Evidence map›Paper›PMID 27091452›Full record

ArticleThe Journal of cell biology2016

Osteopontin ablation ameliorates muscular dystrophy by shifting macrophages to a pro-regenerative phenotype.

Joana Capote, Irina Kramerova, Leonel Martinez, Sylvia Vetrone, Elisabeth R Barton, H Lee Sweeney, M Carrie Miceli, Melissa J Spencer

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 87 papers.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed
8.0field-weighted citation impact, top 2% 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

87 citing papers in PubMed, 123 citations in OpenAlex.

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  9. The Landscape of SPP1Immunology · 2025
    Review
  10. Article
  11. Expansion and pathogenic activation of skeletal muscle-resident macrophages inProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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27 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

8 authors at 2 institutions in 1 country.

Joana CapoteDepartment of Neurology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90095 Molecular, Cellular, and Integrative Physiology Interdepartmental PhD Program, University of California, Los Angeles, Los Angeles, CA 90095.
Irina KramerovaDepartment of Neurology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90095 mspencer@mednet.ucla.edu ikramero@ucla.edu.
Leonel MartinezDepartment of Neurology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90095.
Sylvia VetroneDepartment of Neurology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90095.
Elisabeth R BartonDepartment of Applied Physiology and Kinesiology, University of Florida, Gainesville, FL 32611 Wellstone Muscular Dystrophy Center, University of Florida, Gainesville, FL 32610.
H Lee SweeneyDepartment of Pharmacology and Therapeutics, University of Florida, Gainesville, FL 32610 Wellstone Muscular Dystrophy Center, University of Florida, Gainesville, FL 32610.
M Carrie MiceliDepartment of Microbiology, Immunology, and Molecular Genetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90095 Center for Duchenne Muscular Dystrophy at UCLA, Los Angeles, CA 90095 Wellstone Muscular Dystrophy Center, University of Florida, Gainesville, FL 32610.
Melissa J SpencerDepartment of Neurology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90095 Center for Duchenne Muscular Dystrophy at UCLA, Los Angeles, CA 90095 Wellstone Muscular Dystrophy Center, University of Florida, Gainesville, FL 32610 mspencer@mednet.ucla.edu ikramero@ucla.edu.
University of California, Los Angeles · USUniversity of Florida · US

Funding

Women's CancersP30CA016042 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Samuel Wheeler French · 1985 to 2026
$134.5M
Virology CoreP30AI028697 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KITCHEN, SCOTT G · 1991 to 2018
$39.9M
Using social networks to map and evaluate team science across CTSA hubsUL1TR001427 · NCATS · UNIVERSITY OF FLORIDA · PI MITCHELL, DUANE A. · 2015 to 2024
$37.2M
Training and education CoreU54AR052646 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI MCNALLY, ELIZABETH M, SWEENEY, H LEE · 2005 to 2020
$24.1M
UCLA Muscular Dystrophy Core CenterP30AR057230 · NIAMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SPENCER, MELISSA JAN · 2009 to 2018
$6.2M
Muscle Cell Biology, Pathophysiology, and TherapeuticsT32AR065972 · NIAMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Rachelle Hope Crosbie, THOMAS A. RANDO · 2016 to 2026
$3.9M
THERAPEUTIC APPROACHES FOR MUSCULAR DYSTROPHYR01AR046911 · NIAMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SPENCER, MELISSA JAN · 2000 to 2006
$2.3M
NCATS NIH HHS UL1 TR001427NCI NIH HHS P30 CA016042NIAID NIH HHS HHSN272201300006CNIAID NIH HHS P30 AI028697NIAMS NIH HHS P30 AR057230NIAMS NIH HHS R01 AR046911NIAMS NIH HHS T32 AR065972NIAMS NIH HHS U54 AR052646
6 · The paper itself

Abstract

In the degenerative disease Duchenne muscular dystrophy, inflammatory cells enter muscles in response to repetitive muscle damage. Immune factors are required for muscle regeneration, but chronic inflammation creates a profibrotic milieu that exacerbates disease progression. Osteopontin (OPN) is an immunomodulator highly expressed in dystrophic muscles. Ablation of OPN correlates with reduced fibrosis and improved muscle strength as well as reduced natural killer T (NKT) cell counts. Here, we demonstrate that the improved dystrophic phenotype observed with OPN ablation does not result from reductions in NKT cells. OPN ablation skews macrophage polarization toward a pro-regenerative phenotype by reducing M1 and M2a and increasing M2c subsets. These changes are associated with increased expression of pro-regenerative factors insulin-like growth factor 1, leukemia inhibitory factor, and urokinase-type plasminogen activator. Furthermore, altered macrophage polarization correlated with increases in muscle weight and muscle fiber diameter, resulting in long-term improvements in muscle strength and function in mdx mice. These findings suggest that OPN ablation promotes muscle repair via macrophage secretion of pro-myogenic growth factors.

Indexed as

AnimalsCell PolarityMacrophagesMiceMice, Inbred C57BLMice, KnockoutMusclesMuscular Dystrophy, AnimalNatural Killer T-CellsOsteopontinPhenotypeRegenerationOsteopontin

Identifiers

PMID27091452
PMCPMC5084275
OpenAlexW2337139774

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.