Lim Seung Joon, Shin Sangsu, Lee Sang In
Department of Animal Science and Biotechnology, Kyungpook National University, Sangju-si 37224, Republic of Korea.
Research Institute for Innovative Animal Science, Department of Animal Science and Biotechnology, Kyungpook National University, Sangju-si 37224, Republic of Korea.
Toxics. 2025 Apr 18;13(4):315. doi: 10.3390/toxics13040315.
Citrinin (CTN) is a mycotoxin that adversely affects livestock by contaminating stored grains, leading to significant health and economic impacts. This study investigates the toxicological effects of CTN on porcine small intestinal epithelial cells (IPEC-J2) and explores potential mitigation strategies using natural products and chemical inhibitors. Our study demonstrates that CTN induces cytotoxicity through the TGF-β signaling pathway, triggering apoptosis and G2/M phase cell cycle arrest. We examined cell viability, cell cycle progression, and gene expression changes in IPEC-J2 cells treated with CTN, 4'-Hydroxydehydrokawain (4-HDK), and LY-364947, a TGF-β receptor inhibitor. LY-364947 treatment confirmed that CTN-induced toxicity is mediated through TGF-β signaling. Although 4-HDK alleviated CTN-induced cytotoxicity by improving cell viability and reducing apoptosis, its direct involvement in TGF-β inhibition remains unclear. These results suggest that CTN disrupts intestinal epithelial cell homeostasis via TGF-β activation, whereas 4-HDK may exert protective effects through an alternative mechanism. Our study provides novel insights into CTN-induced toxicity mechanisms and highlights the therapeutic potential of 4-HDK as a mitigator of mycotoxin-induced cellular damage.
桔霉素(CTN)是一种霉菌毒素,通过污染储存的谷物对家畜产生不利影响,从而导致重大的健康和经济影响。本研究调查了CTN对猪小肠上皮细胞(IPEC-J2)的毒理学效应,并探索使用天然产物和化学抑制剂的潜在缓解策略。我们的研究表明,CTN通过TGF-β信号通路诱导细胞毒性,引发细胞凋亡和G2/M期细胞周期阻滞。我们检测了用CTN、4'-羟基脱氢卡瓦因(4-HDK)和TGF-β受体抑制剂LY-364947处理的IPEC-J2细胞的细胞活力、细胞周期进程和基因表达变化。LY-364947处理证实CTN诱导的毒性是通过TGF-β信号介导的。虽然4-HDK通过提高细胞活力和减少细胞凋亡减轻了CTN诱导的细胞毒性,但其是否直接参与抑制TGF-β仍不清楚。这些结果表明,CTN通过激活TGF-β破坏肠道上皮细胞稳态,而4-HDK可能通过另一种机制发挥保护作用。我们的研究为CTN诱导的毒性机制提供了新的见解,并突出了4-HDK作为霉菌毒素诱导细胞损伤缓解剂的治疗潜力。