Evidence map›Paper›PMID 35844058›Full record

ArticleThe Journal of physiology2022

Leptin mediates the regulation of muscle mass and strength by adipose tissue.

Kelsey H Collins, Chang Gui, Erica V Ely, Kristin L Lenz, Charles A Harris, Farshid Guilak, Gretchen A Meyer

Open access · hybridAbstract read
In one paragraph

Article in The Journal of physiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
5.2field-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

33 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
  2. Review
  3. Sustained loss ofbioRxiv : the preprint server for biology · 2026
    Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Ablation of UCP-1+ cells impacts FAP dynamics in muscle regeneration.American journal of physiology. Cell physiology · 2025
    Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Kelsey H CollinsDepartment of Orthopaedic Surgery, Washington University in St. Louis, MO, USA.
Chang GuiDepartment of Biomedical Engineering, Washington University in St. Louis, MO, USA.
Erica V ElyDepartment of Orthopaedic Surgery, Washington University in St. Louis, MO, USA.
Kristin L LenzDepartment of Orthopaedic Surgery, Washington University in St. Louis, MO, USA.
Charles A HarrisDivision of Endocrinology, Metabolism & Lipid Research, Washington University, St Louis, Missouri, USA.
Farshid GuilakDepartment of Orthopaedic Surgery, Washington University in St. Louis, MO, USA.
Gretchen A MeyerDepartment of Orthopaedic Surgery, Washington University in St. Louis, MO, USA.ORCID 0000-0001-9268-3993
Washington University in St. Louis · US

Funding

Washington University Nutrition Obesity Research CenterP30DK056341 · NIDDK · WASHINGTON UNIVERSITY · PI Brian N Finck · 1999 to 2026
$30.2M
DIABETES &RELATED METABOLIC DISEASEST32DK007120 · NIDDK · WASHINGTON UNIVERSITY · PI MARCO COLONNA, Maria Sara Remedi · 1986 to 2026
$15.7M
VISCOELASTIC PROPERTIES OF NORMAL AND OA CHONDRONSR01AG015768 · NIA · WASHINGTON UNIVERSITY · PI GUILAK, FARSHID · 1998 to 2022
$7.7M
Washington University Rheumatic DiseasesResearch Resource-based CenterP30AR073752 · NIAMS · WASHINGTON UNIVERSITY · PI Deborah J Lenschow, Christine T. Pham · 2018 to 2026
$7.6M
Resource Based Center for Musculoskeletal Biology and Medicine (Overall Application)P30AR074992 · NIAMS · WASHINGTON UNIVERSITY · PI MATTHEW J SILVA · 2019 to 2026
$6.8M
OBESITY, BIOMECHANICS, AND INFLAMMATION IN OSTEOARTHRITISR01AG046927 · NIA · WASHINGTON UNIVERSITY · PI GUILAK, FARSHID · 2013 to 2023
$3.2M
Deconstructing Cartilage Mechanotransduction by Piezo ChannelsR01AR072999 · NIAMS · WASHINGTON UNIVERSITY · PI GUILAK, FARSHID · 2020 to 2024
$2.9M
Promoting Muscle Regeneration through Adipose SignalingR01AR075773 · NIAMS · WASHINGTON UNIVERSITY · PI MEYER, GRETCHEN A · 2019 to 2023
$1.7M
Imaging, Modeling and Engineering of Diabetic TissuesT32DK108742 · NIDDK · WASHINGTON UNIVERSITY · PI NICHOLS, COLIN G · 2016 to 2020
$1.4M
The Role of Fat in OsteoarthritisR00AR078949 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI COLLINS, KELSEY HELEN-MARIE · 2023 to 2025
$715k
Fat-Muscle Cross-Talk in the Injured Rotator CuffR21AR071582 · NIAMS · WASHINGTON UNIVERSITY · PI MEYER, GRETCHEN A · 2018 to 2019
$378k
The Role of Fat in OsteoarthritisK99AR078949 · NIAMS · WASHINGTON UNIVERSITY · PI COLLINS, KELSEY HELEN-MARIE · 2022 to 2023
$98k
NIAMS NIH HHS K99 AR078949NIAMS NIH HHS P30 AR073752NIAMS NIH HHS P30 AR074992NIAMS NIH HHS R00 AR078949NIAMS NIH HHS R01 AR072999NIAMS NIH HHS R01 AR075773NIAMS NIH HHS R21 AR071582NIA NIH HHS R01 AG015768NIA NIH HHS R01 AG046927NIDDK NIH HHS P30 DK056341NIDDK NIH HHS T32 DK007120NIDDK NIH HHS T32 DK108742
6 · The paper itself

Abstract

Adipose tissue secretes numerous cytokines (termed 'adipokines') that have known or hypothesized actions on skeletal muscle. The majority of adipokines have been implicated in the pathological link between excess adipose and muscle insulin resistance, but approximately half also have documented in vitro effects on myogenesis and/or hypertrophy. This complexity suggests a potential dual role for adipokines in the regulation of muscle mass in homeostasis and the development of pathology. In this study, we used lipodystrophic 'fat-free' mice to demonstrate that adipose tissue is indeed necessary for the development of normal muscle mass and strength. Fat-free mice had significantly reduced mass (∼15%) and peak contractile tension (∼20%) of fast-twitch muscles, a slowing of contractile dynamics and decreased cross-sectional area of fast twitch fibres compared to wild-type littermates. These deficits in mass and contractile tension were fully rescued by reconstitution of ∼10% of normal adipose mass, indicating that this phenotype is the direct consequence of absent adipose. We then showed that the rescue is solely mediated by the adipokine leptin, as similar reconstitution of adipose from leptin-knockout mice fails to rescue mass or strength. Together, these data indicate that the development of muscle mass and strength in wild-type mice is dependent on adipose-secreted leptin. This finding extends our current understanding of the multiple roles of adipokines in physiology as well as disease pathophysiology to include a critical role for the adipokine leptin in muscle homeostasis. KEY POINTS: Adipose-derived cytokines (adipokines) have long been implicated in the pathogenesis of insulin resistance in obesity but likely have other under-appreciated roles in muscle physiology. Here we use a fat-free mouse to show that adipose tissue is necessary for the normal development of muscle mass and strength. Through add-back of genetically modified adipose tissue we show that leptin is the key adipokine mediating this regulation. This expands our understanding of leptin's role in adipose-muscle signalling to include development and homeostasis and adds the surprising finding that leptin is the sole mediator of the maintenance of muscle mass and strength by adipose tissue.

Indexed as

Insulin ResistanceLeptinAdipokinesAdipose TissueAnimalsCytokinesMiceMuscle, SkeletalAdipokinesCytokinesLeptinadipokinesanabolicfat-muscle cross-talkmuscle contraction

Identifiers

PMID35844058
PMCPMC9378542
OpenAlexW4285731511

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.