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尿外泌体tRNA衍生小RNA的表达谱及其在草酸钙结石病中的潜在作用。

Expression profiles of urine exosomal tRNA-derived small RNAs and their potential roles in calcium oxalate stone disease.

作者信息

Hong Sen-Yuan, Miao Lin-Tao, Yang Yuan-Yuan, Wang Shao-Gang

机构信息

Department of Urology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

出版信息

Ann Med Surg (Lond). 2024 Sep 10;86(10):5802-5810. doi: 10.1097/MS9.0000000000002563. eCollection 2024 Oct.

Abstract

BACKGROUND AND OBJECTIVE

Exosomes have been confirmed to be implicated in the pathogenesis of calcium oxalate (CaOx) stones. tRNA-derived small RNAs (tsRNAs) are among the oldest small RNAs involved in exosome-mediated intercellular communication, yet their role in kidney stones remains unexplored. This pilot study aimed to identify differentially expressed tsRNAs (DEtsRNAs) in urine exosomes between CaOx stone patients and healthy controls and explore their potential roles in nephrolithiasis.

METHOD

First-morning urine samples were collected from three CaOx stone patients and three healthy controls. Urinary exosomes were isolated and analyzed by high-throughput sequencing to generate the expression profiles of tsRNAs and detect DEtsRNAs. Predicted target genes of DEtsRNAs were subjected to functional enrichment analysis. The authors also combined the public dataset GSE73680 to investigate how DEtsRNAs were related to stone formation.

RESULTS

Four DEtsRNAs were significantly upregulated in CaOx stone patients compared to healthy controls. tRF-Lys-TTT-5005c was the most elevated, followed by tRF-Lys-CTT-5006c, tRF-Ala-AGC-5017b, and tRF-Gly-CCC-5004b. Bioinformatics analysis indicated that these four types of DEtsRNAs might serve distinct biological functions. Combined with data mining from the public dataset GSE73680, the authors assumed that exosomes carrying tRF-Lys-TTT-5005c and tRF-Lys-CTT-5006c could inhibit the expression of SMAD6, FBN1, and FZD1, thereby activating the BMP signaling pathway, which might induce an osteogenic-like transformation in target cells, resulting in the formation of Randall's plaques and CaOx stones.

CONCLUSION

The authors' findings shed light on the potential roles of tsRNAs in the pathogenesis of CaOx stone disease, highlighting exosomal DEtsRNAs as promising diagnostic biomarkers and therapeutic targets in nephrolithiasis.

摘要

背景与目的

外泌体已被证实与草酸钙(CaOx)结石的发病机制有关。tRNA衍生的小RNA(tsRNAs)是参与外泌体介导的细胞间通讯的最古老的小RNA之一,但其在肾结石中的作用仍未被探索。这项初步研究旨在鉴定CaOx结石患者与健康对照者尿液外泌体中差异表达的tsRNAs(DEtsRNAs),并探讨它们在肾结石病中的潜在作用。

方法

收集3例CaOx结石患者和3例健康对照者的首次晨尿样本。分离尿液外泌体并通过高通量测序进行分析,以生成tsRNAs的表达谱并检测DEtsRNAs。对DEtsRNAs的预测靶基因进行功能富集分析。作者还结合公共数据集GSE73680来研究DEtsRNAs与结石形成的关系。

结果

与健康对照相比,CaOx结石患者中有4种DEtsRNAs显著上调。tRF-Lys-TTT-5005c升高最为明显,其次是tRF-Lys-CTT-5006c、tRF-Ala-AGC-5017b和tRF-Gly-CCC-5004b。生物信息学分析表明,这四种类型的DEtsRNAs可能具有不同的生物学功能。结合来自公共数据集GSE73680的数据挖掘,作者推测携带tRF-Lys-TTT-5005c和tRF-Lys-CTT-5006c的外泌体可能抑制SMAD6、FBN1和FZD-1的表达,从而激活BMP信号通路,这可能诱导靶细胞发生成骨样转化,导致兰德尔斑和CaOx结石的形成。

结论

作者的研究结果揭示了tsRNAs在CaOx结石病发病机制中的潜在作用,突出了外泌体DEtsRNAs作为肾结石病有前景的诊断生物标志物和治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef47/11444539/713e6eac0468/ms9-86-5802-g001.jpg

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