Shi Haixia, Yan Zunqiang, Du Hong, Gun Shuangbao
College of Animal Science and Technology, Gansu Agricultural University, Lanzhou 730030, China.
Gansu Innovation Research Center for Swine Production Engineering and Technology, Lanzhou 730070, China.
Antioxidants (Basel). 2025 Apr 5;14(4):439. doi: 10.3390/antiox14040439.
Zearalenone (ZEA) is a widespread mycotoxin that contaminates cereals and other animal feeds. Sertoli cells (SCs) are the main target of attack by many environmental toxins. Our previous study found that L. polysaccharides (PAP-1b) exhibited protective effects against ZEA-induced oxidative damage in testicular SCs. However, the regulatory mechanisms remain incompletely characterized. In this study, SCs were treated with a complete medium (CON group) or medium containing 150 μg/mL PAP-1b (PAP-1b group). After 4 h, 100 μM ZEA was added to the ZEA group and PAP-1b-ZEA group, respectively. Samples were collected after the cells continued to be incubated for 48 h and subsequently subjected to transcriptome sequencing. The results showed that 1018, 7183, and 1023 differentially expressed genes (DEGs) were screened in the CON-vs.-PAP-1b, CON-vs.-ZEA, and ZEA-vs.-PAP-1b-ZEA groups, respectively. Among them, glutathione peroxidase 1 () emerges as a key gene within this antioxidant defense mechanism. In addition, these DEGs were significantly enriched in Gene Ontology (GO) terms related to oxidative stress as well as in MAPK and PI3K-AKT signaling pathways, suggesting that PAP-1b effectively mitigated ZEA-induced oxidative damage in SCs by regulating these signaling pathways. These results provide an essential basis for the further elucidation of the role of PAP-1b in mitigating ZEA-induced oxidative damage in SCs.
玉米赤霉烯酮(ZEA)是一种广泛存在的霉菌毒素,可污染谷物和其他动物饲料。支持细胞(SCs)是许多环境毒素的主要攻击目标。我们之前的研究发现,L.多糖(PAP-1b)对ZEA诱导的睾丸支持细胞氧化损伤具有保护作用。然而,其调控机制仍不完全清楚。在本研究中,支持细胞分别用完全培养基(CON组)或含150μg/mL PAP-1b的培养基(PAP-1b组)处理。4小时后,分别向ZEA组和PAP-1b-ZEA组加入100μM ZEA。细胞继续孵育48小时后收集样本,随后进行转录组测序。结果显示,在CON与PAP-1b、CON与ZEA、ZEA与PAP-1b-ZEA组中分别筛选出1018、7183和1023个差异表达基因(DEGs)。其中,谷胱甘肽过氧化物酶1()在这种抗氧化防御机制中成为关键基因。此外,这些DEGs在与氧化应激相关的基因本体(GO)术语以及MAPK和PI3K-AKT信号通路中显著富集,表明PAP-1b通过调节这些信号通路有效减轻了ZEA诱导的支持细胞氧化损伤。这些结果为进一步阐明PAP-1b在减轻ZEA诱导的支持细胞氧化损伤中的作用提供了重要依据。