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Aging impairs the ability of vascular endothelial stem cells to generate endothelial cells in mice.衰老会损害血管内皮干细胞在小鼠中生成内皮细胞的能力。
Angiogenesis. 2023 Nov;26(4):567-580. doi: 10.1007/s10456-023-09891-8. Epub 2023 Aug 10.
3
Enhanced Osteogenesis Potential of MG-63 Cells through Sustained Delivery of VEGF via Liposomal Hydrogel.通过脂质体水凝胶持续递送血管内皮生长因子增强MG-63细胞的成骨潜能
Gels. 2023 Jul 10;9(7):562. doi: 10.3390/gels9070562.
4
Significance of mechanical loading in bone fracture healing, bone regeneration, and vascularization.机械负荷在骨折愈合、骨再生和血管形成中的意义。
J Tissue Eng. 2023 May 22;14:20417314231172573. doi: 10.1177/20417314231172573. eCollection 2023 Jan-Dec.
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Split dCas12a activator for lncRNA H19 activation to enhance BMSC differentiation and promote calvarial bone healing.Split dCas12a 激活物激活 lncRNA H19 以增强 BMSC 分化并促进颅骨骨愈合。
Biomaterials. 2023 Jun;297:122106. doi: 10.1016/j.biomaterials.2023.122106. Epub 2023 Mar 31.
6
Exosomal Lnc NEAT1 from endothelial cells promote bone regeneration by regulating macrophage polarization via DDX3X/NLRP3 axis.内皮细胞来源的外泌体长链非编码 RNA NEAT1 通过 DDX3X/NLRP3 轴调控巨噬细胞极化促进骨再生。
J Nanobiotechnology. 2023 Mar 20;21(1):98. doi: 10.1186/s12951-023-01855-w.
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Integrated lncRNA function upon genomic and epigenomic regulation.基因组和表观基因组调控下的长链非编码 RNA 功能。
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Bevacizumab attenuates osteosarcoma angiogenesis by suppressing MIAT encapsulated by serum-derived extracellular vesicles and facilitating miR-613-mediated GPR158 inhibition.贝伐单抗通过抑制血清衍生的细胞外囊泡包裹的 MIAT 和促进 miR-613 介导的 GPR158 抑制来减弱骨肉瘤血管生成。
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长链非编码RNA在骨微环境中骨生成与血管生成相互作用中的作用

Roles of lncRNA in the crosstalk between osteogenesis and angiogenesis in the bone microenvironment.

作者信息

Zhang Shihua, Guo Jianmin, He Yuting, Su Zhi'ang, Feng Yao, Zhang Lan, Jun Zou, Weng Xiquan, Yuan Yu

机构信息

School of Exercise and Health, Guangzhou Sport University, Guangzhou 510500, China.

College of Sports and Health, Shandong Sport University, Jinan 250102, China.

出版信息

J Zhejiang Univ Sci B. 2025 Feb 25;26(2):107-123. doi: 10.1631/jzus.B2300607.

DOI:10.1631/jzus.B2300607
PMID:40015932
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11867785/
Abstract

Bone is a highly calcified and vascularized tissue. The vascular system plays a vital role in supporting bone growth and repair, such as the provision of nutrients, growth factors, and metabolic waste transfer. Moreover, the additional functions of the bone vasculature, such as the secretion of various factors and the regulation of bone-related signaling pathways, are essential for maintaining bone health. In the bone microenvironment, bone tissue cells play a critical role in regulating angiogenesis, including osteoblasts, bone marrow mesenchymal stem cells (BMSCs), and osteoclasts. Osteogenesis and bone angiogenesis are closely linked. The decrease in osteogenesis and bone angiogenesis caused by aging leads to osteoporosis. Long noncoding RNAs (lncRNAs) are involved in various physiological processes, including osteogenesis and angiogenesis. Recent studies have shown that lncRNAs could mediate the crosstalk between angiogenesis and osteogenesis. However, the mechanism by which lncRNAs regulate angiogenesis‒osteogenesis crosstalk remains unclear. In this review, we describe in detail the ways in which lncRNAs regulate the crosstalk between osteogenesis and angiogenesis to promote bone health, aiming to provide new directions for the study of the mechanism by which lncRNAs regulate bone metabolism.

摘要

骨是一种高度钙化且血管丰富的组织。血管系统在支持骨生长和修复方面起着至关重要的作用,例如提供营养物质、生长因子以及代谢废物转运。此外,骨血管系统的其他功能,如分泌各种因子和调节骨相关信号通路,对于维持骨骼健康至关重要。在骨微环境中,骨组织细胞在调节血管生成中起关键作用,包括成骨细胞、骨髓间充质干细胞(BMSCs)和破骨细胞。成骨作用和骨血管生成密切相关。衰老导致的成骨作用和骨血管生成减少会引发骨质疏松症。长链非编码RNA(lncRNAs)参与包括成骨作用和血管生成在内的各种生理过程。最近的研究表明,lncRNAs可以介导血管生成和成骨作用之间的相互作用。然而,lncRNAs调节血管生成 - 成骨作用相互作用的机制仍不清楚。在这篇综述中,我们详细描述了lncRNAs调节成骨作用和血管生成之间相互作用以促进骨骼健康的方式,旨在为研究lncRNAs调节骨代谢的机制提供新方向。