Boussabbeh Manel, Ben Salem Intidhar, Prola Alexandre, Guilbert Arnaud, Bacha Hassen, Abid-Essefi Salwa, Lemaire Christophe
*Laboratory for Research on Biologically Compatible Compounds, Faculty of Dentistry, Rue Avicenne, 5019 Monastir, Tunisia, INSERM UMR-S 1180, LabEx LERMIT, Faculty of Pharmacy, Université Paris-Sud, Faculté de Pharmacie, 92296 Châtenay-Malabry, France and Université de Versailles Saint Quentin en Yvelines, 78035 Versailles, France.
*Laboratory for Research on Biologically Compatible Compounds, Faculty of Dentistry, Rue Avicenne, 5019 Monastir, Tunisia, INSERM UMR-S 1180, LabEx LERMIT, Faculty of Pharmacy, Université Paris-Sud, Faculté de Pharmacie, 92296 Châtenay-Malabry, France and Université de Versailles Saint Quentin en Yvelines, 78035 Versailles, France
Toxicol Sci. 2015 Apr;144(2):328-37. doi: 10.1093/toxsci/kfu319. Epub 2015 Jan 9.
Patulin (PAT) is a toxic metabolite produced by several filamentous fungi of the genera of Penicillium, Aspergillus, and Byssochlamys. PAT is the most common mycotoxin found in apples and apple-based products including juice, compotes, cider, and baby food. Exposure to this mycotoxin has been reported to induce intestinal and kidney injuries. This study investigated the mechanism of PAT-induced toxicity in human colon carcinoma (HCT116) and embryonic kidney cells (HEK293). We demonstrated that PAT activated endoplasmic reticulum (ER) and unfolded protein response as evidenced by up-regulation of GRP78 and GADD34, splicing of XBP1 mRNA, and expression of the proapoptotic factor CHOP. This ER stress response was accompanied by the induction of the mitochondrial apoptotic pathway. Apoptosis occurred with ROS production, drop in mitochondrial membrane potential and caspase activation. Further, we showed that deficiency of the proapoptotic protein Bax or Bak protected cells against PAT-induced apoptosis. The treatment of cells with the ROS scavenger N-acetyl cysteine inhibits the ER stress response and prevents mitochondrial apoptosis. Collectively, our data provide new mechanistic insights in the signaling pathways of the cell death induced by PAT and demonstrate that PAT induces cytotoxicity through a ROS-dependent mechanism involving ER stress and activation of mitochondrial apoptotic pathway in human intestinal and kidney cells.
展青霉素(PAT)是由青霉属、曲霉属和丝衣霉属的几种丝状真菌产生的一种有毒代谢产物。PAT是在苹果及苹果制品(包括果汁、果脯、苹果酒和婴儿食品)中发现的最常见的霉菌毒素。据报道,接触这种霉菌毒素会导致肠道和肾脏损伤。本研究调查了PAT诱导人结肠癌细胞(HCT116)和胚胎肾细胞(HEK293)毒性的机制。我们证明,PAT激活了内质网(ER)和未折叠蛋白反应,这可通过GRP78和GADD34的上调、XBP1 mRNA的剪接以及促凋亡因子CHOP的表达来证明。这种内质网应激反应伴随着线粒体凋亡途径的诱导。细胞凋亡伴随着活性氧的产生、线粒体膜电位的下降和半胱天冬酶的激活。此外,我们表明促凋亡蛋白Bax或Bak的缺失可保护细胞免受PAT诱导的凋亡。用活性氧清除剂N - 乙酰半胱氨酸处理细胞可抑制内质网应激反应并防止线粒体凋亡。总的来说,我们的数据为PAT诱导的细胞死亡信号通路提供了新的机制见解,并证明PAT通过一种依赖活性氧的机制诱导细胞毒性,该机制涉及内质网应激和人肠道及肾细胞中线粒体凋亡途径的激活。