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异位骨化中的巨噬细胞极化:炎症、骨生成及新兴治疗靶点

Macrophage Polarization in Heterotopic Ossification: Inflammation, Osteogenesis, and Emerging Therapeutic Targets.

作者信息

Ren Yifei, Zhao Wenwen, Liu Mengchao, Lin Hui

机构信息

School of Basic Medical Sciences, Jiangxi Medical College, Nanchang University, Nanchang 330006, China.

Queen Mary School, Jiangxi Medical College, Nanchang University, Nanchang 330006, China.

出版信息

Int J Mol Sci. 2025 Jun 17;26(12):5821. doi: 10.3390/ijms26125821.

Abstract

Heterotopic ossification (HO) refers to an abnormal process characterized by the aberrant development of bone within soft tissues, leading to significant impairments in patients' mobility and overall quality of life. Macrophages, as a crucial element of the immune system, are instrumental in the different stages of heterotopic ossification through their dynamic polarization state (pro-inflammatory M1 and anti-inflammatory M2 phenotypes) and secretion of different cytokines. This review explores novel mechanisms of M1 and M2 macrophage-mediated heterotopic ossification, emphasizing the involvement of the inflammatory microenvironment, osteogenic factors, and osteogenic signaling pathways. In addition, we explore promising therapeutic strategies targeting macrophage polarization and function, including agents that modulate the inflammatory microenvironment, such as IL-1 inhibitors, parovastatin, and metformin, as well as agents that affect macrophage osteogenic signaling, such as TGF-βRII-Fc, Galunisertib, and Ruxolitinib. A more comprehensive understanding of these mechanisms may open up new avenues for developing novel approaches to reducing HO in high-risk patients.

摘要

异位骨化(HO)是指一种异常过程,其特征是软组织内骨的异常发育,导致患者的活动能力和整体生活质量显著受损。巨噬细胞作为免疫系统的关键组成部分,通过其动态极化状态(促炎性M1和抗炎性M2表型)和不同细胞因子的分泌,在异位骨化的不同阶段发挥作用。本综述探讨了M1和M2巨噬细胞介导异位骨化的新机制,强调了炎症微环境、成骨因子和成骨信号通路的参与。此外,我们还探讨了针对巨噬细胞极化和功能的有前景的治疗策略,包括调节炎症微环境的药物,如白细胞介素-1抑制剂、帕罗伐他汀和二甲双胍,以及影响巨噬细胞成骨信号的药物,如转化生长因子-βRII-Fc、加鲁尼西替布和鲁索替尼。对这些机制的更全面理解可能为开发降低高危患者HO的新方法开辟新途径。

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