97%,内毒素<0.1EU/μg,高纯度高活性低内毒素批间一致,属CX3C趋化因子家族,可趋化中性粒细胞与T淋巴细胞,参与炎症反应调控、免疫细胞招募,适用于免疫机制研究、炎症疾病药物开发、细胞迁移实验、神经生物学探究。" data-qmeta="description">

永利3044(中国集团)有限公司官网

分子生物学
IVD分子诊断
细胞培养与分析
蛋白研究
细胞因子
重组蛋白
抗体
高通量测序建库
病原检测UCF系列
生物医药
工具酶
抑制剂激活剂与常用试剂
仪器
耗材

The thioredoxin expression of Cristaria plicata is regulated by Nrf2/ARE pathway under microcystin stimulation

Maolin Feng, Yingping Gui, Jinhua An, XinYing Cao, Wuting Lu, Gang Yang, Shaoqing Jian, Baoqing Hu, Chungen Wen

Journal:INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES

IF:8.2

DOI:10.1016/j.ijbiomac.2023.124509

PMID:37085063

Published:2023-04-19

research field:分子生物学毒理学环境科学

Abstract

Thioredoxin plays an important role in inhibiting apoptosis and protecting cells from oxidative stress. This study was aimed to clarify how the expression of Trx from Cristaria plicata is regulated by Nrf2/ARE pathway. The expression of Cp Trx mRNA was significantly up-regulated in gill and kidney tissues under microcystin stress. The Nrf2 gene of Cristaria plicata was identified to possess an auto active domain bit. While Cp Nrf2 was knocked down by specific small RNA, Cp Trx mRNA expression was significantly down-regulated. The promoter of Cp Trx gene had high transcriptional activity, and this basic transcriptional activity persisted after ARE element mutation. The region of promoter −206 to +217 bp was a core promoter region and had forward regulatory elements. Gel shift Assay exhibited that the Cp Trx promoter could bind to the purified proteins Cp Nrf2 and Cp MafK in vitro. The binding phenomenon disappeared after the ARE element mutation in promoter region. Subcellular localization experiments displayed that fluorescence overlap between Cp Nrf2 and Trx promoter increased under microcystin toxin stress. These results suggested that Trx expression was regulated by Nrf2/ARE pathway under oxidative stress.

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