微小 RNA 在骨重塑信号通路中的参与及其在骨质疏松症发展中的作用

Biology Pub Date : 2024-07-07 DOI:10.3390/biology13070505
Rogelio F. Jiménez-Ortega, A. I. Ortega-Meléndez, N. Patiño, B. Rivera-Paredez, A. Hidalgo-Bravo, R. Velázquez-Cruz
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引用次数: 0

摘要

骨重塑对维持骨吸收和形成之间的平衡至关重要,它依赖于破骨细胞和成骨细胞的协调活动。在破骨细胞生成过程中,造血干细胞(HSCs)通过 OPG/RANK/RANKL 信号通路分化为破骨细胞系。另一方面,在成骨细胞生成过程中,间充质干细胞(MSCs)通过激活信号通路 TGF-β/BMP/Wnt 向成骨细胞系分化。最近的研究表明,骨重塑受转录后机制(包括微小核糖核酸(miRNA))的调控。miRNA 是长度约为 22 个核苷酸的小型单链非编码 RNA。miRNA 通过与目标 mRNA 的 3' 非翻译区(3′UTR)的 miRNA 响应元件(MRE)结合,可调控几乎所有的细胞过程。miRNA 通过调控骨形成和吸收过程中的关键信号级联,参与控制成骨分化过程中的基因表达。miRNA 表达的改变可能会导致骨质疏松症等骨科疾病的发生。本综述概述了参与骨重塑的 miRNA 及其在骨质疏松症发展中的意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Involvement of microRNAs in Bone Remodeling Signaling Pathways and Their Role in the Development of Osteoporosis
Bone remodeling, crucial for maintaining the balance between bone resorption and formation, relies on the coordinated activity of osteoclasts and osteoblasts. During osteoclastogenesis, hematopoietic stem cells (HSCs) differentiate into the osteoclast lineage through the signaling pathways OPG/RANK/RANKL. On the other hand, during osteoblastogenesis, mesenchymal stem cells (MSCs) differentiate into the osteoblast lineage through activation of the signaling pathways TGF-β/BMP/Wnt. Recent studies have shown that bone remodeling is regulated by post-transcriptional mechanisms including microRNAs (miRNAs). miRNAs are small, single-stranded, noncoding RNAs approximately 22 nucleotides in length. miRNAs can regulate virtually all cellular processes through binding to miRNA-response elements (MRE) at the 3’ untranslated region (3′UTR) of the target mRNA. miRNAs are involved in controlling gene expression during osteogenic differentiation through the regulation of key signaling cascades during bone formation and resorption. Alterations of miRNA expression could favor the development of bone disorders, including osteoporosis. This review provides a general description of the miRNAs involved in bone remodeling and their significance in osteoporosis development.
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