» Articles » PMID: 34335621

The Role of Macrophages During Mammalian Tissue Remodeling and Regeneration Under Infectious and Non-Infectious Conditions

Overview
Journal Front Immunol
Date 2021 Aug 2
PMID 34335621
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

Several infectious pathologies in humans, such as tuberculosis or SARS-CoV-2, are responsible for tissue or lung damage, requiring regeneration. The regenerative capacity of adult mammals is limited to few organs. Critical injuries of non-regenerative organs trigger a repair process that leads to a definitive architectural and functional disruption, while superficial wounds result in scar formation. Tissue lesions in mammals, commonly studied under non-infectious conditions, trigger cell death at the site of the injury, as well as the production of danger signals favouring the massive recruitment of immune cells, particularly macrophages. Macrophages are also of paramount importance in infected injuries, characterized by the presence of pathogenic microorganisms, where they must respond to both infection and tissue damage. In this review, we compare the processes implicated in the tissue repair of non-infected infected injuries of two organs, the skeletal muscles and the lungs, focusing on the primary role of macrophages. We discuss also the negative impact of infection on the macrophage responses and the possible routes of investigation for new regenerative therapies to improve the recovery state as seen with COVID-19 patients.

Citing Articles

Tissue macrophages: origin, heterogenity, biological functions, diseases and therapeutic targets.

Guan F, Wang R, Yi Z, Luo P, Liu W, Xie Y Signal Transduct Target Ther. 2025; 10(1):93.

PMID: 40055311 PMC: 11889221. DOI: 10.1038/s41392-025-02124-y.


Origin, Function, and Implications of Intestinal and Hepatic Macrophages in the Pathogenesis of Alcohol-Associated Liver Disease.

Hu Y, Schnabl B, Starkel P Cells. 2025; 14(3).

PMID: 39936998 PMC: 11816606. DOI: 10.3390/cells14030207.


The effect of intrauterine growth restriction on the developing pancreatic immune system.

Golden T, Garifallou J, Conine C, Simmons R bioRxiv. 2024; .

PMID: 39386426 PMC: 11463653. DOI: 10.1101/2024.09.19.613902.


Interaction among inflammasome, PANoptosise, and innate immune cells in infection of influenza virus: Updated review.

Wei L, Wang X, Zhou H Immun Inflamm Dis. 2023; 11(9):e997.

PMID: 37773712 PMC: 10521376. DOI: 10.1002/iid3.997.


Acute immune responses in zebrafish and evasive behavior of a parasite - who is winning?.

Mathiessen H, Kjeldgaard-Nintemann S, Gonzalez C, Henard C, Reimer J, Gelskov S Front Cell Infect Microbiol. 2023; 13:1190931.

PMID: 37475962 PMC: 10354369. DOI: 10.3389/fcimb.2023.1190931.


References
1.
Unkel B, Hoegner K, Clausen B, Lewe-Schlosser P, Bodner J, Gattenloehner S . Alveolar epithelial cells orchestrate DC function in murine viral pneumonia. J Clin Invest. 2012; 122(10):3652-64. PMC: 3461909. DOI: 10.1172/JCI62139. View

2.
Karin M, Clevers H . Reparative inflammation takes charge of tissue regeneration. Nature. 2016; 529(7586):307-15. PMC: 5228603. DOI: 10.1038/nature17039. View

3.
Leppkes M, Schick M, Hohberger B, Mahajan A, Knopf J, Schett G . Updates on NET formation in health and disease. Semin Arthritis Rheum. 2019; 49(3S):S43-S48. DOI: 10.1016/j.semarthrit.2019.09.011. View

4.
Tan S, Krasnow M . Developmental origin of lung macrophage diversity. Development. 2016; 143(8):1318-27. PMC: 4852511. DOI: 10.1242/dev.129122. View

5.
Cakarova L, Marsh L, Wilhelm J, Mayer K, Grimminger F, Seeger W . Macrophage tumor necrosis factor-alpha induces epithelial expression of granulocyte-macrophage colony-stimulating factor: impact on alveolar epithelial repair. Am J Respir Crit Care Med. 2009; 180(6):521-32. DOI: 10.1164/rccm.200812-1837OC. View