Evidence map›Paper›PMID 33810946›Full record

ArticleCytokine2021

Reduced apoptosis of monocytes and macrophages is associated with their persistence in wounds of diabetic mice.

Jingbo Pang, Mark Maienschein-Cline, Timothy J Koh

Open access · greenAbstract read
In one paragraph

Article in Cytokine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

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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

3 authors at 1 institution in 1 country.

Jingbo PangCenter for Wound Healing and Tissue Regeneration, Department of Kinesiology and Nutrition, University of Illinois at Chicago, Chicago, IL 60612, United States.
Mark Maienschein-ClineResearch Informatics Core, University of Illinois at Chicago, Chicago, IL 60612, United States.
Timothy J KohCenter for Wound Healing and Tissue Regeneration, Department of Kinesiology and Nutrition, University of Illinois at Chicago, Chicago, IL 60612, United States. Electronic address: tjkoh@uic.edu.
University of Illinois Chicago · US

Funding

Strengthening Stakeholder Engagement in Human Research Protections.UL1TR002003 · NCATS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI KARNIK, NIRANJAN SUBHASH, MERMELSTEIN, ROBIN J. · 2016 to 2024
$33.7M
Macrophage Phenotypes and Tissue RepairR35GM136228 · NIGMS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI TIMOTHY J KOH · 2020 to 2026
$3.7M
Macrophage Phenotype and Impaired Wound HealingR01GM092850 · NIGMS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI KOH, TIMOTHY J · 2011 to 2019
$3.5M
NCATS NIH HHS UL1 TR002003NIGMS NIH HHS R01 GM092850NIGMS NIH HHS R35 GM136228
6 · The paper itself

Abstract

Monocytes and macrophages (Mo/MΦ) rapidly accumulate in skin wounds after injury, then disappear as healing progresses. However, the mechanisms underlying their ultimate fate in wounds remain to be elucidated. Here, we show that apoptosis of Mo/MΦ parallels their reduction as wound healing progresses in non-diabetic mice. scRNAseq analysis confirmed enriched apoptosis GO pathways on day 6 post-injury in wound Mo/MΦ from non-diabetic mice. In contrast, there was significantly less Mo/MΦ apoptosis in wounds from diabetic mice, particularly in the pro-inflammatory Ly6C+ population, which may contribute to persistent Mo/MΦ accumulation and chronic inflammation. scRNAseq analysis implicated TNF, MAPK, Jak-STAT, and FoxO signaling pathways in promoting wound Mo/MΦ apoptosis in non-diabetic mice while cell proliferation related pathways appeared to be activated in diabetic mice. These novel findings indicate that reduced apoptosis is a contributor to persistent Mo/MΦ accumulation in diabetic wounds. These findings also highlight pathways that may regulate Mo/MΦ apoptosis during wound healing, which could be targeted to help resolve inflammation and improve healing.

Indexed as

ApoptosisWound HealingAnimalsBase SequenceDiabetes Mellitus, ExperimentalDisease Models, AnimalMacrophagesMaleMiceMice, Inbred C57BLMonocytesSingle-Cell AnalysisSkinApoptosisDiabetesInflammationMacrophage and monocyteSingle cell RNA sequencingWound healing

Identifiers

PMID33810946
PMCPMC8043999
OpenAlexW3143274484

What OpenQuestion holds

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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.