Evidence map›Paper›PMID 33243288›Full record

ArticleSkeletal muscle2020

Tetraspanin CD82 is necessary for muscle stem cell activation and supports dystrophic muscle function.

Arielle Hall, Tatiana Fontelonga, Alec Wright, Katlynn Bugda Gwilt, Jeffrey Widrick, Alessandra Pasut, Francesco Villa, Cynthia K Miranti, Devin Gibbs, Evan Jiang and 3 more

Open access · goldAbstract read
In one paragraph

Article in Skeletal muscle, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

12 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Building Haplotype-Resolved 3D Genome Maps of Chicken Skeletal Muscle.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Lysine methyltransferase 2D regulates muscle fiber size and muscle cell differentiation.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  12. Review
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

13 authors at 5 institutions in 2 countries.

Arielle HallDivision of Genetics and Genomics, Boston Children's Hospital, Boston, MA, 02115, USA.
Tatiana FontelongaDivision of Genetics and Genomics, Boston Children's Hospital, Boston, MA, 02115, USA.
Alec WrightDivision of Genetics and Genomics, Boston Children's Hospital, Boston, MA, 02115, USA.
Katlynn Bugda GwiltDivision of Gastroenterology, Hepatology and Nutrition, Boston Children's Hospital, Boston, MA, 02115, USA.
Jeffrey WidrickDivision of Genetics and Genomics, Boston Children's Hospital, Boston, MA, 02115, USA.
Alessandra PasutLaboratory of Angiogenesis and Vascular metabolism, Center for Cancer Biology, VIB and KU Leuven, 3000, Leuven, Belgium.
Francesco VillaF.M. Kirby Neurobiology Center, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Cynthia K MirantiDepartment of Cellular and Molecular Medicine, University of Arizona College of Medicine, Tucson, AZ, 85724, USA.
Devin GibbsMolecular Biology Institute, UCLA, Los Angeles, CA, 90095, USA.
Evan JiangThe University of Pennsylvania, College of Arts and Sciences, Philadelphia, PA, 19104, USA.
Hui MengDepartment of Pathology and Laboratory Medicine and Neuroscience Research Center, Medical College of Wisconsin, Milwaukee, WI, 53226, USA.
Michael W LawlorDepartment of Pathology and Laboratory Medicine and Neuroscience Research Center, Medical College of Wisconsin, Milwaukee, WI, 53226, USA.
Emanuela GussoniDivision of Genetics and Genomics, Boston Children's Hospital, Boston, MA, 02115, USA. Emanuela.gussoni@enders.tch.harvard.edu.ORCID 0000-0002-9915-3677
Boston Children's Hospital · USMedical College of Wisconsin · USUniversity of Arizona · USUniversity of the Sciences · USVIB-KU Leuven Center for Cancer Biology · BE

Funding

Mouse Neurodevelopmental Behavior CoreU54HD090255 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI POMEROY, SCOTT LOREN · 2016 to 2020
$5.2M
Tetraspanin CD82 in muscle satellite cells quiescence and differentiationR01AR069582 · NIAMS · BOSTON CHILDREN'S HOSPITAL · PI GUSSONI, EMANUELA · 2017 to 2022
$1.9M
NIAMS NIH HHS R01 AR069582NICHD NIH HHS U54 HD090255
6 · The paper itself

Abstract

backgroundTetraspanins are a family of proteins known to assemble protein complexes at the cell membrane. They are thought to play diverse cellular functions in tissues by modifying protein-binding partners, thus bringing complexity and diversity in their regulatory networks. Previously, we identified the tetraspanin KAI/CD82 as a prospective marker for human muscle stem cells. CD82 expression appeared decreased in human Duchenne muscular dystrophy (DMD) muscle, suggesting a functional link to muscular dystrophy, yet whether this decrease is a consequence of dystrophic pathology or a compensatory mechanism in an attempt to rescue muscle from degeneration is currently unknown.

methodsWe studied the consequences of loss of CD82 expression in normal and dystrophic skeletal muscle and examined the dysregulation of downstream functions in mice aged up to 1 year.

resultsExpression of CD82 is important to sustain satellite cell activation, as in its absence there is decreased cell proliferation and less efficient repair of injured muscle. Loss of CD82 in dystrophic muscle leads to a worsened phenotype compared to control dystrophic mice, with decreased pulmonary function, myofiber size, and muscle strength. Mechanistically, decreased myofiber size in CD82

conclusionBasal CD82 expression is important to dystrophic muscle, as its loss leads to significantly weakened myofibers and impaired muscle function, accompanied by decreased satellite cell activity that is unable to protect and repair myofiber damage.

Indexed as

AnimalsCell ProliferationCells, CulturedFemaleKangai-1 ProteinMaleMiceMice, Inbred C57BLMuscle StrengthMuscular Dystrophy, DuchenneProto-Oncogene Proteins c-aktPTEN PhosphohydrolaseSatellite Cells, Skeletal MuscleSignal TransductionTOR Serine-Threonine KinasesCd82 antigen, mouseKangai-1 ProteinProto-Oncogene Proteins c-aktPTEN PhosphohydrolaseTOR Serine-Threonine KinasesAKTmTORMuscular dystrophyRegenerationStem cellsTetraspanin

Identifiers

PMID33243288
PMCPMC7693590
OpenAlexW3109839809

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.