Zhang Yu, Cao Ke-Xin, Niu Qin-Jian, Deng Jiang, Zhao Ling, Khalil Mahmoud Mohamed, Karrow Niel Alexander, Kuča Kamil, Sun Lv-Hui
State Key Laboratory of Agricultural Microbiology, Hubei Hongshan Laboratory, Frontiers Science Center for Animal Breeding and Sustainable Production, College of Animal Sciences and Technology, Huazhong Agricultural University, Wuhan, Hubei, 430070, China; Newhope Liuhe Co. Ltd., Beijing, 100102, China.
State Key Laboratory of Agricultural Microbiology, Hubei Hongshan Laboratory, Frontiers Science Center for Animal Breeding and Sustainable Production, College of Animal Sciences and Technology, Huazhong Agricultural University, Wuhan, Hubei, 430070, China.
Food Chem Toxicol. 2023 Apr;174:113682. doi: 10.1016/j.fct.2023.113682. Epub 2023 Feb 20.
The objective of this study was to identify the key glutathione S-transferase (GST) isozymes involved in the detoxification of Aflatoxin B (AFB) in ducks' primary hepatocytes. The full-length cDNA encoding the 10 GST isozymes (GST, GST3, GSTM3, MGST1, MGST2, MGST3, GSTK1, GSTT1, GSTO1 and GSTZ1) were isolated/synthesized from ducks' liver and cloned into the pcDNA3.1(+) vector. The results showed that pcDNA3.1(+)-GSTs plasmids were successfully transferred into the ducks' primary hepatocytes and the mRNA of the 10 GST isozymes were overexpressed by 1.9-3274.7 times. Compared to the control, 75 μg/L (IC) or 150 μg/L (IC) AFB treatment reduced the cell viability by 30.0-50.0% and increased the LDH activity by 19.8-58.2% in the ducks' primary hepatocytes. Notably, the AFB-induced changes in cell viability and LDH activity were mitigated by overexpression of GST and GST3. Compared to the cells treated with AFB, exo-AFB-8,9-epoxide (AFBO)-GSH, as the major detoxified product of AFB, was increased in the cells overexpression of GST and GST3. Moreover, the sequences, phylogenetic and domain analysis revealed that the GST and GST3 were orthologous to Meleagris gallopavo GSTA3 and GSTA4. In conclusion, this study found that the ducks' GST and GST3 were orthologous to Meleagris gallopavo GSTA3 and GSTA4, which were involved in the detoxification of AFB in ducks' primary hepatocytes.
本研究的目的是鉴定参与鸭原代肝细胞中黄曲霉毒素B(AFB)解毒的关键谷胱甘肽S-转移酶(GST)同工酶。从鸭肝脏中分离/合成了编码10种GST同工酶(GST、GST3、GSTM3、MGST1、MGST2、MGST3、GSTK1、GSTT1、GSTO1和GSTZ1)的全长cDNA,并将其克隆到pcDNA3.1(+)载体中。结果表明,pcDNA3.1(+)-GSTs质粒成功转入鸭原代肝细胞,10种GST同工酶的mRNA表达量上调了1.9至3274.7倍。与对照组相比,75μg/L(IC)或150μg/L(IC)的AFB处理使鸭原代肝细胞的细胞活力降低了30.0%至50.0%,并使乳酸脱氢酶(LDH)活性增加了19.8%至58.2%。值得注意的是,GST和GST3的过表达减轻了AFB诱导的细胞活力和LDH活性变化。与AFB处理的细胞相比,作为AFB主要解毒产物的外源性AFB-8,9-环氧化物(AFBO)-谷胱甘肽(GSH)在GST和GST3过表达的细胞中增加。此外,序列、系统发育和结构域分析表明,GST和GST3与家鸡的GSTA3和GSTA4是直系同源的。总之,本研究发现鸭的GST和GST3与家鸡的GSTA3和GSTA4是直系同源的,它们参与鸭原代肝细胞中AFB的解毒过程。