College of Nursing, Biobehavioral Healthscience Division & College of Medicine, Department of Medicine Division of Translational & Regenerative Medicine, The University of Arizona, Tucson, Arizona.
Department of Physiological Sciences and Center for Environmental and Human Toxicology, University of Florida, Gainesville, Florida.
J Cell Biochem. 2018 Jan;119(1):599-606. doi: 10.1002/jcb.26219. Epub 2017 Sep 11.
Exosomes are nano-sized vesicles that are secreted into the extracellular environment. These vesicles contain various biological effector molecules that can regulate intracellular signaling pathways in recipient cells. The aim of this study was to examine a correlation between exosomal cathepsin B activity and the receptor for advanced glycation end-products (RAGE). Type 1 alveolar epithelial (R3/1) cells were treated with or without hydrogen peroxide and exosomes isolated from the cell conditioned media were characterized by NanoSight analysis. Lipidomic and proteomic analysis showed exosomes released from R3/1 cells exposed to oxidative stress induced by hydrogen peroxide or vehicle differ in their lipid and protein content, respectively. Cathepsin B activity was detected in exosomes isolated from hydrogen peroxide treated cells. The mRNA and protein expression of RAGE increased in cultured R3/1 cells treated with exosomes containing active cathepsin B while depletion of exosomal cathepsin B attenuated RAGE mRNA and protein expression. These results suggest exosomal cathepsin B regulates RAGE in type 1 alveolar cells under conditions of oxidative stress. J. Cell. Biochem. 119: 599-606, 2018. © 2017 Wiley Periodicals, Inc.
外泌体是分泌到细胞外环境中的纳米大小的囊泡。这些囊泡包含各种生物效应分子,可以调节受体细胞内的信号通路。本研究旨在探讨外泌体组织蛋白酶 B 活性与晚期糖基化终产物受体 (RAGE) 之间的相关性。用或不用过氧化氢处理 1 型肺泡上皮 (R3/1) 细胞,并通过纳米视分析对细胞条件培养基中分离的外泌体进行特征分析。脂质组学和蛋白质组学分析表明,来自暴露于过氧化氢或载体诱导的氧化应激的 R3/1 细胞释放的外泌体在其脂质和蛋白质含量上存在差异。在含有活性组织蛋白酶 B 的外泌体处理的细胞中检测到组织蛋白酶 B 活性。含有活性组织蛋白酶 B 的外泌体处理的培养 R3/1 细胞中 RAGE 的 mRNA 和蛋白表达增加,而外泌体组织蛋白酶 B 的耗竭则减弱了 RAGE 的 mRNA 和蛋白表达。这些结果表明,在氧化应激条件下,外泌体组织蛋白酶 B 调节 1 型肺泡细胞中的 RAGE。J. 细胞。生化学。119:599-606,2018。©2017 年 Wiley Periodicals, Inc.