Melatonin Protects Mouse Type A Spermatogonial Stem Cells against Oxidative Stress via The Mitochondrial Thioredoxin System

被引:0
作者
Heidarizadi, Somayeh [1 ]
Rashidi, Zahra [1 ,2 ]
Jalili, Cyrus [1 ,3 ]
Mansouri, Kamran [3 ]
Rashidi, Iraj [1 ]
Mahaki, Behzad [4 ]
Gholami, Mohammadreza [5 ,6 ]
机构
[1] Kermanshah Univ Med Sci, Fac Med, Kermanshah, Iran
[2] Kermanshah Univ Med Sci, Hlth Technol Inst, Fertil & Infertil Res Ctr, Kermanshah, Iran
[3] Kermanshah Univ Med Sci, Hlth Technol Inst, Med Biol Res Ctr, Kermanshah, Iran
[4] Kermanshah Univ Med Sci, Sch Hlth, Dept Biostat, Kermanshah, Iran
[5] Kermanshah Univ Med Sci, Inst Hlth Technol, Med Technol Res Ctr, Kermanshah, Iran
[6] Kermanshah Univ Med Sci, Inst Hlth Technol, Med Technol Res Ctr, POB 6714869914, Kermanshah, Iran
关键词
Melatonin; Oxidative Stress; Spermatogonia; REDUCTIVE CARBOXYLATION; REDOX HOMEOSTASIS; EXPRESSION; TOXICITY; INVOLVEMENT; METABOLISM; GLUCOSE; TISSUE;
D O I
10.22074/CELLJ.2023.2003766.1316
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Objective: Mitochondrial oxidative stress is an important factor in infertility. The mitochondrial thioredoxin system plays an important role in this condition. N-acetyl-5-methoxy tryptamine (melatonin) plays a role in reducing oxidative stress and apoptosis in spermatogonial stem cells (SSCs). In this study, we explore the probable protective effects of melatonin on the mitochondrial thioredoxin system [thioredoxin 2 (Trx2)/Txnip] in SSCs under oxidative stress. Materials and Methods: In this experimental study, SSCs were co-cultured two-dimensionally (2D) with Sertoli cells in DMEM culture medium that contained 10% fetal bovine serum (FBS), 1% antibiotics, and 10 ng/ml glial cell-derived neurotrophic factor (GDNF) for 30 days. The cultured cells were subsequently divided into four groups: control; melatonin (250 pM, 24 hours); melatonin (250 pM, 24 hours)+hydrogen peroxide (H2O2, 50 pM, 24 hours); and H2O2 (50 pM, 24 hours). Intracellular reactive oxygen species (ROS) production was determined by flow cytometry. Malondialdehyde (MDA) levels were measured by Fluorometry. The expressions of apoptotic and antioxidant genes and nuclear factor erythroid 2-related factor 2 (Nrf2), Trx2, and nicotinamide nucleotide transhydrogenase (NNT) proteins were determined by quantitative real-time polymerase chain reaction (qRT-PCR) and Western blot. Adenosine triphosphate (ATP) levels were measured by fluorometry. Results: Melatonin reduced H2O2-induced ROS levels and apoptosis in the SSCs. Melatonin also increased mRNA expression of Nrf2, Trx2, NNT, Sirtuin 3 (Sirt3), and decreased mRNA expression of Txnip, and increased protein expressions of Nrf2, Trx2, NNT thereby increasing activity of the mitochondrial thioredoxin system. In addition, melatonin Conclusion: Melatonin increased Trx2 expression through the Nrf2 pathway. This study suggests that melatonin may protect SSCs from oxidative stress in diseases related to infertility.
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收藏
页码:741 / 752
页数:12
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