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Tris(2-ethylhexyl) phosphate induces cytotoxicity in TM3 Leydig cells by modulating autophagy and endoplasmic reticulum stress.
Zhang, Wenqiao; Song, Yali; Yi, Letai; Ou, Jinhuan; Chen, Junhui; Zhang, Wei; Wen, Qinglian; Yang, Chuanbin; Wang, Jigang.
Afiliação
  • Zhang W; Department of Oncology, The Affiliated Hospital of Southwest Medical University, Southwest Medical University, Luzhou, Sichuan 646000, China.
  • Song Y; Dongguan Maternal and Child Health Care Hospital, Postdoctoral Innovation Practice Base of Southern Medical University, Dongguan, Guangdong 523125, China.
  • Yi L; Medicine Innovation Center for Nationalities, Inner Mongolia Medical University, Hohhot 010110, China.
  • Ou J; Department of Critical Medicine, Shenzhen Clinical Research Centre for Geriatrics, Shenzhen People's Hospital; the Second Clinical Medical College of Jinan University; the First Affiliated Hospital of Southern University of Science and Technology, Shenzhen 518020, Guangdong, China.
  • Chen J; Department of Critical Medicine, Shenzhen Clinical Research Centre for Geriatrics, Shenzhen People's Hospital; the Second Clinical Medical College of Jinan University; the First Affiliated Hospital of Southern University of Science and Technology, Shenzhen 518020, Guangdong, China.
  • Zhang W; Department of Critical Medicine, Shenzhen Clinical Research Centre for Geriatrics, Shenzhen People's Hospital; the Second Clinical Medical College of Jinan University; the First Affiliated Hospital of Southern University of Science and Technology, Shenzhen 518020, Guangdong, China.
  • Wen Q; Department of Oncology, The Affiliated Hospital of Southwest Medical University, Southwest Medical University, Luzhou, Sichuan 646000, China. Electronic address: wenqinglian@swmu.edu.cn.
  • Yang C; Department of Critical Medicine, Shenzhen Clinical Research Centre for Geriatrics, Shenzhen People's Hospital; the Second Clinical Medical College of Jinan University; the First Affiliated Hospital of Southern University of Science and Technology, Shenzhen 518020, Guangdong, China. Electronic addres
  • Wang J; Department of Oncology, The Affiliated Hospital of Southwest Medical University, Southwest Medical University, Luzhou, Sichuan 646000, China; Dongguan Maternal and Child Health Care Hospital, Postdoctoral Innovation Practice Base of Southern Medical University, Dongguan, Guangdong 523125, China; Dep
Ecotoxicol Environ Saf ; 279: 116462, 2024 Jul 01.
Article em En | MEDLINE | ID: mdl-38776784
ABSTRACT
Tris (2-ethylhexyl) phosphate (TEHP) is a frequently used organophosphorus flame retardant with significant ecotoxicity and widespread human exposure. Recent research indicates that TEHP has reproductive toxicity. However, the precise cell mechanism is not enough understood. Here, by using testicular mesenchymal stromal TM3 cells as a model, we reveal that TEHP induces apoptosis. Then RNA sequencing analysis, immunofluorescence, and western blotting results show that THEP inhibits autophagy flux and enhances endoplasmic reticulum (ER) stress. Moreover, the activation of the ER stress is critical for TEHP-induced cell injury. Interestingly, TEHP-induced ER stress is contributed to autophagic flux inhibition. Furthermore, pharmacological inhibition of autophagy aggravates, and activation of autophagy attenuates TEHP-induced apoptosis. In summary, these findings indicate that TEHP triggers apoptosis in mouse TM3 cells through ER stress activation and autophagy flux inhibition, offering a new perspective on the mechanisms underlying TEHP-induced interstitial cytotoxicity in the mouse testis.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Autofagia / Apoptose / Estresse do Retículo Endoplasmático / Retardadores de Chama / Células Intersticiais do Testículo Limite: Animals Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Autofagia / Apoptose / Estresse do Retículo Endoplasmático / Retardadores de Chama / Células Intersticiais do Testículo Limite: Animals Idioma: En Ano de publicação: 2024 Tipo de documento: Article