Evidence map›Paper›PMID 36376495›Full record

ArticleExperimental & molecular medicine2022

Induction of Nanog in neural progenitor cells for adaptive regeneration of ischemic brain.

Gyung-Ah Jung, Jin-A Kim, Hwan-Woo Park, Hyemi Lee, Mi-Sook Chang, Kyung-Ok Cho, Byeong-Wook Song, Hyun-Ju Kim, Yunhee Kim Kwon, Il-Hoan Oh

Open access · goldAbstract read
In one paragraph

Article in Experimental & molecular medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

7 citing papers in PubMed, 9 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

10 authors at 7 institutions in 2 countries.

Gyung-Ah Jung *Catholic High-Performance Cell Therapy Center & Department of Medical Life Science, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Jin-A Kim *Catholic High-Performance Cell Therapy Center & Department of Medical Life Science, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Hwan-Woo ParkDepartment of Oral Anatomy, Dental Research Institute & School of Dentistry, Seoul National University, Seoul, Korea.ORCID 0000-0001-8029-2004
Hyemi LeeDepartment of Biomedical and Pharmaceutical Sciences, Kyung Hee University, Seoul, Korea.
Mi-Sook ChangDepartment of Oral Anatomy, Dental Research Institute & School of Dentistry, Seoul National University, Seoul, Korea.ORCID 0000-0002-4379-204X
Kyung-Ok ChoDepartment of Pharmacology, Department of Biomedicine & Health Sciences, Catholic Neuroscience Institute, Institute of Aging and Metabolic Diseases, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID 0000-0002-1314-7584
Byeong-Wook SongCollege of Medicine, Institute for Bio-Medical Convergence, Catholic Kwandong University, Gangneung-si, 25601, Korea.
Hyun-Ju KimDepartment of Biomedical and Pharmaceutical Sciences, Kyung Hee University, Seoul, Korea. kimhyunzoo@gmail.com.
Yunhee Kim KwonDepartment of Biomedical and Pharmaceutical Sciences, Kyung Hee University, Seoul, Korea. kimhy@khu.ac.kr.
Il-Hoan OhCatholic High-Performance Cell Therapy Center & Department of Medical Life Science, College of Medicine, The Catholic University of Korea, Seoul, Korea. iho@catholic.ac.kr.
Catholic University of Korea · KRKyung Hee University · KRCatholic Kwandong University · KRKonyang University · KRKyung Hee Cyber University · KRRegenerative Medicine Institute · MXSeoul National University Dental Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

NANOG plays a key role in cellular plasticity and the acquisition of the stem cell state during reprogramming, but its role in the regenerative process remains unclear. Here, we show that the induction of NANOG in neuronal cells is necessary for the physiological initiation of neuronal regeneration in response to ischemic stress. Specifically, we found that NANOG was preferentially expressed in undifferentiated neuronal cells, and forced expression of Nanog in neural progenitor cells (NPCs) promoted their self-renewing expansion both in ex-vivo slice cultures and in vitro limiting dilution analysis. Notably, the upstream region of the Nanog gene contains sequence motifs for hypoxia-inducible factor-1 alpha (HIF-1α). Therefore, cerebral neurons exposed to hypoxia significantly upregulated NANOG expression selectively in primitive (CD133

Indexed as

Nanog Homeobox ProteinNeural Stem CellsAnimalsBrainHypoxiaNeurogenesisNeuronsNanog Homeobox Protein

Identifiers

PMID36376495
PMCPMC9722910
OpenAlexW4308948116

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.