Evidence map›Paper›PMID 34363758›Full record

ArticleDevelopmental cell2021

Proliferative stem cells maintain quiescence of their niche by secreting the Activin inhibitor Follistatin.

Salvador C Herrera, Diego Sainz de la Maza, Lydia Grmai, Shally Margolis, Rebecca Plessel, Michael Burel, Michael O'Connor, Marc Amoyel, Erika A Bach

Open access · bronzeAbstract read
In one paragraph

Article in Developmental cell, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

23 citing papers in PubMed, 38 citations in OpenAlex.

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  11. International journal of molecular sciences · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 3 countries.

Salvador C HerreraBiochemistry and Molecular Pharmacology, NYU Grossman School of Medicine, New York, NY 10016, USA; Centro Andaluz de Biología del Desarrollo, CSIC/Universidad Pablo de Olavide/JA, Carretera de Utrera km 1, 41013 Sevilla, Spain.
Diego Sainz de la MazaDepartment of Cell and Developmental Biology, University College London, Gower Street, London WC1E 6BT, UK.
Lydia GrmaiBiochemistry and Molecular Pharmacology, NYU Grossman School of Medicine, New York, NY 10016, USA.
Shally MargolisBiochemistry and Molecular Pharmacology, NYU Grossman School of Medicine, New York, NY 10016, USA.
Rebecca PlesselBiochemistry and Molecular Pharmacology, NYU Grossman School of Medicine, New York, NY 10016, USA.
Michael BurelBiochemistry and Molecular Pharmacology, NYU Grossman School of Medicine, New York, NY 10016, USA.
Michael O'ConnorDepartment of Genetics, Cell Biology and Development, University of Minnesota, Minneapolis, MN 55455, USA.
Marc AmoyelDepartment of Cell and Developmental Biology, University College London, Gower Street, London WC1E 6BT, UK. Electronic address: marc.amoyel@ucl.ac.uk.
Erika A BachBiochemistry and Molecular Pharmacology, NYU Grossman School of Medicine, New York, NY 10016, USA. Electronic address: erika.bach@nyu.edu.
New York University · USUniversity College London · GBUniversity of Minnesota · US

Funding

Eludicating the Molecular Mechanisms That Regulate Stem Cell Numbers in VivoR01GM085075 · NIGMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BACH, ERIKA A · 2009 to 2023
$4.3M
Training in Pharmacological SciencesT32GM066704 · NIGMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BACH, ERIKA A · 2004 to 2018
$2.6M
Medical Research Council MR/P009646/1Medical Research Council MR/P009646/2NIGMS NIH HHS R01 GM085075NIGMS NIH HHS T32 GM066704
6 · The paper itself

Abstract

Aging causes stem cell dysfunction as a result of extrinsic and intrinsic changes. Decreased function of the stem cell niche is an important contributor to this dysfunction. We use the Drosophila testis to investigate what factors maintain niche cells. The testis niche comprises quiescent "hub" cells and supports two mitotic stem cell pools: germline stem cells and somatic cyst stem cells (CySCs). We identify the cell-cycle-responsive Dp/E2f1 transcription factor as a crucial non-autonomous regulator required in CySCs to maintain hub cell quiescence. Dp/E2f1 inhibits local Activin ligands through production of the Activin antagonist Follistatin (Fs). Inactivation of Dp/E2f1 or Fs in CySCs or promoting Activin receptor signaling in hub cells causes transdifferentiation of hub cells into fully functional CySCs. This Activin-dependent communication between CySCs and hub regulates the physiological decay of the niche with age and demonstrates that hub cell quiescence results from signals from surrounding stem cells.

Indexed as

Stem Cell NicheActivinsAnimalsCell ProliferationCell TransdifferentiationDrosophila melanogasterDrosophila ProteinsFollistatinMaleSpermatozoaTestisTranscription FactorsActivinsDrosophila ProteinsE2f1 protein, DrosophilaFollistatinTranscription FactorsActivinagingcyst stem cellDp/E2fDrosophilafertilityFollistatinnichequiescencetestistransdifferentiation

Identifiers

PMID34363758
PMCPMC8387025
OpenAlexW3191194654

What OpenQuestion holds

Textmetadata
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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.