Mitigating bisphenol A-induced apoptosis in KGN cells: the therapeutic role of 1,25-dihydroxyvitamin D3 through upregulation of PGC-1α expression and inhibition of the mitochondrial cytochrome c pathway.

IF 2.4 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Liting Tang, Ke Du, Kaiming Luo, Long Wang, Fei Hua
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Abstract

Purpose: This study investigated the potential of 1,25-dihydroxyvitamin D3 (1,25(OH)2VD3) to mitigate bisphenol A (BPA)-induced apoptosis in human ovarian granulosa KGN cells with the aim of establishing a theoretical foundation for understanding of how vitamin D improved ovarian function in patients with polycystic ovary syndrome (PCOS).

Methods: The impact of varying concentrations of BPA and 1,25(OH)2VD3 on KGN cell viability was elucidated. It was established that BPA-induced apoptosis in KGN cells. Subsequently, KGN cells underwent pretreatment with 1,25(OH)2VD3, followed by exposure to BPA. The apoptosis rate, reactive oxygen species (ROS) levels, and mitochondrial function of the cells were meticulously assessed, along with the expression levels of genes associated with apoptosis as well as antioxidant and mitochondrial biogenesis.

Results: BPA induced a notable increase in apoptosis (P < 0.001) and oxidative stress (P < 0.001) in KGN cells, accompanied by a significant reduction in mitochondrial membrane potential (P < 0.001) and severe impairment of mitochondrial function. Following pretreatment of KGN cells with 1,25(OH)2VD3, there was a significant decrease in the apoptosis rate (P = 0.004), coupled with a reduction in ROS production (P = 0.002). Concomitantly, the upregulation of PGC-1α (P = 0.009) and SOD (P = 0.018) was observed, while mRNA expression of BAX (P = 0.011), Cyt c (P = 0.001), Apaf-1 (P = 0.012), caspase-9 (P < 0.001), and caspase-3 (P = 0.011) was downregulated. Notably, the mitigation of mitochondrial damage was evident through restored mitochondrial membrane potential (P < 0.001), as corroborated by electron microscope results.

Conclusions: 1,25(OH)2VD3 mitigated BPA-induced damage and apoptosis in KGN cells by upregulating the expression of PGC-1α and impeding the mitochondrial cytochrome c (Cyt c) apoptotic pathway. This study established a novel theoretical foundation for utilizing vitamin D in the treatment of PCOS patients.

Abstract Image

缓解双酚 A 诱导的 KGN 细胞凋亡:1,25-二羟维生素 D3 通过上调 PGC-1α 表达和抑制线粒体细胞色素 c 途径发挥的治疗作用。
目的:本研究探讨了1,25-二羟基维生素D3(1,25(OH)2VD3)缓解双酚A(BPA)诱导的人类卵巢颗粒KGN细胞凋亡的潜力,旨在为理解维生素D如何改善多囊卵巢综合征(PCOS)患者的卵巢功能奠定理论基础:方法:阐明了不同浓度的双酚 A 和 1,25(OH)2VD3 对 KGN 细胞活力的影响。结果表明,双酚 A 可诱导 KGN 细胞凋亡。随后,对 KGN 细胞进行 1,25(OH)2VD3预处理,然后暴露于双酚 A。研究人员对细胞的凋亡率、活性氧(ROS)水平、线粒体功能以及与细胞凋亡、抗氧化和线粒体生物生成相关的基因表达水平进行了细致的评估:结果:双酚 A 诱导细胞凋亡明显增加(P 2VD3 ),但细胞凋亡率显著下降(P = 0.004),同时 ROS 产生减少(P = 0.002)。同时,还观察到 PGC-1α (P = 0.009) 和 SOD (P = 0.018) 的上调,而 BAX (P = 0.011)、Cyt c (P = 0.001)、Apaf-1 (P = 0.012)、caspase-9(P 结论:1,25(OH)2VD3 对细胞凋亡有抑制作用:1,25(OH)2VD3通过上调PGC-1α的表达和阻碍线粒体细胞色素c(Cyt c)凋亡途径,减轻了双酚A诱导的KGN细胞损伤和凋亡。这项研究为利用维生素D治疗多囊卵巢综合症患者奠定了新的理论基础。
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来源期刊
CiteScore
5.90
自引率
0.00%
发文量
76
审稿时长
6-12 weeks
期刊介绍: Hormones-International Journal of Endocrinology and Metabolism is an international journal published quarterly with an international editorial board aiming at providing a forum covering all fields of endocrinology and metabolic disorders such as disruption of glucose homeostasis (diabetes mellitus), impaired homeostasis of plasma lipids (dyslipidemia), the disorder of bone metabolism (osteoporosis), disturbances of endocrine function and reproductive capacity of women and men. Hormones-International Journal of Endocrinology and Metabolism particularly encourages clinical, translational and basic science submissions in the areas of endocrine cancers, nutrition, obesity and metabolic disorders, quality of life of endocrine diseases, epidemiology of endocrine and metabolic disorders.
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