Melatonin Alleviates Oxidative Stress Induced by H₂O₂ in Porcine Trophectoderm Cells

• Main Authors: Yawei Fu (Author), Yue Chen (Author), Zhao Jin (Author), Hu Gao (Author), Gang Song (Author), Qian Wang (Author), Kang Xu (Author)
• Format: Book
• Published: MDPI AG, 2022-05-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.
• Notes: 10.3390/antiox11061047; 2076-3921
• Keywords: Placental; PTr2 cells; ROS; cell viability; apoptosis; Therapeutics. Pharmacology; RM1-950
• Source: Antioxidants, Vol 11, Iss 6, p 1047 (2022)

Placental oxidative stress has been implicated as a main risk factor for placental dysfunction. Alleviation of oxidative stress and enhancement of antioxidant capacity of porcine trophectoderm (PTr2) cells are effective means to maintaining normal placental function. The present study was conducted to evaluate the protective effect of melatonin (MT) on H₂O₂-induced oxidative damage in PTr2 cells. Our data revealed that pretreatment with MT could significantly improve the decrease in cell viability induced by H₂O₂, and reduce intracellular reactive oxygen species (ROS) levels and the ratio of apoptotic cells. Here, we compared the transcriptomes of untreated versus melatonin-treated PTr2 cells by RNA-seq analysis and found that differentially expressed genes (DEGs) were highly enriched in the Wnt signaling, TGF-beta signaling and mTOR signaling pathways. Moreover, pretreatment with MT upregulated the antioxidant-related genes such as early growth response3 (EGR3), WAP four-disulfide core domain1 (WFDC1), heme oxygenase1 (HMOX1) and vimentin (VIM). These findings reveal that melatonin protects PTr2 cells from H₂O₂-induced oxidative stress damage.