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毒死蜱通过影响 TCRγ 依赖性 PI3K/AKT/JNK 通路诱导鲤鱼淋巴细胞凋亡和自噬。

Chlorpyrifos induces apoptosis and autophagy in common carp lymphocytes by influencing the TCR γ-dependent PI3K/AKT/JNK pathway.

机构信息

College of Veterinary Medicine, Northeast Agricultural University, Harbin, 150030, PR China.

College of Veterinary Medicine, Northeast Agricultural University, Harbin, 150030, PR China; Key Laboratory of the Provincial Education, Department of Heilongjiang for Common Animal Disease Prevention and Treatment, College of Veterinary Medicine, Northeast Agricultural University, Harbin, 150030, PR China.

出版信息

Fish Shellfish Immunol. 2020 Apr;99:587-593. doi: 10.1016/j.fsi.2020.02.039. Epub 2020 Feb 26.

Abstract

Chlorpyrifos is an insecticide that is widely used in agricultural production. However, little is known about how chlorpyrifos disrupts lymphocyte homeostasis in common carp. Herein, we identified TCRγ through the results of transcriptome analysis. Subsequently, we established TCR γ knockdown and overexpression models in carp head kidney lymphocyte respectively using RNA interference and the pcDNA3.1 plasmid, respectively. Real-time PCR, fluorescent staining, ultrastructure observation and flow cytometry were used to detect the levels of the PI3K/AKT pathway, autophagy and apoptosis. Our results demonstrated that chlorpyrifos significantly decreased the expression of TCR γ, TCR γ suppression thereby induced increased mRNA expression of TNF-α, Bax, caspase-3, caspase-8, caspase-9 and significantly inhibited the expression of Bcl-2, which indicated that apoptosis was triggered. This conclusion was supported by our flow cytometry and ultrastructure observation results. In addition, the control and TCR γ overexpression groups had normal cell morphology. Moreover, TCR γ suppression activated the expression of Becline-1, ATG5, ATG10, ATG12, ATG16 and reduced the expression of mTOR, with the opposite results observed in the TCR γ overexpression group. Together, these results suggested that TCR γ imbalance triggers apoptosis and autophagy in lymphocyte. Moreover, we found that TCR γ knockdown significantly increased the mRNA expression of JNK and decreased the expression of PI3K and AKT, which indicated that the PI3K/AKT/JNK pathway was activated. Our results reported here indicated that chlorpyrifos induces apoptosis and autophagy in head kidney lymphocyte through the inhibition of TCR γ.

摘要

毒死蜱是一种广泛应用于农业生产的杀虫剂。然而,关于毒死蜱如何破坏鲤鱼淋巴细胞的体内平衡知之甚少。在此,我们通过转录组分析的结果鉴定了 TCRγ。随后,我们分别使用 RNA 干扰和 pcDNA3.1 质粒在鲤鱼头肾淋巴细胞中建立了 TCRγ 敲低和过表达模型。实时 PCR、荧光染色、超微结构观察和流式细胞术用于检测 PI3K/AKT 通路、自噬和细胞凋亡的水平。我们的结果表明,毒死蜱显著降低了 TCRγ的表达,TCRγ抑制导致 TNF-α、Bax、caspase-3、caspase-8 和 caspase-9 的 mRNA 表达显著增加,并显著抑制了 Bcl-2 的表达,这表明触发了细胞凋亡。这一结论得到了我们的流式细胞术和超微结构观察结果的支持。此外,对照组和 TCRγ过表达组的细胞形态正常。此外,TCRγ抑制激活了 Becline-1、ATG5、ATG10、ATG12、ATG16 的表达,降低了 mTOR 的表达,而在 TCRγ过表达组中则观察到相反的结果。综上所述,这些结果表明 TCRγ失衡会触发淋巴细胞中的细胞凋亡和自噬。此外,我们发现 TCRγ 敲低显著增加了 JNK 的 mRNA 表达并降低了 PI3K 和 AKT 的表达,这表明 PI3K/AKT/JNK 通路被激活。我们在这里报告的结果表明,毒死蜱通过抑制 TCRγ诱导头肾淋巴细胞发生细胞凋亡和自噬。

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