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Macrophage Polarization: A Novel Target and Strategy for Pathological Scarring.
Wang, Xinyi; Liu, Dewu.
Affiliation
  • Wang X; Medical Center of Burn Plastic and Wound Repair, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, 17 Yongwaizheng Street, Nanchang, 330006, Jiangxi, People's Republic of China.
  • Liu D; Queen Mary Academy, Nanchang University, Nanchang, Jiangxi, People's Republic of China.
Tissue Eng Regen Med ; 2024 Oct 01.
Article in En | MEDLINE | ID: mdl-39352458
ABSTRACT

BACKGROUND:

Abnormal scarring imposes considerable challenges and burdens on the lives of patients and healthcare system. Macrophages at the wound site are found to be of great concern to overall wound healing. There have been many studies indicating an inextricably link between dysfunctional macrophages and fibrotic scars. Macrophages are not only related to pathogen destruction and phagocytosis of apoptotic cells, but also involved in angiogenesis, keratinization and collagen deposition. These abundant cell functions are attributed to specific heterogeneity and plasticity of macrophages, which also add an extra layer of complexity to correlational researches.

METHODS:

This article summarizes current understanding of macrophage polarization in scar formation and several prevention and treatment strategies on pathological scarring related to regulation of macrophage behaviors by utilizing databases such as PubMed, Google Scholar and so on.

RESULTS:

There are many studies proving that macrophages participate in the course of wound healing by converting their predominant phenotype. The potential of macrophages in managing hypertrophic scars and keloid lesions have been underscored.

CONCLUSION:

Macrophage polarization offers new prevention strategies for pathological scarringLearning about and targeting at macrophages may be helpful in achieving optimum wound healing.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Tissue Eng Regen Med Year: 2024 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Tissue Eng Regen Med Year: 2024 Document type: Article Country of publication: