Chaveroux Cédric, Carraro Valérie, Canaple Laurence, Averous Julien, Maurin Anne-Catherine, Jousse Céline, Muranishi Yuki, Parry Laurent, Mesclon Florent, Gatti Evelina, Mallet Jacques, Ravassard Philippe, Pierre Philippe, Fafournoux Pierre, Bruhat Alain
Institut National de la Recherche Agronomique (INRA), UMR 1019 Nutrition Humaine, Centre de Clermont-Ferrand-Theix, 63122 Saint Genès Champanelle, France. Université Clermont 1, UFR Médecine, UMR 1019 Nutrition Humaine, 63000 Clermont-Ferrand, France.
Institut de Génomique Fonctionnelle de Lyon, IGFL UMR 5242 CNRS, ENS Lyon, INRA 1288, UCBL, 69364 Lyon, France.
Sci Signal. 2015 Apr 28;8(374):rs5. doi: 10.1126/scisignal.aaa0549.
The eIF2α-ATF4 pathway is involved in cellular adaptation to stress and is dysregulated in numerous diseases. Activation of this pathway leads to phosphorylation of the α subunit of eukaryotic initiation factor 2 (eIF2α) and the recruitment of the transcription factor ATF4 (activating transcription factor 4) to specific CCAAT/enhancer binding protein (C/EBP)-ATF response elements (CAREs) located in the promoters of target genes. To monitor the spatiotemporal modulation of this pathway in living animals, we generated a novel CARE-driven luciferase mouse model (CARE-LUC). These transgenic mice enable the investigation of the eIF2α-ATF4 pathway activity in the whole organism and at the tissue and cellular levels by combining imaging, luciferase assays, and immunochemistry. Using this mouse line, we showed the tissue-specific activation pattern of this pathway in response to amino acid deficiency or endoplasmic reticulum stress and the hepatic induction of this pathway in a stress-related pathology model of liver fibrosis. The CARE-LUC mouse model represents an innovative tool to investigate the eIF2α-ATF4 axis and to develop drugs targeting this important pathway in the remediation of related pathologies.
真核起始因子2α-激活转录因子4(eIF2α-ATF4)信号通路参与细胞对压力的适应过程,且在多种疾病中失调。该信号通路的激活会导致真核起始因子2(eIF2α)的α亚基磷酸化,并促使转录因子ATF4(激活转录因子4)募集至位于靶基因启动子区域的特定CCAAT/增强子结合蛋白(C/EBP)-ATF反应元件(CAREs)上。为监测活体动物中该信号通路的时空调节情况,我们构建了一种新型的CARE驱动的荧光素酶小鼠模型(CARE-LUC)。这些转基因小鼠通过结合成像、荧光素酶检测和免疫化学技术,能够在整体动物、组织及细胞水平上研究eIF2α-ATF4信号通路的活性。利用该小鼠品系,我们展示了该信号通路在应对氨基酸缺乏或内质网应激时的组织特异性激活模式,以及在肝纤维化应激相关病理模型中该信号通路在肝脏中的诱导情况。CARE-LUC小鼠模型是一种创新工具,可用于研究eIF2α-ATF4轴,并开发针对这一重要信号通路的药物,以修复相关病理状况。