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DOI 10.7150/thno.55645

Медицинская библиотека · Theranostics · 2021

Deciphering the autophagy regulatory network via single-cell transcriptome analysis reveals a requirement for autophagy homeostasis in spermatogenesis.

Wang Mei, Xu Yanwen, Zhang Yuncong, Chen Yuhan, Chang Gang, An Geng, Yang Xinyan, Zheng Caihong, Zhao Jiexiang, Liu Zhaoting, Wang Dazhuang, Miao Kai, Rao Shuan, Dai Meng, Wang Dong, Zhao Xiao-Yang

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

Background

Autophagy has been implicated as a crucial component in spermatogenesis, and autophagy dysfunction can lead to reproductive disorders in animal models, including yeast, C. elegans and mice. However, the sophisticated transcriptional networks of autophagic genes throughout human spermatogenesis and their biological significance remain largely uncharacterized.

Methods

We profiled the transcriptional signatures of autophagy-related genes during human spermatogenesis by assessing specimens from nine fertile controls (including two normal persons and seven obstructive azoospermia (OA) patients) and one nonobstructive azoospermia (NOA) patient using single-cell RNA sequencing (scRNA-seq) analysis. Dysregulation of autophagy was confirmed in two additional NOA patients by immunofluorescence staining. Gene knockdown was used to identify the role of Cst3 in autophagy during spermatogenesis.

Results

Our data uncovered a unique, global stage-specific enrichment of autophagy-related genes. Human-mouse comparison analysis revealed that the stage-specific expression pattern of autophagy-related genes was highly conserved in mammals. More importantly, dysregulation of some clusters of autophagy-related genes was observed in NOA patients, suggesting the association of autophagy with male infertility. Cst3, a human-mouse conserved and autophagy-related gene that is actively expressed in spermatogonia and early spermatocytes, was found to regulate spermatogonial stem cell (SSC) maintenance and subsequent male germ cell development. Knockdown of Cst3 increased autophagic activity in mouse SSCs and subsequently suppressed the transcription of SSC core factors such as Oct4, Id1, and Nanos3, which could be efficiently rescued by manipulating autophagic activity.

Conclusions

Our study provides comprehensive insights into the global transcriptional signatures of autophagy-related genes and confirms the importance of autophagy homeostasis in SSC maintenance and normal spermatogenesis, opening new avenues for further dissecting the significance of the autophagy regulatory network in spermatogenesis as well as male infertility.

Для цитирования: Wang Mei, Xu Yanwen, Zhang Yuncong, Chen Yuhan, Chang Gang, An Geng, Yang Xinyan, Zheng Caihong, Zhao Jiexiang, Liu Zhaoting, Wang Dazhuang, Miao Kai, Rao Shuan, Dai Meng, Wang Dong, Zhao Xiao-Yang. Deciphering the autophagy regulatory network via single-cell transcriptome analysis reveals a requirement for autophagy homeostasis in spermatogenesis.. Theranostics. 2021. DOI: 10.7150/thno.55645.

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