Decoding the spermatogonial stem cell niche under physiological and recovery conditions in adult mice and humans

Author:

Jin Cheng123ORCID,Wang Zhipeng1ORCID,Li Pengyu1,Tang Jielin1,Jiao Tao1,Li Yiran1,Ou Jinhuan1,Zou Dingfeng1,Li Mengzhen1,Mang Xinyu1,Liu Jun1,Ma Yanni14,Wu Xiaolong5,Shi Jie5,Chen Shitao6,He Manman1,Lu Yan1,Zhang Ning47ORCID,Miao Shiying1,Sun Fei5,Wang Linfang1,Li Kai1ORCID,Yu Jia14ORCID,Song Wei1ORCID

Affiliation:

1. Department of Biochemistry and Molecular Biology, State Key Laboratory of Common Mechanism Research for Major Diseases, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, School of Basic Medicine, Peking Union Medical College, Beijing 100005, China.

2. Affiliated Foshan Maternity and Child Healthcare Hospital, Southern Medical University (Foshan Maternity & Child Healthcare Hospital), Foshan 528000, China.

3. Department of Developmental Biology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, Guangdong, China.

4. Center for Stem Cell and Regeneration Medicine, Chinese Academy of Medical Sciences & Peking Union Medical College (PUMC), Chengdu 610052, China.

5. Institute of Reproductive Medicine, School of Medicine, Nantong University, Nantong 226001, China.

6. International Peace Maternity and Child Health Hospital, Shanghai Key Laboratory for Reproductive Medicine, School of Medicine, Shanghai Jiaotong University, Shanghai 200030, China.

7. Medical Research Council Protein Phosphorylation and Ubiquitylation Unit (MRC-PPU), School of Life Sciences, University of Dundee, Dundee DD1 5EH, UK.

Abstract

The intricate interaction between spermatogonial stem cell (SSC) and testicular niche is essential for maintaining SSC homeostasis; however, this interaction remains largely uncharacterized. In this study, to characterize the underlying signaling pathways and related paracrine factors, we delineated the intercellular interactions between SSC and niche cell in both adult mice and humans under physiological conditions and dissected the niche-derived regulation of SSC maintenance under recovery conditions, thus uncovering the essential role of C-C motif chemokine ligand 24 and insulin-like growth factor binding protein 7 in SSC maintenance. We also established the clinical relevance of specific paracrine factors in human fertility. Collectively, our work on decoding the adult SSC niche serves as a valuable reference for future studies on the aetiology, diagnosis, and treatment of male infertility.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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