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暴露于高温会影响小鼠睾丸中与PIWI相互作用的RNA及相关转录本的表达。

Exposure to elevated temperature affects the expression of PIWI-interacting RNAs and associated transcripts in mouse testes.

作者信息

Chen Wenbin, Zhao Zhang, Cen Shengren, Lv Daojun, Wu Jun, Zhou Xumin, Yang Taowei, Zhao Tianxin, Hou Longlong, Mao Xiangming

机构信息

Department of Urology, Zhujiang Hospital, Southern Medical University, Guangzhou, Guangdong, China.

Department of Urology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, Guangdong, China.

出版信息

Andrology. 2023 May;11(4):724-737. doi: 10.1111/andr.13381. Epub 2023 Jan 29.

Abstract

BACKGROUND

Exposure to heat waves could result in adverse effects on human health, especially in male testicles. PIWI-interacting RNA (piRNA) is a novel type of small non-coding RNA, which can notably impact mRNA turnover and preserve germline maintenance in germline cells. However, piRNA's expression status when adapting to testicular heat stress remains largely unclear.

OBJECTIVES

To investigate the function and mechanisms of relevant piRNAs during testicular heat stress.

MATERIALS AND METHODS

In this study, a mouse testicular heat stress model was constructed, and the testes were removed for piRNA-sequencing. Bioinformatics analysis was used to discover the differential expressed piRNAs, piRNA clusters, and enriched pathways. A cell heat stress model was constructed to validate the top five upregulated piRNAs. Proliferation and apoptosis assays were utilized to validate the function of selected piRNA. Bioinformatics prediction, western blotting, and immunohistochemistry were used to illustrate the downstream mechanisms.

RESULTS

Through the bioinformatics analysis, we identified the differential expression profile and enriched pathways of piRNAs and piRNA clusters during testicular hyperthermia. Besides, piR-020492 was proved to be upregulated in heat stress mouse testes and a germ cell model. A series of in vitro assays illustrated that an overexpression of piR-020492 could restrain the proliferation and promote the apoptosis of mouse germ cells. Kyoto Encyclopedia of Genes and Genomes analysis of piRNA-generating genes in the testicular heat stress model and piR-020492 targeting genes showed that the overlap pathways are adenosine monophosphate-activated protein kinase (AMPK) and insulin pathways. Validation experiments demonstrated that the key genes of AMPK and insulin pathway exhibit differential expression after an overexpression of piR-020492 or testicular heat stress.

DISCUSSION AND CONCLUSION

In conclusion, our findings revealed the expression profile of piRNAs in testicular heat stress and illustrated the function and mechanisms of piR-020492 in germ cells, which could provide novel insights into the mechanism of hyperthermia-induced testicular injury.

摘要

背景

暴露于热浪中可能会对人体健康产生不利影响,尤其是对男性睾丸。PIWI相互作用RNA(piRNA)是一种新型的小非编码RNA,它可以显著影响mRNA周转并维持生殖细胞系中的生殖系维持。然而,piRNA在适应睾丸热应激时的表达状态仍不清楚。

目的

研究睾丸热应激期间相关piRNA的功能和机制。

材料与方法

在本研究中,构建了小鼠睾丸热应激模型,并取出睾丸进行piRNA测序。利用生物信息学分析来发现差异表达的piRNA、piRNA簇和富集途径。构建细胞热应激模型以验证上调程度最高的5种piRNA。利用增殖和凋亡检测来验证所选piRNA的功能。采用生物信息学预测、蛋白质免疫印迹和免疫组织化学来阐明下游机制。

结果

通过生物信息学分析,我们确定了睾丸高温期间piRNA和piRNA簇的差异表达谱及富集途径。此外,piR-020492在热应激小鼠睾丸和生殖细胞模型中被证明上调。一系列体外实验表明,piR-020492的过表达可抑制小鼠生殖细胞的增殖并促进其凋亡。对睾丸热应激模型中产生piRNA的基因和piR-020492靶向基因进行京都基因与基因组百科全书分析表明,重叠途径为腺苷单磷酸激活蛋白激酶(AMPK)和胰岛素途径。验证实验表明,piR-020492过表达或睾丸热应激后,AMPK和胰岛素途径的关键基因表现出差异表达。

讨论与结论

总之,我们的研究结果揭示了睾丸热应激中piRNA的表达谱,并阐明了piR-020492在生殖细胞中的功能和机制,这可为热疗诱导睾丸损伤的机制提供新的见解。

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