Evidence map›Paper›PMID 30148186›Full record

ArticleBio-protocol2018

Immunohistochemical Identification of Human Skeletal Muscle Macrophages.

Kate Kosmac, Bailey D Peck, R Grace Walton, Jyothi Mula, Philip A Kern, Marcas M Bamman, Richard A Dennis, Cale A Jacobs, Christian Lattermann, Darren L Johnson and 1 more

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Bio-protocol, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02261961 (Immune Function and Muscle Adaptations to Resistance Exercise in Older Adults), which is not on this map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
4.3field-weighted citation impact, top 5% 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.

NCT02261961 nacompletednot on this map

Immune Function and Muscle Adaptations to Resistance Exercise in Older Adults

TypeinterventionalSponsorVA Office of Research and DevelopmentRan2014 to 2019Enrolled59ConditionsSarcopenia, Aging, Immune FunctionArmsTDAP, Acute Resistance Exercise, Resistance Exercise Training, Post-training Follow-up, Nutritional Supplement (Muscle Armor)
3 · Its place in the literature

Who cites it

46 citing papers in PubMed, 78 citations in OpenAlex.

  1. Neuromuscular electrical stimulation and protein during bed rest increases CD11bApplied physiology, nutrition, and metabolism = Physiologie appliquee, nutrition et metabolisme · 2020
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  13. Macrophage immunometabolism: emerging targets for regrowth in aging muscle.American journal of physiology. Endocrinology and metabolism · 2025
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  14. Observational
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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

11 authors at 4 institutions in 1 country.

Kate KosmacDepartment of Rehabilitation Sciences, College of Health Sciences and Center for Muscle Biology, University of Kentucky, Lexington, KY, USA.
Bailey D PeckDepartment of Rehabilitation Sciences, College of Health Sciences and Center for Muscle Biology, University of Kentucky, Lexington, KY, USA.
R Grace WaltonDepartment of Rehabilitation Sciences, College of Health Sciences and Center for Muscle Biology, University of Kentucky, Lexington, KY, USA.
Jyothi MulaCenter for Genetic Muscle Disorders, Kennedy Krieger Institute, Baltimore, MD, USA.
Philip A KernDepartment of Internal Medicine, Division of Endocrinology and Center for Clinical and Translational Sciences, University of Kentucky, Lexington, KY, USA.
Marcas M BammanCenter for Exercise Medicine and Department of Cell, Developmental, and Integrative Biology, University of Alabama at Birmingham, Birmingham, AL, USA.
Richard A DennisGeriatric Research Education and Clinical Center, Central Arkansas Veterans Healthcare System, Little Rock, AR, USA.
Cale A JacobsDepartment of Orthopaedic Surgery and Sports Medicine, University of Kentucky, Lexington, KY, USA.
Christian LattermannDepartment of Orthopaedic Surgery and Sports Medicine, University of Kentucky, Lexington, KY, USA.
Darren L JohnsonDepartment of Orthopaedic Surgery and Sports Medicine, University of Kentucky, Lexington, KY, USA.
Charlotte A PetersonDepartment of Rehabilitation Sciences, College of Health Sciences and Center for Muscle Biology, University of Kentucky, Lexington, KY, USA.
University of Kentucky · USGeriatric Research Education and Clinical Center · USKennedy Krieger Institute · USUniversity of Alabama at Birmingham · US

Funding

University of Kentucky Markey Cancer Center Support Grant ECIA SupplementP30CA177558 · NCI · UNIVERSITY OF KENTUCKY · PI KATHLEEN L. O'CONNOR · 2013 to 2026
$38.3M
Kentucky Center for Clinical and Translational ScienceUL1TR001998 · NCATS · UNIVERSITY OF KENTUCKY · PI HARTMANN, KATHERINE E, KERN, PHILIP A · 2016 to 2025
$34.2M
The role of satellite cells in adult skeletal muscle growth and maintenanceR01AR060701 · NIAMS · UNIVERSITY OF KENTUCKY · PI MCCARTHY, JOHN JOSEPH, PETERSON, CHARLOTTE A. · 2010 to 2019
$3.3M
Novel Actions of Metformin to Augment Resistance Training Adaptations in Older AdR01AG046920 · NIA · UNIVERSITY OF KENTUCKY · PI BAMMAN, MARCAS M, KERN, PHILIP A · 2014 to 2018
$2.9M
Immune Function and Muscle Adaptations to Resistance Exercise in Older AdultsI01RX001203 · VA · CENTRAL ARKANSAS VETERANS HLTHCARE SYS · PI DENNIS, RICHARD A. · 2015 to 2018
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NCATS NIH HHS UL1 TR001998NCI NIH HHS P30 CA177558NIAMS NIH HHS R01 AR060701NIA NIH HHS R01 AG046920RRD VA I01 RX001203
6 · The paper itself

Abstract

Macrophages have well-characterized roles in skeletal muscle repair and regeneration. Relatively little is known regarding the role of resident macrophages in skeletal muscle homeostasis, extracellular matrix remodeling, growth, metabolism and adaptation to various stimuli including exercise and training. Despite speculation into macrophage contributions during these processes, studies characterizing macrophages in non-injured muscle are limited and methods used to identify macrophages vary. A standardized method for the identification of human resident skeletal muscle macrophages will aide in the characterization of these immune cells and allow for the comparison of results across studies. Here, we present an immunohistochemistry (IHC) protocol, validated by flow cytometry, to distinctly identify resident human skeletal muscle macrophage populations. We show that CD11b and CD206 double IHC effectively identifies macrophages in human skeletal muscle. Furthermore, the majority of macrophages in non-injured human skeletal muscle show a 'mixed' M1/M2 phenotype, expressing CD11b, CD14, CD68, CD86 and CD206. A relatively small population of CD11b+/CD206- macrophages are present in resting skeletal muscle. Changes in the relative abundance of this population may reflect important changes in the skeletal muscle environment. CD11b and CD206 IHC in muscle also reveals distinct morphological features of macrophages that may be related to the functional status of these cells.

Indexed as

CD11bCD206CD68Flow cytometryImmune cellsImmunohistochemistryMacrophagesSkeletal muscle

Identifiers

PMID30148186
PMCPMC6105281
OpenAlexW2808995499

What OpenQuestion holds

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Registered trials

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.