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胰岛素样生长因子2信使核糖核酸结合蛋白2通过过氧化物酶体增殖物激活受体γ/细胞原癌基因FOS调控的双途径:活化T细胞核因子1信号传导和自噬相关16样蛋白2介导的自噬驱动颞下颌关节骨关节炎的软骨下骨损伤

Insulin-Like Growth Factor 2 mRNA-Binding Protein 2 Drives Subchondral Bone Damage in Temporomandibular Joint Osteoarthritis through Peroxisome Proliferator-Activated Receptor γ/Cellular FOS Proto-oncogene-Regulated Dual Pathways: Nuclear Factor of Activated T Cells 1 Signaling and Autophagy-Related 16-Like 2-Mediated Autophagy.

作者信息

Jiang Ziyan, Zhao Jie, Liang Youde, Gao Zhao, Sun Yanan, Hu Yaying, Pan Junchen, Long Xing, Zhang Jiali

机构信息

State Key Laboratory of Oral and Maxillofacial Reconstruction and Regeneration, Key Laboratory of Oral Biomedicine Ministry of Education, Hubei Key Laboratory of Stomatology, School and Hospital of Stomatology, Wuhan University, Wuhan, China; Department of Oral Pathology, School of Stomatology, Wuhan University, Wuhan, China.

State Key Laboratory of Oral and Maxillofacial Reconstruction and Regeneration, Key Laboratory of Oral Biomedicine Ministry of Education, Hubei Key Laboratory of Stomatology, School and Hospital of Stomatology, Wuhan University, Wuhan, China.

出版信息

Am J Pathol. 2025 Aug;195(8):1484-1503. doi: 10.1016/j.ajpath.2025.04.008. Epub 2025 Apr 30.

Abstract

Overactivated osteoclastogenesis leading to abnormal subchondral bone loss is the main feature of temporomandibular joint osteoarthritis (TMJOA) deterioration. The role of N6-methyladenosine in osteoclast-mediated subchondral bone loss in TMJOA remains unknown. Here, it was found that an N6-methyladenosine reader insulin-like growth factor 2 mRNA-binding protein 2 (IGF2BP2) was essential for mature osteoclast induction. In TMJ tissues of patients with TMJOA, the expression of IGF2BP2 was increased. Moreover, IGF2BP2 was augmented in subchondral bone of monosodium iodoacetate (MIA)-induced TMJOA mice. Igf2bp2 deficiency attenuated MIA-induced subchondral bone loss and suppressed osteoclast function. Mechanistically, IGF2BP2 directly stabilized Pparg and Fos mRNA to enhance the nuclear factor of activated T cells 1 (NFATC1) signaling, thereby inducing osteoclast maturation. Furthermore, the stabilized peroxisome proliferator-activated receptor γ (PPARγ) promoted the transcription of Fos, resulting in a further amplified signaling of NFATC1. In Igf2bp2-deficient cells, overexpression of PPARγ and cellular FOS proto-oncogene (C-FOS) rescued the function of osteoclasts through restoring reduced levels of NFATC1. On the other hand, the IGF2BP2/PPARγ/C-FOS axis facilitated the formation of osteoclasts by restoring the inhibited autophagy levels through the down-regulation of autophagy-related 16-like 2. IGF2BP2 inhibitor, CWI1-2, hindered osteoclast formation and mitigated synovial inflammation, cartilage degeneration, and bone destruction in MIA-induced TMJOA mice. In summary, IGF2BP2 may be a novel regulator of osteoclastogenesis of TMJOA pathogenesis, which aggravates TMJOA pathology via stabilizing Pparg and Fos mRNA, thereby promoting NFATC1-mediated osteoclast signaling and autophagy-related 16-like 2-mediated autophagy.

摘要

破骨细胞生成过度激活导致下颌关节骨关节炎(TMJOA)恶化的主要特征是异常的软骨下骨丢失。N6-甲基腺苷在TMJOA中破骨细胞介导的软骨下骨丢失中的作用仍然未知。在这里,发现一种N6-甲基腺苷阅读器胰岛素样生长因子2 mRNA结合蛋白2(IGF2BP2)对成熟破骨细胞的诱导至关重要。在TMJOA患者的颞下颌关节组织中,IGF2BP2的表达增加。此外,在碘乙酸钠(MIA)诱导的TMJOA小鼠的软骨下骨中IGF2BP2增加。Igf2bp2缺乏减弱了MIA诱导的软骨下骨丢失并抑制了破骨细胞功能。机制上,IGF2BP2直接稳定Pparg和Fos mRNA以增强活化T细胞1(NFATC1)信号通路的核因子,从而诱导破骨细胞成熟。此外,稳定的过氧化物酶体增殖物激活受体γ(PPARγ)促进Fos的转录,导致NFATC1信号通路进一步放大。在Igf2bp2缺陷细胞中,PPARγ和细胞FOS原癌基因(C-FOS)的过表达通过恢复降低的NFATC1水平挽救了破骨细胞的功能。另一方面,IGF2BP2/PPARγ/C-FOS轴通过下调自噬相关16样蛋白2来恢复受抑制的自噬水平,从而促进破骨细胞的形成。IGF2BP2抑制剂CWI1-2阻碍了破骨细胞的形成,并减轻了MIA诱导的TMJOA小鼠的滑膜炎、软骨退变和骨破坏。总之,IGF2BP2可能是TMJOA发病机制中破骨细胞生成的一种新型调节因子,它通过稳定Pparg和Fos mRNA来加重TMJOA病理,从而促进NFATC1介导的破骨细胞信号通路和自噬相关16样蛋白2介导的自噬。

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