Evidence mapPaperPMID 39092292Full record

ReviewMedComm2024

Macrophage plasticity: signaling pathways, tissue repair, and regeneration.

Lingfeng Yan, Jue Wang, Xin Cai, Yih-Cherng Liou, Han-Ming Shen, Jianlei Hao, Canhua Huang, Gaoxing Luo, Weifeng He

Abstract readReview
In one paragraph

Review in MedComm, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 183 papers.

0numbers the graph read from it
0cells of the map it votes in
183citing 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

183 citing papers in PubMed.

  1. Gut microbes · 2026
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123 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

9 authors.

Lingfeng YanInstitute of Burn Research State Key Laboratory of Trauma and Chemical Poisoning the First Affiliated Hospital of Army Medical University (the Third Military Medical University) Chongqing China.ORCID https://orcid.org/0009-0002-4997-0780
Jue WangInstitute of Burn Research State Key Laboratory of Trauma and Chemical Poisoning the First Affiliated Hospital of Army Medical University (the Third Military Medical University) Chongqing China.
Xin CaiInstitute of Burn Research State Key Laboratory of Trauma and Chemical Poisoning the First Affiliated Hospital of Army Medical University (the Third Military Medical University) Chongqing China.
Yih-Cherng LiouDepartment of Biological Sciences Faculty of Science National University of Singapore Singapore Singapore.
Han-Ming ShenFaculty of Health Sciences University of Macau Macau China.
Jianlei HaoGuangdong Provincial Key Laboratory of Tumor Interventional Diagnosis and Treatment Zhuhai Institute of Translational Medicine Zhuhai People's Hospital (Zhuhai Clinical Medical College of Jinan University) Jinan University Zhuhai Guangdong China.
Canhua HuangState Key Laboratory of Biotherapy and Cancer Center West China Hospital and West China School of Basic Medical Sciences and Forensic Medicine Sichuan University, and Collaborative Innovation Center for Biotherapy Chengdu China.
Gaoxing LuoInstitute of Burn Research State Key Laboratory of Trauma and Chemical Poisoning the First Affiliated Hospital of Army Medical University (the Third Military Medical University) Chongqing China.
Weifeng HeInstitute of Burn Research State Key Laboratory of Trauma and Chemical Poisoning the First Affiliated Hospital of Army Medical University (the Third Military Medical University) Chongqing China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Macrophages are versatile immune cells with remarkable plasticity, enabling them to adapt to diverse tissue microenvironments and perform various functions. Traditionally categorized into classically activated (M1) and alternatively activated (M2) phenotypes, recent advances have revealed a spectrum of macrophage activation states that extend beyond this dichotomy. The complex interplay of signaling pathways, transcriptional regulators, and epigenetic modifications orchestrates macrophage polarization, allowing them to respond to various stimuli dynamically. Here, we provide a comprehensive overview of the signaling cascades governing macrophage plasticity, focusing on the roles of Toll-like receptors, signal transducer and activator of transcription proteins, nuclear receptors, and microRNAs. We also discuss the emerging concepts of macrophage metabolic reprogramming and trained immunity, contributing to their functional adaptability. Macrophage plasticity plays a pivotal role in tissue repair and regeneration, with macrophages coordinating inflammation, angiogenesis, and matrix remodeling to restore tissue homeostasis. By harnessing the potential of macrophage plasticity, novel therapeutic strategies targeting macrophage polarization could be developed for various diseases, including chronic wounds, fibrotic disorders, and inflammatory conditions. Ultimately, a deeper understanding of the molecular mechanisms underpinning macrophage plasticity will pave the way for innovative regenerative medicine and tissue engineering approaches.

Indexed as

epigenetic regulationmacrophagesplasticitysignaling pathwaystissue repair

Identifiers

PMID39092292
PMCPMC11292402

What Socratic 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 Socratic graph.