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A noncanonical role of NOD-like receptor NLRP14 in PGCLC differentiation and spermatogenesis.
Yin, Yike; Cao, Shiyu; Fu, Huancheng; Fan, Xueying; Xiong, Jingfei; Huang, Qiuyue; Liu, Yu; Xie, Kun; Meng, Tie-Gang; Liu, Yuliang; Tang, Dan; Yang, Tingting; Dong, Biao; Qi, Shiqian; Nie, Ling; Zhang, Huiyuan; Hu, Hongbo; Xu, Wenming; Li, Fuping; Dai, Lunzhi; Sun, Qing-Yuan; Li, Zhonghan.
Afiliação
  • Yin Y; Center for Growth Metabolism & Aging, Key Laboratory of Bio-Resource and Eco-Environment of Ministry of Education, College of Life Sciences, Sichuan University, 610064 Chengdu, China.
  • Cao S; Center for Growth Metabolism & Aging, Key Laboratory of Bio-Resource and Eco-Environment of Ministry of Education, College of Life Sciences, Sichuan University, 610064 Chengdu, China.
  • Fu H; Center for Growth Metabolism & Aging, Key Laboratory of Bio-Resource and Eco-Environment of Ministry of Education, College of Life Sciences, Sichuan University, 610064 Chengdu, China.
  • Fan X; Center for Growth Metabolism & Aging, Key Laboratory of Bio-Resource and Eco-Environment of Ministry of Education, College of Life Sciences, Sichuan University, 610064 Chengdu, China.
  • Xiong J; Center for Growth Metabolism & Aging, Key Laboratory of Bio-Resource and Eco-Environment of Ministry of Education, College of Life Sciences, Sichuan University, 610064 Chengdu, China.
  • Huang Q; Center for Growth Metabolism & Aging, Key Laboratory of Bio-Resource and Eco-Environment of Ministry of Education, College of Life Sciences, Sichuan University, 610064 Chengdu, China.
  • Liu Y; Department of General Practice and National Clinical Research Center for Geriatrics, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University and Collaborative Innovation Center of Biotherapy, 610064 Chengdu, China.
  • Xie K; Center for Growth Metabolism & Aging, Key Laboratory of Bio-Resource and Eco-Environment of Ministry of Education, College of Life Sciences, Sichuan University, 610064 Chengdu, China.
  • Meng TG; State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, 100101 Beijing, China.
  • Liu Y; Fertility Preservation Lab, Reproductive Medicine Center, Guangdong Second Provincial General Hospital, 510317 Guangzhou, China.
  • Tang D; Sichuan Key Laboratory of Conservation Biology for Endangered Wildlife, Chengdu Giant Panda Breeding Research Base, 610081 Chengdu, China.
  • Yang T; Department of Urology, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University and Collaborative Innovation Center of Biotherapy, 610064 Chengdu, China.
  • Dong B; Human Sperm Bank, Key Laboratory of Birth Defects and Related Diseases of Women and Children of Ministry of Education, West China Second University Hospital of Sichuan University, 610064 Chengdu, China.
  • Qi S; Department of General Practice and National Clinical Research Center for Geriatrics, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University and Collaborative Innovation Center of Biotherapy, 610064 Chengdu, China.
  • Nie L; Department of Urology, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University and Collaborative Innovation Center of Biotherapy, 610064 Chengdu, China.
  • Zhang H; Department of Pathology, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University and Collaborative Innovation Center of Biotherapy, 610064 Chengdu, China.
  • Hu H; Department of Rheumatology and Immunology, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University and Collaborative Innovation Center of Biotherapy, 610064 Chengdu, China.
  • Xu W; Department of Rheumatology and Immunology, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University and Collaborative Innovation Center of Biotherapy, 610064 Chengdu, China.
  • Li F; Department of Obstetrics/Gynecology, Joint Laboratory of Reproductive Medicine, Key Laboratory of Obstetric, Gynecologic and Pediatric Diseases and Birth Defects of Ministry of Education, West China Second University Hospital, Sichuan University, 610064 Chengdu, China.
  • Dai L; Human Sperm Bank, Key Laboratory of Birth Defects and Related Diseases of Women and Children of Ministry of Education, West China Second University Hospital of Sichuan University, 610064 Chengdu, China.
  • Sun QY; Department of General Practice and National Clinical Research Center for Geriatrics, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University and Collaborative Innovation Center of Biotherapy, 610064 Chengdu, China.
  • Li Z; State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, 100101 Beijing, China.
Proc Natl Acad Sci U S A ; 117(36): 22237-22248, 2020 09 08.
Article em En | MEDLINE | ID: mdl-32839316
ABSTRACT
NOD-like receptors (NLRs) are traditionally recognized as major inflammasome components. The role of NLRs in germ cell differentiation and reproduction is not known. Here, we identified the gonad-specific Nlrp14 as a pivotal regulator in primordial germ cell-like cell (PGCLC) differentiation in vitro. Physiologically, knock out of Nlrp14 resulted in reproductive failure in both female and male mice. In adult male mice, Nlrp14 knockout (KO) inhibited differentiation of spermatogonial stem cells (SSCs) and meiosis, resulting in trapped SSCs in early stages, severe oligozoospermia, and sperm abnormality. Mechanistically, NLRP14 promoted spermatogenesis by recruiting a chaperone cofactor, BAG2, to bind with HSPA2 and form the NLRP14-HSPA2-BAG2 complex, which strongly inhibited ChIP-mediated HSPA2 polyubiquitination and promoted its nuclear translocation. Finally, loss of HSPA2 protection and BAG2 recruitment by NLRP14 was confirmed in a human nonsense germline variant associated with male sterility. Together, our data highlight a unique proteasome-mediated, noncanonical function of NLRP14 in PGCLC differentiation and spermatogenesis, providing mechanistic insights of gonad-specific NLRs in mammalian germline development.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Espermatogênese / Diferenciação Celular / Chaperonas Moleculares / Proteínas de Choque Térmico HSP70 / Proteínas Adaptadoras de Transdução de Sinal / Proteínas Reguladoras de Apoptose Tipo de estudo: Prognostic_studies Limite: Animals / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Espermatogênese / Diferenciação Celular / Chaperonas Moleculares / Proteínas de Choque Térmico HSP70 / Proteínas Adaptadoras de Transdução de Sinal / Proteínas Reguladoras de Apoptose Tipo de estudo: Prognostic_studies Limite: Animals / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article