of cell death events, resulting in lifetime motor and cognitive deficits. There are currently no treatments that can repair the resulting brain damage and improve functional outcomes. To date, preclinical research using neural precursor cell (NPC) transplantation as a therapy for HI brain injury has shown promise. To translate this treatment to the clinic, it is essential that human-derived NPCs also be tested in animal models, however, a major limitation is the high risk of xenograft rejection. A solution is to transplant the cells into immune-deficient rodents, but there are currently no models of HI brain injury established in such a cohort of animals. Here, we demonstrate that a model of HI brain injury can be generated in immune-deficient Prkdc knockout (KO) rats. Long-term deficits in sensorimotor function were similar between KO and wildtype (WT) rats. Interestingly, some aspects of the injury were more severe in KO rats. Additionally, human induced pluripotent stem cell derived (hiPSC)-NPCs had higher survival at 10 weeks post-transplant in KO rats when compared to their WT counterparts. This work establishes a reliable model of neonatal HI brain injury in Prkdc KO rats that will allow for future transplantation, survival, and long-term evaluation of the safety and efficacy of hiPSC-NPCs for neonatal brain damage. This model will enable critical preclinical translational research using human NPCs.

Indexed as

Disease Models, AnimalAnimalsAnimals, NewbornBrainCell SurvivalDNA-Activated Protein KinaseGliosisHumansHypoxia-Ischemia, BrainInduced Pluripotent Stem CellsNeural Stem CellsNuclear ProteinsRandom AllocationRats, Long-EvansRats, TransgenicSevere Combined ImmunodeficiencyDNA-Activated Protein KinaseNuclear ProteinsPrkdc protein, rat

Identifiers

PMID30485360
PMCPMC6261629
OpenAlexW2902137174

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.