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[Effect of high selenium on insulin signaling pathway PI3K-AKT-mTOR in L02 cells].
Wang, Qin; Zhang, Xue; Wang, Jianrong; Liu, Yiqun; Han, Feng; Xiang, Xuesong; Guo, Yanbin; Huang, Zhenwu.
Affiliation
  • Wang Q; National Institute for Nutrition and Health, Chinese Center for Disease Control and Prevention, Beijing 100050, China.
  • Zhang X; National Institute for Nutrition and Health, Chinese Center for Disease Control and Prevention, Beijing 100050, China.
  • Wang J; National Institute for Nutrition and Health, Chinese Center for Disease Control and Prevention, Beijing 100050, China.
  • Liu Y; National Institute for Nutrition and Health, Chinese Center for Disease Control and Prevention, Beijing 100050, China.
  • Han F; National Institute for Nutrition and Health, Chinese Center for Disease Control and Prevention, Beijing 100050, China.
  • Xiang X; National Institute for Nutrition and Health, Chinese Center for Disease Control and Prevention, Beijing 100050, China.
  • Guo Y; College of Resources and Environmental Sciences, China Agricultural University, Beijing 100193, China.
  • Huang Z; National Institute for Nutrition and Health, Chinese Center for Disease Control and Prevention, Beijing 100050, China The Key Laboratory of Trace Element Nutrition, National Health Commission of the People's Republic of China, Beijing 100050, China.
Wei Sheng Yan Jiu ; 53(1): 77-87, 2024 Jan.
Article in Zh | MEDLINE | ID: mdl-38443176
ABSTRACT

OBJECTIVE:

To observe the effect of high selenium on insulin signaling pathway PI3K-AKT-mTOR in L02 cells.

METHODS:

One group of L02 cell was treated with different concentrations of selenomethionine(SeMet, 0.001, 0.0025, 0.005, 0.0075, 0.01, 0.025, 0.05, 0.075 and 0.1µmol/L) for 48 h, then cultured with serum-free medium for 4 h and stimulated with 1 µmol/L insulin for 15 min. The insulin signaling pathway(PI3K-AKT-mTOR) was detected by WB. Another group of L02 cell was treated with the same concentrations of SeMet as above for 48 h. The cell supernatant and lysates were collected for the analysis of SELENOP and GPX1, respectively by WB.

RESULTS:

The expressions of P-AKT-(Ser-473), P-AKT-(Thr-308), PI3K and mTOR in L02 cells under high-Se were decreased with the increase of SeMet concentration. The expressions of GPX1 and SELENOP were enhanced with the increase of SeMet.

CONCLUSION:

The insulin signaling pathway, PI3K-AKT-mTOR, was damaged in L02 cell under high-Se stress.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Selenium Language: Zh Journal: Wei Sheng Yan Jiu Journal subject: SAUDE PUBLICA Year: 2024 Document type: Article Affiliation country: China Country of publication: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Selenium Language: Zh Journal: Wei Sheng Yan Jiu Journal subject: SAUDE PUBLICA Year: 2024 Document type: Article Affiliation country: China Country of publication: China