Melatonin attenuates palmitic acid-induced mouse granulosa cells apoptosis via endoplasmic reticulum stress

被引:63
作者
Chen, Zhi [1 ]
Lei, Lanjie [2 ,3 ]
Wen, Di [1 ]
Yang, Lei [3 ,4 ]
机构
[1] Qiannan Normal Univ Nationlities, Coll Biol Sci & Agr, Duyun 5580009, Guizhou, Peoples R China
[2] Jiujiang Univ, Affiliated Hosp, Jiujiang 332000, Jiangxi, Peoples R China
[3] Jiujiang Univ, Key Lab Syst Biomed Jiangxi Prov, Jiujiang 332000, Jiangxi, Peoples R China
[4] Jiujiang Univ, Coll Basic Med Sci, Jiujiang 332000, Jiangxi, Peoples R China
关键词
Palmitic acid; Melatonin; Endoplasmic reticulum stress; Mouse granulosa cell; Apoptosis; IN-VITRO MATURATION; FATTY-ACIDS; OXIDATIVE STRESS; FOLLICULAR-FLUID; BOVINE-OOCYTES; DAIRY-COWS; ATRESIA; KNOCKDOWN; FOLLICLES; PROTECTS;
D O I
10.1186/s13048-019-0519-z
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
BackgroundPalmitic acid (PA), the main component of dietary saturated fat, causes apoptosis in many cell types, including mouse granulosa cell. Melatonin, an important endogenous hormone, has beneficial effects on female reproductive processes. Since elevated PA levels are present in follicular fluid (FF) of patients with infertility and are shown to be toxic for granulosa cells, we investigated the molecular mechanisms of PA toxicity in mouse granulosa cells and explored the effects of melatonin on PA-induced apoptosis.MethodsGranulosa cells from immature female mice were cultured for 24h in medium containing PA and/or melatonin. Then, the effects of PA alone or combined with melatonin on viability, apoptosis and endoplasmic reticulum (ER) stress in granulosa cells were detected by methyl thiazolyl tetrazolium (MTT) assay, flow cytometry assay and western blot. After 48h of PA and/or melatonin treatment, the concentrations of estradiol (E2) and progesterone (P4) in the culture supernatants were measured with ELISA kits.ResultsIn this study, we explored the effects of melatonin on cell viability and apoptosis in PA-treated mouse granulosa cells and uncovered the signaling pathways involved in these processes. Our results showed that 200-800M PA treatment reduces cell viability, induces cell apoptosis, enhances the expression of apoptosis-related genes (Caspase 3 and B-cell lymphoma-2 (BCL-2) associated X protein (BAX)), and activates the expression of ER stress marker genes (glucose-regulated protein 78 (GRP78) and CCAAT/enhancer binding protein homologous protein (CHOP)). Melatonin treatment (1-10M) suppresses 400M PA-induced cell viability decrease, cell apoptosis, Caspase 3 activation, and BAX, CHOP, and GRP78 expression. In addition, we found that 10M melatonin successfully attenuated the 400M PA-induced estrogen (E2) and progesterone (P4) decreases.ConclusionsThis study suggests that PA triggers cell apoptosis via ER stress and that melatonin protects cells against apoptosis by inhibiting ER stress in mouse granulosa cells.
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页数:12
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