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骨关节炎中组蛋白翻译后修饰的图谱

Landscape of Histone Posttranslational Modifications in Osteoarthritis.

作者信息

Zhao Siyu, Zheng Jia, Yue Songkai, Chen Xiaoyang, Dong Yonghui

机构信息

Department of Orthopedics, Henan Provincial People's Hospital, People's Hospital of Zhengzhou University, Zhengzhou, Henan, People's Republic of China.

出版信息

J Inflamm Res. 2025 Jun 17;18:7893-7906. doi: 10.2147/JIR.S514599. eCollection 2025.

DOI:10.2147/JIR.S514599
PMID:40546403
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12182087/
Abstract

Osteoarthritis (OA) is a complex, progressive, and age-associated disease characterized by aberrant epigenetic expression. Epigenetic analysis has helped clarify the role of histone post-translational modifications (PTMs) in OA. PTMs affect histone structure and function and, therefore, regulate the expression of genes implicated in various biological processes. The roles of histone methylation and acetylation in OA progression-including extracellular collagen degradation and matrix destruction-have been thoroughly analyzed. Though several studies have shown that histone PTMs are related to OA, summative investigations in this area are lacking. The present literature review examines the relationships between histone PTMs and OA. It focuses mainly on methylation, acetylation, phosphorylation, lactylation, ubiquitination, and the roles of the histone methyltransferase (HMT)/histone demethylase (HDMT) and histone acetyltransferase (HAT)/histone deacetylase (HDAC) families in OA development. We used epigenetic tools for discovering new OA treatments. This review offers new perspectives for future studies on OA pathogenesis and treatment.

摘要

骨关节炎(OA)是一种复杂的、进行性的、与年龄相关的疾病,其特征在于异常的表观遗传表达。表观遗传分析有助于阐明组蛋白翻译后修饰(PTM)在OA中的作用。PTM影响组蛋白的结构和功能,因此调节参与各种生物学过程的基因的表达。组蛋白甲基化和乙酰化在OA进展中的作用,包括细胞外胶原蛋白降解和基质破坏,已经得到了深入分析。尽管有几项研究表明组蛋白PTM与OA有关,但该领域缺乏总结性研究。本文献综述探讨了组蛋白PTM与OA之间的关系。它主要关注甲基化、乙酰化、磷酸化、乳酰化、泛素化,以及组蛋白甲基转移酶(HMT)/组蛋白去甲基化酶(HDMT)和组蛋白乙酰转移酶(HAT)/组蛋白脱乙酰酶(HDAC)家族在OA发展中的作用。我们使用表观遗传工具来发现新的OA治疗方法。这篇综述为未来关于OA发病机制和治疗的研究提供了新的视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa75/12182087/c14221881c61/JIR-18-7893-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa75/12182087/7f064e3d4231/JIR-18-7893-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa75/12182087/480f9902f877/JIR-18-7893-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa75/12182087/c14221881c61/JIR-18-7893-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa75/12182087/7f064e3d4231/JIR-18-7893-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa75/12182087/480f9902f877/JIR-18-7893-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa75/12182087/c14221881c61/JIR-18-7893-g0003.jpg

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本文引用的文献

1
KLF9-GRK5-HDAC6 axis aggravates osteoarthritis pathogenesis by promoting chondrocyte extracellular matrix degradation and apoptosis.KLF9-GRK5-HDAC6轴通过促进软骨细胞外基质降解和细胞凋亡加重骨关节炎发病机制。
Commun Biol. 2025 Jan 8;8(1):23. doi: 10.1038/s42003-025-07460-x.
2
Lactate promotes microglial scar formation and facilitates locomotor function recovery by enhancing histone H4 lysine 12 lactylation after spinal cord injury.乳酸促进小胶质细胞瘢痕形成,并通过增强脊髓损伤后组蛋白 H4 赖氨酸 12 的乳酰化作用促进运动功能恢复。
J Neuroinflammation. 2024 Aug 3;21(1):193. doi: 10.1186/s12974-024-03186-5.
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Matrix stiffening promotes chondrocyte senescence and the osteoarthritis development through downregulating HDAC3.
基质僵硬通过下调 HDAC3 促进软骨细胞衰老和骨关节炎发展。
Bone Res. 2024 May 24;12(1):32. doi: 10.1038/s41413-024-00333-9.
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Regulation of cytokine and chemokine expression by histone lysine methyltransferase MLL1 in rheumatoid arthritis synovial fibroblasts.组蛋白赖氨酸甲基转移酶 MLL1 调控类风湿关节炎滑膜成纤维细胞细胞因子和趋化因子的表达。
Sci Rep. 2024 May 9;14(1):10610. doi: 10.1038/s41598-024-60860-7.
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Endothelial Cell-Derived Lactate Triggers Bone Mesenchymal Stem Cell Histone Lactylation to Attenuate Osteoporosis.内皮细胞衍生的乳酸触发骨髓间充质干细胞组蛋白乳酰化以减轻骨质疏松症。
Adv Sci (Weinh). 2023 Nov;10(31):e2301300. doi: 10.1002/advs.202301300. Epub 2023 Sep 26.
6
Inhibition of KDM7A/B histone demethylases restores H3K79 methylation and protects against osteoarthritis.抑制 KDM7A/B 组蛋白去甲基化酶可恢复 H3K79 甲基化并预防骨关节炎。
Ann Rheum Dis. 2023 Jul;82(7):963-973. doi: 10.1136/ard-2022-223789. Epub 2023 Mar 16.
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Sirt6 attenuates chondrocyte senescence and osteoarthritis progression.Sirt6 可减轻软骨细胞衰老和骨关节炎进展。
Nat Commun. 2022 Dec 10;13(1):7658. doi: 10.1038/s41467-022-35424-w.
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Novel histone post-translational modifications in diabetes and complications of diabetes: The underlying mechanisms and implications.糖尿病及并发症中新型组蛋白翻译后修饰:潜在机制与意义。
Biomed Pharmacother. 2022 Dec;156:113984. doi: 10.1016/j.biopha.2022.113984. Epub 2022 Nov 7.
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