Evidence map›Paper›PMID 25763840›Full record

ArticlePloS one2015

Functional integration of human neural precursor cells in mouse cortex.

Fu-Wen Zhou, Jeff M Fortin, Huan-Xin Chen, Hildabelis Martinez-Diaz, Lung-Ji Chang, Brent A Reynolds, Steven N Roper

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Emerging technologies and ethics-exogenic chimeric humanized organs.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2022
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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

7 authors at 1 institution in 1 country.

Fu-Wen ZhouDepartment of Neurosurgery and the McKnight Brain Institute, University of Florida, Gainesville, Florida, United States of America.
Jeff M FortinDepartment of Neurosurgery and the McKnight Brain Institute, University of Florida, Gainesville, Florida, United States of America.
Huan-Xin ChenDepartment of Neurosurgery and the McKnight Brain Institute, University of Florida, Gainesville, Florida, United States of America.
Hildabelis Martinez-DiazDepartment of Neurosurgery and the McKnight Brain Institute, University of Florida, Gainesville, Florida, United States of America.
Lung-Ji ChangDepartment of Molecular Genetics and Microbiology, University of Florida, Gainesville, Florida, United States of America.
Brent A ReynoldsDepartment of Neurosurgery and the McKnight Brain Institute, University of Florida, Gainesville, Florida, United States of America.
Steven N RoperDepartment of Neurosurgery and the McKnight Brain Institute, University of Florida, Gainesville, Florida, United States of America.
University of Florida · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study investigates the electrophysiological properties and functional integration of different phenotypes of transplanted human neural precursor cells (hNPCs) in immunodeficient NSG mice. Postnatal day 2 mice received unilateral injections of 100,000 GFP+ hNPCs into the right parietal cortex. Eight weeks after transplantation, 1.21% of transplanted hNPCs survived. In these hNPCs, parvalbumin (PV)-, calretinin (CR)-, somatostatin (SS)-positive inhibitory interneurons and excitatory pyramidal neurons were confirmed electrophysiologically and histologically. All GFP+ hNPCs were immunoreactive with anti-human specific nuclear protein. The proportions of PV-, CR-, and SS-positive cells among GFP+ cells were 35.5%, 15.7%, and 17.1%, respectively; around 15% of GFP+ cells were identified as pyramidal neurons. Those electrophysiologically and histological identified GFP+ hNPCs were shown to fire action potentials with the appropriate firing patterns for different classes of neurons and to display spontaneous excitatory and inhibitory postsynaptic currents (sEPSCs and sIPSCs). The amplitude, frequency and kinetic properties of sEPSCs and sIPSCs in different types of hNPCs were comparable to host cells of the same type. In conclusion, GFP+ hNPCs produce neurons that are competent to integrate functionally into host neocortical neuronal networks. This provides promising data on the potential for hNPCs to serve as therapeutic agents in neurological diseases with abnormal neuronal circuitry such as epilepsy.

Indexed as

AnimalsCell SurvivalFetusHeterograftsHumansMiceNeocortexNeural Stem CellsNeuronsTelencephalon

Identifiers

PMID25763840
PMCPMC4357458
OpenAlexW2015433401

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.