摘要
该研究分离并鉴定了原代小鼠子宫内膜基质细胞(mouse endometrial stromal cell,m ESC)。过表达类固醇生成因子-1(steroidogenic factor-1,SF-1)可显著诱导该细胞的增殖能力、促进增殖相关基因PCNA(proliferating cell nuclear antigen)及PH3(phospho-histone 3)的蛋白质水平表达增高以及激活PI3K-AKT-m TOR信号通路;PI3K信号通路抑制剂LY294002和m TOR信号通路抑制剂Rapamycin等可抑制mESC中SF-1过表达所引起p AKT S473、pm TOR S2448、pp70S6K T389、p S6 S235/236和p4E-BP1 T37/46的蛋白质水平的增高。该研究初步揭示了SF-1表达与mESC增殖的相关性。
Mouse endometrial stromal cell (mESC) was isolated and identified in this study. Forced expression of steroidogenic factor-1 (SF-1) in mESC induced proliferation increase and upregulation of protein expression in proliferation marker genes PH3 (phospho-histone 3) and PCNA (proliferating cell nuclear antigen) and acitivation of PI3K-AKT-mTOR signaling pathway. The PI3K signaling pathway inhibitor LY294002 and roTOR signal pathway inhibitor Rapamycin decreased the expression of pAKT S473, pmTOR $2448, pp70S6K T389, pS6 S235/236 and p4E-BP1 T37/46, which were induced by forced expression of SF-1 in primary cultured mESC. Our study provided preliminary evidences that SF-1 expression might associated with mESC cell proliferation.
出处
《中国细胞生物学学报》
CAS
CSCD
2016年第11期1317-1324,共8页
Chinese Journal of Cell Biology
基金
国家自然科学基金(批准号:31571190
81671493)
重庆市教委科技项目(批准号:渝教人(2014)47号
KJ130309)资助的课题~~