Evidence map›Paper›PMID 22460713›Full record

ArticleAmerican journal of physiology. Cell physiology2012

Chemokine-like receptor 1 regulates skeletal muscle cell myogenesis.

Mark E Issa, Shanmugam Muruganandan, Matthew C Ernst, Sebastian D Parlee, Brian A Zabel, Eugene C Butcher, Christopher J Sinal, Kerry B Goralski

Abstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

20 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. The Role of Selected Proteins in the Pathogenesis of Psoriasis.International journal of molecular sciences · 2025
    Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Chemerin regulates formation and function of brown adipose tissue: Ablation results in increased insulin resistance with high fat challenge and aging.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  11. Article
  12. Effects of conditioned media from murine lung cancer cells and human tumor cells on cultured myotubes.American journal of physiology. Endocrinology and metabolism · 2020
    Article
  13. Article
  14. Review
  15. Article
  16. Chemerin as an independent predictor of cardiovascular event risk.Therapeutic advances in endocrinology and metabolism · 2016
    Review
  17. Article
  18. Chemerin regulation and role in host defense.American journal of clinical and experimental immunology · 2014
    Review
  19. Article
  20. 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

8 authors at 3 institutions in 2 countries.

Mark E IssaFaculty of Health Professions, College of Pharmacy, Dalhousie University, Halifax, Nova Scotia, Canada.
Shanmugam Muruganandan
Matthew C Ernst
Sebastian D Parlee
Brian A Zabel
Eugene C Butcher
Christopher J Sinal
Kerry B Goralski
Dalhousie University · CAPalo Alto Institute · USStanford University · US

Funding

Molecular and Functional Characterization of Chemerin ReceptorsR01AI079320 · NIAID · PALO ALTO VETERANS INSTIT FOR RESEARCH · PI ZABEL, BRIAN A. · 2009 to 2013
$1.7M
CIHRNIAID NIH HHS AI-079320NIAID NIH HHS R01 AI079320
6 · The paper itself

Abstract

The chemokine-like receptor-1 (CMKLR1) is a G protein-coupled receptor that is activated by chemerin, a secreted plasma leukocyte attractant and adipokine. Previous studies identified that CMKLR1 is expressed in skeletal muscle in a stage-specific fashion during embryogenesis and in adult mice; however, its function in skeletal muscle remains unclear. Based on the established function of CMKLR1 in cell migration and differentiation, we investigated the hypothesis that CMKLR1 regulates the differentiation of myoblasts into myotubes. In C(2)C(12) mouse myoblasts, CMKLR1 expression increased threefold with differentiation into multinucleated myotubes. Decreasing CMKLR1 expression by adenoviral-delivered small-hairpin RNA (shRNA) impaired the differentiation of C(2)C(12) myoblasts into mature myotubes and reduced the mRNA expression of myogenic regulatory factors myogenin and MyoD while increasing Myf5 and Mrf4. At embryonic day 12.5 (E12.5), CMKLR1 knockout (CMKLR1(-/-)) mice appeared developmentally delayed and displayed significantly lower wet weights and a considerably diminished myotomal component of somites as revealed by immunolocalization of myosin heavy chain protein compared with wild-type (CMKLR1(+/+)) mouse embryos. These changes were associated with increased Myf5 and decreased MyoD protein expression in the somites of E12.5 CMKLR1(-/-) mouse embryos. Adult male CMKLR1(-/-) mice had significantly reduced bone-free lean mass and weighed less than the CMKLR1(+/+) mice. We conclude that CMKLR1 is essential for myogenic differentiation of C(2)C(12) cells in vitro, and the CMKLR1 null mice have a subtle skeletal muscle deficit beginning from embryonic life that persists during postnatal life.

Indexed as

Muscle DevelopmentAbsorptiometry, PhotonAnimalsCell DifferentiationCells, CulturedMaleMiceMice, KnockoutMuscle CellsMuscle Fibers, SkeletalMuscle ProteinsMuscle, SkeletalMyoD ProteinMyogenic Regulatory Factor 5Myogenic Regulatory FactorsReceptors, ChemokineCMKLR1 protein, mouseMuscle ProteinsMyf5 protein, mouseMyoD Proteinmyogenic factor 6Myogenic Regulatory Factor 5Myogenic Regulatory FactorsReceptors, ChemokineReceptors, G-Protein-CoupledRNA, MessengerRNA, Small Interfering

Identifiers

PMID22460713
PMCPMC3378017
OpenAlexW2015261338

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.