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DOI 10.3390/ijms25137278

Медицинская библиотека · International journal of molecular sciences · 2024

Targeting Macrophage Polarization for Reinstating Homeostasis following Tissue Damage.

Du Qiran, Dickinson Anna, Nakuleswaran Pruthvi, Maghami Susan, Alagoda Savindu, Hook Andrew L, Ghaemmaghami Amir M

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Аннотация

Tissue regeneration and remodeling involve many complex stages. Macrophages are critical in maintaining micro-environmental homeostasis by regulating inflammation and orchestrating wound healing. They display high plasticity in response to various stimuli, showing a spectrum of functional phenotypes that vary from M1 (pro-inflammatory) to M2 (anti-inflammatory) macrophages. While transient inflammation is an essential trigger for tissue healing following an injury, sustained inflammation (e.g., in foreign body response to implants, diabetes or inflammatory diseases) can hinder tissue healing and cause tissue damage. Modulating macrophage polarization has emerged as an effective strategy for enhancing immune-mediated tissue regeneration and promoting better integration of implantable materials in the host. This article provides an overview of macrophages' functional properties followed by discussing different strategies for modulating macrophage polarization. Advances in the use of synthetic and natural biomaterials to fabricate immune-modulatory materials are highlighted. This reveals that the development and clinical application of more effective immunomodulatory systems targeting macrophage polarization under pathological conditions will be driven by a detailed understanding of the factors that regulate macrophage polarization and biological function in order to optimize existing methods and generate novel strategies to control cell phenotype.

Для цитирования: Du Qiran, Dickinson Anna, Nakuleswaran Pruthvi, Maghami Susan, Alagoda Savindu, Hook Andrew L, Ghaemmaghami Amir M. Targeting Macrophage Polarization for Reinstating Homeostasis following Tissue Damage.. International journal of molecular sciences. 2024. DOI: 10.3390/ijms25137278.

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