Evidence map›Paper›PMID 23967244›Full record

ArticlePloS one2013

TDP-43, an ALS linked protein, regulates fat deposition and glucose homeostasis.

Nancy R Stallings, Krishna Puttaparthi, Katherine J Dowling, Christina M Luther, Dennis K Burns, Kathryn Davis, Jeffrey L Elliott

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed, 1 pooled it
3.7field-weighted citation impact, top 7% 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

64 citing papers in PubMed, 1 synthesis or guideline pooled it, 96 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. TDP-43: unveiling the hidden key to cellular fate decisions.Cell communication and signaling : CCS · 2025
    Review
  5. Article
  6. Article
  7. CRISPR/Cas9-MediatedAnimals : an open access journal from MDPI · 2025
    Article
  8. Article
  9. Article
  10. Chchd10: A Novel Metabolic Sensor Modulating Adipose Tissue Homeostasis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  11. Skeletal muscle disorders as risk factors for type 2 diabetes.Molecular and cellular endocrinology · 2025
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Implications of TDP-43 in non-neuronal systems.Cell communication and signaling : CCS · 2023
    Review
  20. Skeletal muscle in amyotrophic lateral sclerosis.Brain : a journal of neurology · 2023
    Review

4 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

7 authors at 3 institutions in 1 country.

Nancy R StallingsDepartment of Neurology and Neurotherapeutics, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Krishna Puttaparthi
Katherine J Dowling
Christina M Luther
Dennis K Burns
Kathryn Davis
Jeffrey L Elliott
The University of Texas Southwestern Medical Center · USNanotherapeutics (United States) · USTexas Plastic Surgery · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The identification of proteins which determine fat and lean body mass composition is critical to better understanding and treating human obesity. TDP-43 is a well-conserved RNA-binding protein known to regulate alternative splicing and recently implicated in the pathogenesis of amyotrophic lateral sclerosis (ALS). While TDP-43 knockout mice show early embryonic lethality, post-natal conditional knockout mice show weight loss, fat depletion, and rapid death, suggesting an important role for TDP-43 in regulating energy metabolism. Here we report, that over-expression of TDP-43 in transgenic mice can result in a phenotype characterized by increased fat deposition and adipocyte hypertrophy. In addition, TDP-43 over-expression in skeletal muscle results in increased steady state levels of Tbc1d1, a RAB-GTPase activating protein involved in Glucose 4 transporter (Glut4) translocation. Skeletal muscle fibers isolated from TDP-43 transgenic mice show altered Glut4 translocation in response to insulin and impaired insulin mediated glucose uptake. These results indicate that levels of TDP-43 regulate body fat composition and glucose homeostasis in vivo.

Indexed as

AdiposityHomeostasisAdipose TissueAnimalsDNA-Binding ProteinsGene ExpressionGlucoseGlucose Transporter Type 4GTPase-Activating ProteinsHumansInsulinMaleMiceMice, TransgenicMuscle, SkeletalNuclear ProteinsDNA-Binding ProteinsGlucoseGlucose Transporter Type 4GTPase-Activating ProteinsInsulinNuclear ProteinsTbc1d1 protein, mouse

Identifiers

PMID23967244
PMCPMC3742534
OpenAlexW2038300433

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.