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相关概念视频

lncRNA - Long Non-coding RNAs02:39

lncRNA - Long Non-coding RNAs

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In humans, more than 80% of the genome gets transcribed. However, only around 2% of the genome codes for proteins. The remaining part produces non-coding RNAs which includes ribosomal RNAs, transfer RNAs, telomerase RNAs, and regulatory RNAs, among other types. A large number of regulatory non-coding RNAs have been classified into two groups depending upon their length – small non-coding RNAs, such as microRNA, which are less than 200 nucleotides in length, and long non-coding RNA...
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Treatment for a fracture is based on the type of break, the bone affected, and the patient's age.
Minor fractures with no bone displacement are treated by immobilizing the fractured bone using a cast or splint. However, in the case of fractures with displaced bones, the broken bones are repositioned before immobilization to ensure successful healing without deformation and loss of function. The realignment of fractured bone ends is performed through a process called reduction. If the...
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MicroRNA (miRNA) are short, regulatory RNA transcribed from introns (non-coding regions of a gene) or intergenic regions (stretches of DNA present between genes). Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself, forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA...
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Real-Time Imaging of CCL5-Induced Migration of Periosteal Skeletal Stem Cells in Mice
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通过miR-134-5p/XIAP轴的LncRNA LINC01123中介损伤愈合

Song Zhou1, ZeWen Zheng2, ChuanKai Zhang1

  • 1Department of Orthopedics and Joint Surgery, Xuzhou Renci Hospital, Jiangsu, Xuzhou, 221000, China.

Journal of orthopaedic surgery and research
|August 23, 2025
PubMed
概括

通过miR-134-5p/ XIAP途径抑制骨质细胞分化,提高长非编码RNALINC01123促进骨折的延迟愈合. 这表明LINC01123是骨折愈合的潜在预后标志物.

关键词:
延迟治愈时间区分方式没有.其他国家miR-134-5p的使用情况

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科学领域:

  • 分子生物学
  • 生物化学
  • 细胞生物学

背景情况:

  • 骨折愈合的延迟带来了重大的临床挑战,需要研究新的治疗点.
  • 长非编码RNAs (lncRNAs) 正在成为包括骨再生在内的生物过程的关键调节者.

研究的目的:

  • 研究 lncRNA LINC01123 在骨质细胞分化中的作用及其在延迟骨折愈合中的分子机制.
  • 探索LINC01123作为延迟骨折愈合的诊断标志物的潜力.

主要方法:

  • 实时定量聚合酶链反应 (RT-qPCR) 用于测量基因和微RNA表达水平.
  • 细胞测定包括CCK-8,流细胞测量,阿利沙林红色染色和西部斑点来评估骨质细胞功能.
  • 路西法酶活性测定以确认向相互作用和ROC曲线分析诊断潜力.

主要成果:

  • 在骨折愈合延迟的患者中,LINC01123过度表达,预测愈合延迟.
  • LINC01123上调抑制了骨质细胞分化,降低了细胞活力和增加了细胞亡.
  • 确定了miR-134-5p/ XIAP途径是LINC01123发挥作用的机制.

结论:

  • 通过miR-134-5p/ XIAP轴,增加的LINC01123表达会加剧骨折愈合的延迟.
  • LINC01123作为监测骨折愈合进展的潜在预后生物标志物.