Evidence map›Paper›PMID 25678696›Full record

ArticleJournal of applied physiology (Bethesda, Md. : 1985)2015

Anti-inflammatory macrophages improve skeletal muscle recovery from ischemia-reperfusion.

David W Hammers, Viktoriya Rybalko, Melissa Merscham-Banda, Pei-Ling Hsieh, Laura J Suggs, Roger P Farrar

Abstract read
In one paragraph

Article in Journal of applied physiology (Bethesda, Md. : 1985), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–field-weighted citation impact
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

24 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Cell-Inspired Biomaterials for Modulating Inflammation.Tissue engineering. Part B, Reviews · 2022
    Review
  10. Review
  11. Review
  12. Actions and interactions of IGF-I and MMPs during muscle regeneration.Seminars in cell & developmental biology · 2021
    Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Macrophage Regulation of Muscle Regrowth From Disuse in Aging.Exercise and sport sciences reviews · 2019
    Review
  18. Article
  19. Review
  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

6 authors.

David W HammersDepartment of Kinesiology, The University of Texas at Austin, Austin, Texas; and.
Viktoriya RybalkoDepartment of Kinesiology, The University of Texas at Austin, Austin, Texas; and.
Melissa Merscham-BandaDepartment of Kinesiology, The University of Texas at Austin, Austin, Texas; and.
Pei-Ling HsiehDepartment of Kinesiology, The University of Texas at Austin, Austin, Texas; and.
Laura J SuggsDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, Texas.
Roger P FarrarDepartment of Kinesiology, The University of Texas at Austin, Austin, Texas; and rfarrar@austin.utexas.edu.

Funding

Nanotracer Development to Track Stem Cell TherapyR01EB015007 · NIBIB · UNIVERSITY OF TEXAS AT AUSTIN · PI SUGGS, LAURA J · 2012 to 2020
$3.7M
NIBIB NIH HHS 1R01-EB-015007-01NIBIB NIH HHS R01 EB015007
6 · The paper itself

Abstract

The presence of macrophages (MPs) is essential for skeletal muscle to properly regenerate following injury. The aim of this study was the evaluation of MP profiles and their importance in skeletal muscle recovering from tourniquet-induced ischemia-reperfusion (I/R). Using flow cytometry, we identified two distinct CD11b(+) MP populations that differ in expression of the surface markers Ly-6C and F4/80. These populations are prominent at 3 and 5 days of reperfusion and molecularly correspond to inflammatory and anti-inflammatory MP phenotypes. Sorted MP populations demonstrated high levels of IGF-I expression, and whole muscle post-I/R IGF-I expression strongly correlates with F4/80 expression. This suggests MPs largely influence postinjury IGF-I upregulation. We additionally demonstrate that direct intramuscular injection of FACS-isolated CD11b(+)Ly-6C(lo)F4/80(hi) MPs improves the functional and histological recovery of I/R-affected muscle. Taken together, these data further support the substantial influence of the innate immune system on muscle regeneration and suggest MP-focused therapeutic approaches may greatly facilitate skeletal muscle recovery from substantial injury.

Indexed as

AnimalsAntigens, LyCD11b AntigenMacrophagesMaleMice, Inbred C57BLMuscle, SkeletalRecovery of FunctionReperfusion InjuryAntigens, LyCD11b AntigenLy-6C antigen, mouseflow cytometrymacrophagemyogenesisregenerative medicinereperfusion

Identifiers

PMID25678696
PMCPMC4398886

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.