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巨噬细胞:软骨再生的潜在靶点

Macrophage: A Potential Target on Cartilage Regeneration.

机构信息

Sports Medicine Division, Institute of Orthopedics and Traumatology, Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.

Hospital Sírio-Libanês, São Paulo, Brazil.

出版信息

Front Immunol. 2020 Feb 11;11:111. doi: 10.3389/fimmu.2020.00111. eCollection 2020.

Abstract

Cartilage lesions and osteoarthritis (OA) presents an ever-increasing clinical and socioeconomic burden. Synovial inflammation and articular inflammatory environment are the key factor for chondrocytes apoptosis and hypertrophy, ectopic bone formation and OA progression. To effectively treat OA, it is critical to develop a drug that skews inflammation toward a pro-chondrogenic microenvironment. In this narrative and critical review, we aim to see the potential use of immune cells modulation or cell therapy as therapeutic alternatives to OA patients. Macrophages are immune cells that are present in synovial lining, with different roles depending on their subtypes. These cells can polarize to pro-inflammatory (M1) and anti-inflammatory (M2) phenotypes, being the latter associated with wound-healing by the production of ARG-1 and pro-chondrogenic cytokines, such as IL-10, IL-1RA, and TGF-b. Emerging evidence reveals that macrophage shift can be determined by several stimuli, apart from the conventional IL-4, IL-13, and IL-10. Evidences show the potential of physical exercise to induce type 2 response, favoring M2 polarization. Moreover, macrophages in contact with oxLDL have effect on the production of anabolic mediators as TGF-b. In the same direction, type II collagen, that plays a critical role in development and maturation process of chondrocytes, can also induce M2 macrophages, increasing TGF-b. The mTOR pathway activation in macrophages was shown to be able to polarize macrophages , though further studies are required. The possibility to use mesenchymal stem cells (MSCs) in cartilage restoration have a more concrete literature, besides, MSCs also have the capability to induce M2 macrophages. In the other direction, M1 polarized macrophages inhibit the proliferation and viability of MSCs and impair their ability to immunosuppress the environment, preventing cartilage repair. Therefore, even though MSCs therapeutic researches advances, other sources of M2 polarization are attractive issues, and further studies will contribute to the possibility to manipulate this polarization and to use it as a therapeutic approach in OA patients.

摘要

软骨损伤和骨关节炎(OA)给临床和社会经济带来了日益增长的负担。滑膜炎症和关节炎症环境是软骨细胞凋亡和肥大、异位骨形成和 OA 进展的关键因素。为了有效治疗 OA,开发一种能使炎症向促软骨生成微环境倾斜的药物至关重要。在这篇叙述性和批判性综述中,我们旨在探讨免疫细胞调节或细胞治疗作为 OA 患者治疗选择的潜在用途。巨噬细胞是存在于滑膜衬里中的免疫细胞,根据其亚型有不同的作用。这些细胞可以极化为促炎(M1)和抗炎(M2)表型,后者通过产生 ARG-1 和促软骨生成细胞因子,如 IL-10、IL-1RA 和 TGF-b,与伤口愈合有关。新出现的证据表明,除了传统的 IL-4、IL-13 和 IL-10 之外,巨噬细胞的转变可以由多种刺激因素决定。有证据表明,体育锻炼有潜力诱导 2 型反应,有利于 M2 极化。此外,与 oxLDL 接触的巨噬细胞对合成代谢介质如 TGF-b 的产生有影响。在同一方向上,在软骨细胞的发育和成熟过程中起关键作用的 II 型胶原也可以诱导 M2 巨噬细胞,增加 TGF-b。已经表明,巨噬细胞中 mTOR 途径的激活能够使巨噬细胞极化,尽管还需要进一步的研究。间充质干细胞(MSCs)在软骨修复中的应用有更具体的文献,此外,MSCs 还具有诱导 M2 巨噬细胞的能力。另一方面,M1 极化的巨噬细胞抑制 MSCs 的增殖和活力,并损害其抑制环境免疫抑制的能力,从而阻止软骨修复。因此,尽管 MSCs 的治疗研究取得了进展,但其他 M2 极化来源是一个有吸引力的问题,进一步的研究将有助于操纵这种极化,并将其作为 OA 患者的一种治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69af/7026000/2a74dee7ea80/fimmu-11-00111-g0001.jpg

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