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[Triptolide induces autophagy of ovarian granulosa cells via PI3K/AKT/m TOR pathway]
Jun Bai1, Ye-Ke Wu2, Ke-Ming Wu2
1Affiliated Hospital of Shaanxi University of Chinese Medicine Xianyang 712000,China.
Abstract:
The aim of this paper was to observe the concentration,time and mechanism of autophagy induced by triptolide( TP) in ovarian granulosa cells( OGCs). CCK-8 method was used to compare the inhibitory effects of TP at different concentrations on primary cultured rat OGCs and IC50 was calculated. The effects of TP at different concentrations and time points on the expression of OGCs autophagy factor protein and the cascade of PI3 K/AKT/m TOR pathway were detected by Western blot. The effects of TP,autophagy inducer( brefeldin A) and PI3 K/m TOR inhibitor( NVP-BEZ235) on the expression of PI3 K/AKT/m TOR cascade and autophagy related factor protein were detected by Western blot. The results show that the IC50 of different concentrations of TP on OGCs of rat ovary was14. 65 μmol·L-1,and the minimum inhibitory concentration of TP was 0. 1 μmol·L-1( 100 nmol·L-1). Compared with the control group,the expression levels of beclin1 and LC3Ⅱ in each group were significantly higher than those in the control group( P<0. 05 or P<0. 01). After 12 hours of treatment with TP,brefeldin A and NVP-BEZ235,respectively,compared with the control group,TP could significantly promote the expression level of downstream autophagy effect or molecule beclin1,LC3Ⅱ and inhibit the expression level of LC3Ⅰ,p62 protein( P<0. 05 or P< 0. 01). Moreover,the expression of beclin1 and LC3Ⅱ/LC3Ⅰ in TP group was higher than that in brefeldin A group( P<0. 05 or P<0. 01),and the expression of p62 in TP group was lower than that in brefeldin A group( P<0. 05 or P<0. 01). At the same time,TP could significantly inhibit the expression of p-PI3 K,p-AKT,p-mTOR protein,and the inhibitory effect of TP was better than that of NVP-BEZ235 group. This study suggests that 100 nmol·L-1 TP could induce OGCs autophagy successfully in cultured rat ovary for 12 h; TP may induce OGCs autophagy by inhibiting PI3 k/Akt/m TOR signaling pathway.
Insights
Triptolide (TP) effectively induces autophagy in ovarian granulosa cells (OGCs) at a concentration of 100 nmol·L-1 for 12 hours. This process is mediated by inhibiting the PI3K/Akt/mTOR signaling pathway, offering insights into TP
Area of Science:
- Cell Biology
- Molecular Biology
- Reproductive Biology
Background:
- Ovarian granulosa cells (OGCs) play a crucial role in ovarian function.
- Autophagy is a vital cellular process implicated in various physiological and pathological conditions.
- Triptolide (TP) is a compound with known biological activities, but its effect on OGC autophagy requires elucidation.
Purpose of the Study:
- To investigate the concentration, time, and mechanism of autophagy induction by triptolide (TP) in ovarian granulosa cells (OGCs).
- To determine the effective concentration and duration for TP-induced autophagy in OGCs.
- To elucidate the molecular pathway involved in TP-mediated autophagy in OGCs.
Main Methods:
- Cell viability was assessed using the CCK-8 assay to determine the IC50 of TP on primary cultured rat OGCs.
- Western blot analysis was employed to detect the expression levels of autophagy-related proteins (beclin1, LC3) and the PI3K/Akt/mTOR signaling pathway components.
- Comparative analysis was performed using TP, an autophagy inducer (brefeldin A), and a PI3K/mTOR inhibitor (NVP-BEZ235).
Main Results:
- The IC50 of TP on rat OGCs was determined to be 14.65 μmol·L-1, with a minimum inhibitory concentration of 0.1 μmol·L-1 (100 nmol·L-1).
- TP treatment significantly upregulated the expression of autophagy markers beclin1 and LC3-II while downregulating LC3-I and p62.
- TP inhibited the phosphorylation of PI3K, Akt, and mTOR, suggesting a mechanism involving the suppression of the PI3K/Akt/mTOR pathway.
Conclusions:
- Triptolide (TP) at 100 nmol·L-1 effectively induces autophagy in cultured rat ovarian granulosa cells (OGCs) within 12 hours.
- TP-induced autophagy in OGCs appears to be mediated through the inhibition of the PI3K/Akt/mTOR signaling pathway.
- These findings provide novel insights into the cellular mechanisms of TP action in ovarian cells.
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