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本文引用的文献

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Type H vessels-a bridge connecting subchondral bone remodelling and articular cartilage degeneration in osteoarthritis development.H型血管——骨关节炎发展过程中连接软骨下骨重塑与关节软骨退变的桥梁。
Rheumatology (Oxford). 2023 Apr 3;62(4):1436-1444. doi: 10.1093/rheumatology/keac539.
2
Controlled mechanical loading improves bone regeneration by regulating type H vessels in a S1Pr1-dependent manner.控制性机械负荷通过以S1Pr1依赖性方式调节H型血管来改善骨再生。
FASEB J. 2022 Oct;36(10):e22530. doi: 10.1096/fj.202200339RRR.
3
Macrophage miR-149-5p induction is a key driver and therapeutic target for BRONJ.巨噬细胞 miR-149-5p 的诱导是 BRONJ 的关键驱动因素和治疗靶点。
JCI Insight. 2022 Aug 22;7(16):e159865. doi: 10.1172/jci.insight.159865.
4
Non-coding RNA delivery for bone tissue engineering: Progress, challenges, and potential solutions.用于骨组织工程的非编码RNA递送:进展、挑战及潜在解决方案
iScience. 2022 Jul 20;25(8):104807. doi: 10.1016/j.isci.2022.104807. eCollection 2022 Aug 19.
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TGFβ1-modified MSC-derived exosome attenuates osteoarthritis by inhibiting PDGF-BB secretion and H-type vessel activity in the subchondral bone.TGFβ1 修饰的 MSC 来源的外泌体通过抑制软骨下骨中 PDGF-BB 的分泌和 H 型血管活性来减轻骨关节炎。
Acta Histochem. 2022 Oct;124(7):151933. doi: 10.1016/j.acthis.2022.151933. Epub 2022 Aug 4.
6
miR-188-3p targets skeletal endothelium coupling of angiogenesis and osteogenesis during ageing.miR-188-3p 靶向衰老过程中血管生成和骨生成的骨骼内皮细胞耦联。
Cell Death Dis. 2022 May 25;13(5):494. doi: 10.1038/s41419-022-04902-w.
7
Long non-coding RNA HCAR promotes endochondral bone repair by upregulating VEGF and MMP13 in hypertrophic chondrocyte through sponging miR-15b-5p.长链非编码RNA HCAR通过海绵化miR-15b-5p上调肥大软骨细胞中的VEGF和MMP13来促进软骨内骨修复。
Genes Dis. 2020 Aug 10;9(2):456-465. doi: 10.1016/j.gendis.2020.07.013. eCollection 2022 Mar.
8
A bone-targeted engineered exosome platform delivering siRNA to treat osteoporosis.一种用于递送小干扰RNA以治疗骨质疏松症的骨靶向工程外泌体平台。
Bioact Mater. 2021 Sep 17;10:207-221. doi: 10.1016/j.bioactmat.2021.09.015. eCollection 2022 Apr.
9
Osteoblast-derived EGFL6 couples angiogenesis to osteogenesis during bone repair.成骨细胞衍生的 EGFL6 在骨修复过程中将血管生成与成骨偶联。
Theranostics. 2021 Sep 27;11(20):9738-9751. doi: 10.7150/thno.60902. eCollection 2021.
10
ncRNAs in Therapeutics: Challenges and Limitations in Nucleic Acid-Based Drug Delivery.ncRNAs 在治疗中的应用:基于核酸的药物递送的挑战和局限性。
Int J Mol Sci. 2021 Oct 27;22(21):11596. doi: 10.3390/ijms222111596.

[非编码RNA对骨H型血管生成的调控]

[Regulation of non-coding RNA in type H vessels angiogenesis of bone].

作者信息

Tang Shengping, Liao Shijie, Liu Jianhong, Luo Xiaolin, Wei Zhendi, Ding Xiaofei

机构信息

Department of Trauma Orthopedic and Hand Surgery, the First Affiliated Hospital of Guangxi Medical University, Nanning Guangxi, 530021, P. R. China.

出版信息

Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2023 Aug 15;37(8):1042-1048. doi: 10.7507/1002-1892.202304032.

DOI:10.7507/1002-1892.202304032
PMID:37586808
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10435345/
Abstract

OBJECTIVE

To summarize the regulatory effect of non-coding RNA (ncRNA) on type H vessels angiogenesis of bone.

METHODS

Recent domestic and foreign related literature about the regulation of ncRNA in type H vessels angiogenesis was widely reviewed and summarized.

RESULTS

Type H vessels is a special subtype of bone vessels with the ability to couple bone formation. At present, the research on ncRNA regulating type H vessels angiogenesis in bone diseases mainly focuses on microRNA, long ncRNA, and small interfering RNA, which can affect the expressions of hypoxia inducible factor 1α, platelet derived growth factor BB, slit guidance ligand 3, and other factors through their own unique ways of action, thus regulating type H vessels angiogenesis and participating in the occurrence and development of bone diseases.

CONCLUSION

At present, the mechanism of ncRNA regulating bone type H vessels angiogenesis has been preliminarily explored. With the deepening of research, ncRNA is expected to be a new target for the diagnosis and treatment of vascular related bone diseases.

摘要

目的

总结非编码RNA(ncRNA)对骨H型血管生成的调控作用。

方法

广泛查阅并总结近期国内外有关ncRNA对H型血管生成调控的相关文献。

结果

H型血管是骨血管的一种特殊亚型,具有耦联骨形成的能力。目前,关于ncRNA在骨疾病中调控H型血管生成的研究主要集中于微小RNA、长链ncRNA和小干扰RNA,它们可通过自身独特的作用方式影响缺氧诱导因子1α、血小板衍生生长因子BB、缝隙引导配体3等因子的表达,从而调控H型血管生成并参与骨疾病的发生发展。

结论

目前,ncRNA调控骨H型血管生成的机制已得到初步探索。随着研究的深入,ncRNA有望成为血管相关性骨疾病诊断和治疗的新靶点。