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软骨下骨破骨细胞功能中的非编码 RNA 及其在骨关节炎治疗中的潜在作用。

Noncoding RNAs in subchondral bone osteoclast function and their therapeutic potential for osteoarthritis.

机构信息

Department of Orthopaedics, Shenzhen Intelligent Orthopaedics and Biomedical Innovation Platform, Guangdong Artificial Intelligence Biomedical Innovation Platform, Shenzhen Second People's Hospital, The First Affiliated Hospital of Shenzhen University Health Science Center, Shenzhen, 518035, China.

Department of Child and Adolescent Psychiatry, Shenzhen Kangning Hospital, Shenzhen Mental Health Center, Shenzhen Key Laboratory for Psychological Healthcare & Shenzhen Institute of Mental Health, Shenzhen, 518003, China.

出版信息

Arthritis Res Ther. 2020 Nov 25;22(1):279. doi: 10.1186/s13075-020-02374-x.

Abstract

Osteoclasts are the only cells that perform bone resorption. Noncoding RNAs (ncRNAs) are crucial epigenetic regulators of osteoclast biological behaviors ranging from osteoclast differentiation to bone resorption. The main ncRNAs, including miRNAs, circRNAs, and lncRNAs, compose an intricate network that influences gene transcription processes related to osteoclast biological activity. Accumulating evidence suggests that abnormal osteoclast activity leads to the disturbance of subchondral bone remodeling, thus initiating osteoarthritis (OA), a prevalent joint disease characterized mainly by cartilage degradation and subchondral bone remodeling imbalance. In this review, we delineate three types of ncRNAs and discuss their related complex molecular signaling pathways associated with osteoclast function during bone resorption. We specifically focused on the involvement of noncoding RNAs in subchondral bone remodeling, which participate in the degradation of the osteochondral unit during OA progression. We also discussed exosomes as ncRNA carriers during the bone remodeling process. A better understanding of the roles of ncRNAs in osteoclast biological behaviors will contribute to the treatment of bone resorption-related skeletal diseases such as OA.

摘要

破骨细胞是唯一具有骨吸收功能的细胞。非编码 RNA(ncRNA)是破骨细胞生物学行为(从破骨细胞分化到骨吸收)的关键表观遗传调控因子。主要的 ncRNA,包括 miRNA、circRNA 和 lncRNA,构成了一个复杂的网络,影响与破骨细胞生物学活性相关的基因转录过程。越来越多的证据表明,异常的破骨细胞活性导致软骨下骨重塑紊乱,从而引发骨关节炎(OA),这是一种常见的关节疾病,主要特征是软骨降解和软骨下骨重塑失衡。在这篇综述中,我们描述了三种类型的 ncRNA,并讨论了它们与破骨细胞功能相关的复杂分子信号通路,这些通路与骨吸收过程中的破骨细胞功能有关。我们特别关注了非编码 RNA 在软骨下骨重塑中的参与,它参与了 OA 进展过程中骨软骨单位的降解。我们还讨论了外泌体作为骨重塑过程中 ncRNA 的载体。更好地了解 ncRNA 在破骨细胞生物学行为中的作用将有助于治疗与骨吸收相关的骨骼疾病,如 OA。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d44/7690185/377bf17b86ae/13075_2020_2374_Fig1_HTML.jpg

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