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The roles of bone‐derived exosomes and exosomal microRNAs in regulating bone remodelling

机译:骨源性外泌体和外体微RNA在调节骨重塑中的作用

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Abstract Pathological destructive bone diseases are primarily caused by the failure of a lifelong self-renewal process of the skeletal system called bone remodelling. The mechanisms underlying this process include enhanced osteoclast activity and decreased generation of the osteoblast lineage. Intercellular interaction and crosstalk among these cell types are crucial for the maintenance of bone remodelling, either through the secretion of growth factors or direct cell–cell physical engagement. Recent studies have revealed that exosomes derived from bone cells, including osteoclasts, osteoblasts and their precursors, play pivotal roles on bone remodelling by transferring biologically active molecules to target cells, especially in the processes of osteoclast and osteoblast differentiation. Here, we review the contents of bone-derived exosomes and their functions in the regulatory processes of differentiation and communication of osteoclasts and osteoblasts. In addition, we highlight the characteristics of microRNAs of bone-derived exosomes involved in the regulation of bone remodelling, as well as the potential clinical applications of bone-derived exosomes in bone remodelling disorders.
机译:摘要病理性破坏性骨病主要是由骨骼系统终生自我更新过程(称为骨骼重塑)的失败引起的。该过程的基础机制包括破骨细胞活性增强和成骨细胞谱系生成减少。这些细胞类型之间的细胞间相互作用和串扰对于维持骨骼重塑至关重要,无论是通过生长因子的分泌还是直接的细胞间物理参与。最近的研究表明,源自骨细胞的外泌体,包括破骨细胞,成骨细胞及其前体,通过将生物活性分子转移至靶细胞,尤其是在破骨细胞和成骨细胞分化过程中,对骨重塑起着关键作用。在这里,我们审查了骨源性外泌体的内容及其在破骨细胞和成骨细胞分化和传播的调控过程中的功能。此外,我们重点介绍了参与骨重塑调控的骨源性外泌体微RNA的特征,以及骨源性外泌体在骨重塑疾病中的潜在临床应用。

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