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微小RNA在骨重塑信号通路中的作用及其在骨质疏松症发展中的角色

The Involvement of microRNAs in Bone Remodeling Signaling Pathways and Their Role in the Development of Osteoporosis.

作者信息

Jiménez-Ortega Rogelio F, Ortega-Meléndez Alejandra I, Patiño Nelly, Rivera-Paredez Berenice, Hidalgo-Bravo Alberto, Velázquez-Cruz Rafael

机构信息

Laboratorio de Genómica del Metabolismo Óseo, Instituto Nacional de Medicina Genómica (INMEGEN), Mexico City 14610, Mexico.

Unidad de Acupuntura Humana Rehabilitatoria, Universidad Estatal del Valle de Ecatepec (UNEVE), Ecatepec de Morelos 55210, Mexico.

出版信息

Biology (Basel). 2024 Jul 7;13(7):505. doi: 10.3390/biology13070505.

Abstract

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.

摘要

骨重塑对于维持骨吸收与骨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同活动。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谱系。另一方面,在成骨细胞生成过程中,间充质干细胞(MSCs)通过TGF-β/BMP/Wnt信号通路的激活分化为成骨细胞谱系。最近的研究表明,骨重塑受包括微小RNA(miRNAs)在内的转录后机制调控。miRNAs是长度约为22个核苷酸的小单链非编码RNA。miRNAs可通过与靶mRNA的3'非翻译区(3'UTR)的miRNA反应元件(MRE)结合,几乎调控所有细胞过程。miRNAs通过在骨形成和吸收过程中调控关键信号级联反应,参与控制成骨分化过程中的基因表达。miRNA表达的改变可能有利于包括骨质疏松症在内的骨疾病的发展。本综述对参与骨重塑的miRNAs及其在骨质疏松症发展中的意义进行了概述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/539a/11273958/b5cc44c4f49c/biology-13-00505-g001.jpg

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