Evidence map›Paper›PMID 28207192›Full record

ArticleStem cells (Dayton, Ohio)2017

Temporal-Spatial Establishment of Initial Niche for the Primary Spermatogonial Stem Cell Formation Is Determined by an ARID4B Regulatory Network.

Ray-Chang Wu, Yang Zeng, Yu-Fang Chen, Rainer B Lanz, Mei-Yi Wu

Abstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2017. 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
–field-weighted citation impact
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.

  1. Review
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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

5 authors.

Ray-Chang WuDepartment of Biochemistry and Molecular Medicine, The George Washington University, Washington, District of Columbia, USA.
Yang ZengDepartment of Biochemistry and Molecular Medicine, The George Washington University, Washington, District of Columbia, USA.
Yu-Fang ChenDepartment of Biochemistry and Molecular Medicine, The George Washington University, Washington, District of Columbia, USA.
Rainer B LanzDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas, USA.
Mei-Yi WuDepartment of Biochemistry and Molecular Medicine, The George Washington University, Washington, District of Columbia, USA.ORCID 0000-0002-0183-976X

Funding

Corepressor Function of Steroid Receptor Coactivator-3 in Breast CancerR01CA188471 · NCI · GEORGE WASHINGTON UNIVERSITY · PI WU, RAY-CHANG · 2015 to 2019
$1.8M
Steroid receptor coactivator-3 and cancer stem cellsR21CA187857 · NCI · GEORGE WASHINGTON UNIVERSITY · PI WU, RAY-CHANG · 2014 to 2015
$379k
NCI NIH HHS R01 CA188471NCI NIH HHS R21 CA187857
6 · The paper itself

Abstract

During neonatal testis development, centrally located gonocytes migrate to basement membrane of the seminiferous cords, where physical contact with a niche established by Sertoli cells is essential for transition of gonocytes into spermatogonial stem cells (SSCs). To provide structural support and signaling stimuli for the gonocyte-to-SSC transition that occurs at a specific location during a finite phase, temporal-spatial establishment of the niche is critical. To date, the factors that guide Sertoli cells to establish the initial stem cell niche remain largely unknown. Using the Sertoli cell-specific Arid4b knockout (Arid4bSCKO) mice, we demonstrated that ablation of AT-rich interaction domain 4B (ARID4B) resulted in abnormal detachment of Sertoli cells from the basement membrane of seminiferous cords during the gonocyte-to-SSC transition phase, suggesting failure to establish a niche for the SSC formation. Without support by a niche environment, gonocytes showed disarranged cell distribution in the Arid4bSCKO testes and underwent apoptosis. The commitment of gonocytes to differentiate into the spermatogonial lineage was broken and the capability of SSCs to self-renew and differentiate was also impaired. Gene expression profiling revealed the molecular mechanisms responsible for the phenotypic changes in the Arid4bSCKO testes, by identifying genes important for stem cell niche function as downstream effectors of ARID4B, including genes that encode gap junction protein alpha-1, KIT ligand, anti-Müllerian hormone, Glial cell-line derived neurotrophic factor, inhibin alpha, inhibin beta, and cytochrome P450 family 26 subfamily b polypeptide 1. Our results identified ARID4B as a master regulator of a signaling network that governs the establishment of a niche during the critical gonocyte-to-SSC transition phase to control the fate of gonocytes and SSCs. Stem Cells 2017;35:1554-1565.

Indexed as

Gene Regulatory NetworksStem Cell NicheAnimalsAnimals, NewbornApoptosisCell DifferentiationCell LineageCell Self RenewalDNA-Binding ProteinsDown-RegulationGene Expression Regulation, DevelopmentalGlial Cell Line-Derived Neurotrophic FactorMaleMice, Inbred C57BLMice, KnockoutOrgan SpecificityDNA-Binding ProteinsGlial Cell Line-Derived Neurotrophic FactorRbbp1l1 protein, mouseAT-rich interaction domain 4BGonocyteSertoli cellSpermatogoniaSpermatogonial stem cell niche

Identifiers

PMID28207192
PMCPMC5743547

What OpenQuestion holds

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Registered trials

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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.