Evidence map›Paper›PMID 24859199›Full record

ArticleNature neuroscience2014

ALK5-dependent TGF-β signaling is a major determinant of late-stage adult neurogenesis.

Yingbo He, Hui Zhang, Andrea Yung, Saul A Villeda, Philipp A Jaeger, Oluwatobi Olayiwola, Nina Fainberg, Tony Wyss-Coray

Open access · greenAbstract read
In one paragraph

Article in Nature neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed, 1 pooled it
6.3field-weighted citation impact, top 3% 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

71 citing papers in PubMed, 1 synthesis or guideline pooled it, 98 citations in OpenAlex.

  1. Pooled it
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  10. TSPYL1 as a Critical Regulator of TGFβ Signaling through Repression of TGFBR1 and TSPYL2.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  11. GDF11 and aging biology - controversies resolved and pending.The journal of cardiovascular aging · 2023
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  18. Small molecule C381 targets the lysosome to reduce inflammation and ameliorate disease in models of neurodegeneration.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
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11 more citing papers are in PubMed but not listed here.

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

8 authors at 3 institutions in 1 country.

Yingbo HeDepartment of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, California, USA.
Hui ZhangDepartment of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, California, USA.
Andrea YungDepartment of Biology, Stanford University, Stanford, California, USA.
Saul A VilledaPresent address: The Eli and Edythe Broad Center for Regeneration Medicine and Stem Cell Research, University of California San Francisco, San Francisco, California, USA (S.A.V.), Department of Bioengineering, University of California San Diego, La Jolla, California, USA, and Department of Medicine, University of California San Diego, La Jolla, California, USA (P.A.J.).
Philipp A JaegerPresent address: The Eli and Edythe Broad Center for Regeneration Medicine and Stem Cell Research, University of California San Francisco, San Francisco, California, USA (S.A.V.), Department of Bioengineering, University of California San Diego, La Jolla, California, USA, and Department of Medicine, University of California San Diego, La Jolla, California, USA (P.A.J.).ORCID 0000000236240802
Oluwatobi OlayiwolaDepartment of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, California, USA.
Nina FainbergDepartment of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, California, USA.
Tony Wyss-Coray1] Department of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, California, USA. [2] Center for Tissue Regeneration, Repair and Rehabilitation, VA Palo Alto Health Care System, Palo Alto, California, USA.
Stanford University · USUniversity of California, San Francisco · USVA Palo Alto Health Care System · US

Funding

Training Program in Basic NeuroscienceT32MH020016 · NIMH · STANFORD UNIVERSITY · PI Justin L Gardner, Merritt C Maduke · 1997 to 2026
$16.2M
VECTOR COREP30NS069375 · NINDS · STANFORD UNIVERSITY · PI SHAMLOO, MEHRDAD · 2011 to 2019
$6.3M
TGFbeta signaling in neurodegeneration and Alzhimer'sR01AG027505 · NIA · STANFORD UNIVERSITY · PI WYSS-CORAY, TONY · 2006 to 2010
$1.3M
NIA NIH HHS AG27505NIA NIH HHS R01 AG027505NIMH NIH HHS T32 MH020016NINDS NIH HHS NS069375-01A1NINDS NIH HHS P30 NS069375
6 · The paper itself

Abstract

The transforming growth factor-β (TGF-β) signaling pathway serves critical functions in CNS development, but, apart from its proposed neuroprotective actions, its physiological role in the adult brain is unclear. We observed a prominent activation of TGF-β signaling in the adult dentate gyrus and expression of downstream Smad proteins in this neurogenic zone. Consistent with a function of TGF-β signaling in adult neurogenesis, genetic deletion of the TGF-β receptor ALK5 reduced the number, migration and dendritic arborization of newborn neurons. Conversely, constitutive activation of neuronal ALK5 in forebrain caused a marked increase in these aspects of neurogenesis and was associated with higher expression of c-Fos in newborn neurons and with stronger memory function. Our findings describe an unexpected role for ALK5-dependent TGF-β signaling as a regulator of the late stages of adult hippocampal neurogenesis, which may have implications for changes in neurogenesis during aging and disease.

Indexed as

AnimalsAnimals, NewbornBlotting, WesternConditioning, PsychologicalDentate GyrusDependovirusDoxycyclineFearFemaleGene ExpressionGenetic VectorsHippocampusImmunohistochemistryLuciferasesMaleMemoryDoxycyclineLuciferasesProtein Serine-Threonine KinasesReceptors, Transforming Growth Factor betaReceptor, Transforming Growth Factor-beta Type ITgfbr1 protein, mouseTransforming Growth Factor beta

Identifiers

PMID24859199
PMCPMC4096284
OpenAlexW2093443054

What OpenQuestion holds

Textmetadata
LicenceTDM
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.