Evidence map›Paper›PMID 30423026›Full record

ArticleThe journals of gerontology. Series A, Biological sciences and medical sciences2020

NFκB Regulates Muscle Development and Mitochondrial Function.

Joseph M Valentine, Mengyao E Li, Steven E Shoelson, Ning Zhang, Robert L Reddick, Nicolas Musi

Open access · bronzeAbstract read
In one paragraph

Article in The journals of gerontology. Series A, Biological sciences and medical sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

14 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Molecular hallmarks of ageing in amyotrophic lateral sclerosis.Cellular and molecular life sciences : CMLS · 2024
    Review
  5. Article
  6. Mitochondrial dysfunction: roles in skeletal muscle atrophy.Journal of translational medicine · 2023
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
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

6 authors at 4 institutions in 1 country.

Joseph M ValentineBarshop Institute for Longevity and Aging Studies, University of Texas Health Science Center at San Antonio, Texas.
Mengyao E LiBarshop Institute for Longevity and Aging Studies, University of Texas Health Science Center at San Antonio, Texas.
Steven E ShoelsonJoslin Diabetes Center, Boston, Massachusetts.
Ning ZhangBarshop Institute for Longevity and Aging Studies, University of Texas Health Science Center at San Antonio, Texas.
Robert L ReddickDepartment of Pathology, University of Texas Health Science Center at San Antonio, Texas.
Nicolas MusiBarshop Institute for Longevity and Aging Studies, University of Texas Health Science Center at San Antonio, Texas.
Longevity Biotech (United States) · USThe University of Texas Health Science Center at San Antonio · USJoslin Diabetes Center · USSouth Texas Veterans Health Care System · US

Funding

SPECIAL ASSAY COREP30DK036836 · NIDDK · JOSLIN DIABETES CENTER · PI ROHIT N. KULKARNI · 1986 to 2026
$50.5M
TRANSGENIC COREP30AG013319 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI JAMES FLOYD NELSON · 1995 to 2026
$30.6M
San Antonio OAIC - Research Education Component (REC)P30AG044271 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Adam Salmon · 2015 to 2026
$14.1M
TRAINING GRANT ON THE BIOLOGY OF AGINGT32AG021890 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Erzsebet Kokovay, JAMES FLOYD NELSON · 2003 to 2026
$11.4M
Role of TLR4 on insulin resistance in humansR01DK080157 · NIDDK · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI MUSI, NICOLAS · 2008 to 2017
$3.0M
Effect of age on glucose and lipid metabolismR01DK089229 · NIDDK · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI MUSI, NICOLAS · 2010 to 2013
$1.3M
NIA NIH HHS P30 AG013319NIA NIH HHS P30 AG044271NIA NIH HHS T32 AG021890NIDDK NIH HHS P30 DK036836NIDDK NIH HHS R01 DK080157NIDDK NIH HHS R01 DK089229
6 · The paper itself

Abstract

Nuclear factor (NF)κB is a transcription factor that controls immune and inflammatory signaling pathways. In skeletal muscle, NFκB has been implicated in the regulation of metabolic processes and tissue mass, yet its affects on mitochondrial function in this tissue are unclear. To investigate the role of NFκB on mitochondrial function and its relationship with muscle mass across the life span, we study a mouse model with muscle-specific NFκB suppression (muscle-specific IκBα super-repressor [MISR] mice). In wild-type mice, there was a natural decline in muscle mass with aging that was accompanied by decreased mitochondrial function and mRNA expression of electron transport chain subunits. NFκB inactivation downregulated expression of PPARGC1A, and upregulated TFEB and PPARGC1B. NFκB inactivation also decreased gastrocnemius (but not soleus) muscle mass in early life (1-6 months old). Lower oxygen consumption rates occurred in gastrocnemius and soleus muscles from young MISR mice, whereas soleus (but not gastrocnemius) muscles from old MISR mice displayed increased oxygen consumption compared to age-matched controls. We conclude that the NFκB pathway plays an important role in muscle development and growth. The extent to which NFκB suppression alters mitochondrial function is age dependent and muscle specific. Finally, mitochondrial function and muscle mass are tightly associated in both genotypes and across the life span.

Indexed as

AgingAnimalsCitrate (si)-SynthaseGene Expression Regulation, DevelopmentalMaleMiceMice, Inbred C57BLMice, TransgenicMitochondria, MuscleMuscle DevelopmentMuscle, SkeletalNF-kappa BOxygen ConsumptionSignal TransductionCitrate (si)-SynthaseNF-kappa BInflammationOxygen consumptionROS productionSkeletal muscle

Identifiers

PMID30423026
PMCPMC7328192
OpenAlexW2901089311

What OpenQuestion holds

Textmetadata
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.