The Antioxidant Role of Selenium via GPx1 and GPx4 in LPS-Induced Oxidative Stress in Bovine Endometrial Cells
Autor: | Xiaoyu Li, Rui Feng, S.O. Adeniran, Guixue Zhang, Olamigoke O Ifarajimi, Ziming Wang, Elikanah Olusayo Adegoke, Mingjun Ma, Peng Zheng, Fushuo Huang |
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Rok vydání: | 2021 |
Předmět: |
GPX1
Antioxidant Lipopolysaccharide Endocrinology Diabetes and Metabolism medicine.medical_treatment Clinical Biochemistry 010501 environmental sciences GPX4 medicine.disease_cause 01 natural sciences Biochemistry Inorganic Chemistry 03 medical and health sciences chemistry.chemical_compound Western blot medicine 0105 earth and related environmental sciences chemistry.chemical_classification 0303 health sciences medicine.diagnostic_test Chemistry Glutathione peroxidase 030302 biochemistry & molecular biology Biochemistry (medical) General Medicine Molecular biology Enzyme Oxidative stress |
Zdroj: | Biological Trace Element Research. 200:1140-1155 |
ISSN: | 1559-0720 0163-4984 |
DOI: | 10.1007/s12011-021-02731-0 |
Popis: | This study investigated the antioxidant role of selenium (Se) in the form of selenomethionine (SLM) in LPS-induced oxidative stress via the glutathione peroxidase (GPx) enzymes and the Nrf2/HO-1 transcription factor. The impact of serum supplementation in culture media on GPxs was also studied. The bovine uterus is constantly exposed to exogenous pathogens postpartum, and the endometrium is the first contact against bacteria invasion. Endometritis is an inflammation of the endometrium and is brought about by bacterial lipopolysaccharide capable of inducing oxidative stress. The BEND cells were supplemented at the point of seeding with the following SLM concentrations 0, 100, 500, and 1000 nM for 48 h. BEND cells, cultured with or without SLM (100 nM), were initially incubated for 48 h, and then, we serum starved the SLM group for 24, 48, and 72 h. Similarly, an assay involving serum volume (0, 2, 5, and 10%) supplementation in culture media (v/v) with or without SLM (100 nM) was performed for 48 h. The BEND cells were also seeded into four experimental groups and cultured for an initial 48 h as follows: control, LPS (20 μg/mL), SLM (100 nM), and SLM + LPS groups followed by 6-h LPS treatment. The role of SLM in modulating the expressions of GPx1 and GPx4 and the Nrf2 transcription factor-related genes was assessed using qRT-PCR and Western blot techniques. The results showed serum starvation in the presence of SLM supplementation decreased the expression of GPx1 enzyme but increased GPx4 compared to the control. The addition of SLM to cell culture media in an FBS limiting condition improved the expressions of both GPx1 and GPx4. SLM supplementation promoted GPx enzymes' expressions in a serum-free media (0%) and at 2% FBS in media. However, it did not improve their expressions at 10% FBS in media than the untreated groups. Together, our data show the protective role of Se by regulating the expressions of GPx1 and GPx4 enzymes in BEND cells. It also shows that SLM promoted the expression of Nrf2 transcription factor-related genes at both the mRNA and protein levels in BEND cells during LPS stimulation. |
Databáze: | OpenAIRE |
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