Evidence map›Paper›PMID 26832401›Full record

ArticleCell reports2016

Inborn Errors of Long-Chain Fatty Acid β-Oxidation Link Neural Stem Cell Self-Renewal to Autism.

Zhigang Xie, Albert Jones, Jude T Deeney, Seong Kwon Hur, Vytas A Bankaitis

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed, 1 pooled it
10.2field-weighted citation impact, top 1% 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

73 citing papers in PubMed, 1 synthesis or guideline pooled it, 122 citations in OpenAlex.

  1. Pooled it
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  7. Observational
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  13. Overexpression of CPT1A disrupts the maintenance and regenerative function of muscle stem cells.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
  14. Brain development and bioenergetic changes.Neurobiology of disease · 2024
    Review
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13 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

5 authors at 3 institutions in 1 country.

Zhigang XieDepartment of Molecular and Cellular Medicine, Texas A&M University Health Science Center, College Station, TX 77843, USA. Electronic address: zxie@tamhsc.edu.
Albert JonesDepartment of Medicine, Obesity Research Center, Boston University School of Medicine, Boston, MA 02118, USA.
Jude T DeeneyDepartment of Medicine, Obesity Research Center, Boston University School of Medicine, Boston, MA 02118, USA.
Seong Kwon HurDepartment of Molecular and Cellular Medicine, Texas A&M University Health Science Center, College Station, TX 77843, USA.
Vytas A BankaitisDepartment of Molecular and Cellular Medicine, Texas A&M University Health Science Center, College Station, TX 77843, USA.
Boston University · USTexas A&M Health Science Center · USTexas A&M University · US

Funding

Transgenic CoreP30DK046200 · NIDDK · TUFTS MEDICAL CENTER · PI CORKEY, BARBARA E. · 1992 to 2021
$25.0M
METABOLIC REGULATION OF INSULIN SECRETIONR01DK035914 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI CORKEY, BARBARA E., SHIRIHAI, ORIAN S · 1986 to 2013
$5.3M
Functional Anatomy of Mammalian Phosphatidylinositol Transfer ProteinsR01GM112591 · NIGMS · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI BANKAITIS, VYTAS A · 2015 to 2018
$1.7M
Role of FMRP and FXR1 in neural stem cells during neocortical developmentR21HD069857 · NICHD · BOSTON UNIVERSITY MEDICAL CAMPUS · PI XIE, ZHIGANG · 2011 to 2012
$450k
NICHD NIH HHS 1R21HD069857NICHD NIH HHS R21 HD069857NIDDK NIH HHS P30 DK046200NIDDK NIH HHS R01 DK035914NIDDK NIH HHS R01DK035914NIGMS NIH HHS R01 GM112591NIGMS NIH HHS R01GM112591
6 · The paper itself

Abstract

Inborn errors of metabolism (IEMs) occur with high incidence in human populations. Especially prevalent among these are inborn deficiencies in fatty acid β-oxidation (FAO), which are clinically associated with developmental neuropsychiatric disorders, including autism. We now report that neural stem cell (NSC)-autonomous insufficiencies in the activity of TMLHE (an autism risk factor that supports long-chain FAO by catalyzing carnitine biosynthesis), of CPT1A (an enzyme required for long-chain FAO transport into mitochondria), or of fatty acid mobilization from lipid droplets reduced NSC pools in the mouse embryonic neocortex. Lineage tracing experiments demonstrated that reduced flux through the FAO pathway potentiated NSC symmetric differentiating divisions at the expense of self-renewing stem cell division modes. The collective data reveal a key role for FAO in controlling NSC-to-IPC transition in the mammalian embryonic brain and suggest NSC self renewal as a cellular mechanism underlying the association between IEMs and autism.

Indexed as

Cell Self Renewal3-Hydroxyacyl CoA DehydrogenasesAcetyl-CoA C-AcyltransferaseAnimalsAutistic DisorderBiocatalysisCarbon-Carbon Double Bond IsomerasesCarnitineCarnitine O-PalmitoyltransferaseCell DivisionCell LineageEnoyl-CoA HydrataseFatty AcidsFemaleLipid DropletsLipid Metabolism, Inborn Errors3-Hydroxyacyl CoA DehydrogenasesAcetyl-CoA C-AcyltransferaseCarbon-Carbon Double Bond IsomerasesCarnitineCarnitine O-PalmitoyltransferaseEnoyl-CoA Hydratasefatty acid oxidation complexFatty AcidsRacemases and EpimerasesRNA, Small Interfering

Identifiers

PMID26832401
PMCPMC4749429
OpenAlexW2270074037

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.