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使用基因编码探针进行小鼠氧化还原组织学研究。

Mouse redox histology using genetically encoded probes.

作者信息

Fujikawa Yuuta, Roma Leticia P, Sobotta Mirko C, Rose Adam J, Diaz Mauricio Berriel, Locatelli Giuseppe, Breckwoldt Michael O, Misgeld Thomas, Kerschensteiner Martin, Herzig Stephan, Müller-Decker Karin, Dick Tobias P

机构信息

Division of Redox Regulation, DKFZ-ZMBH (German Cancer Research Center-Center for Molecular Biology of the University of Heidelberg) Alliance, DKFZ, Im Neuenheimer Feld 280, 69120 Heidelberg, Germany.

Joint Division Molecular Metabolic Control, DKFZ-ZMBH Alliance, DKFZ Heidelberg, Center for Molecular Biology (ZMBH) and University Hospital, University of Heidelberg, 69120 Heidelberg, Germany.

出版信息

Sci Signal. 2016 Mar 15;9(419):rs1. doi: 10.1126/scisignal.aad3895.

Abstract

Mapping the in vivo distribution of endogenous oxidants in animal tissues is of substantial biomedical interest. Numerous health-related factors, including diet, physical activity, infection, aging, toxins, or pharmacological intervention, may cause redox changes. Tools are needed to pinpoint redox state changes to particular organs, tissues, cell types, and subcellular organelles. We describe a procedure that preserves the in vivo redox state of genetically encoded redox biosensors within histological tissue sections, thus providing "redox maps" for any tissue and comparison of interest. We demonstrate the utility of the technique by visualizing endogenous redox differences and changes in the context of tumor growth, inflammation, embryonic development, and nutrient starvation.

摘要

绘制动物组织中内源性氧化剂的体内分布图具有重大的生物医学意义。许多与健康相关的因素,包括饮食、体育活动、感染、衰老、毒素或药物干预,都可能导致氧化还原变化。需要工具来确定特定器官、组织、细胞类型和亚细胞器的氧化还原状态变化。我们描述了一种在组织学组织切片中保存基因编码氧化还原生物传感器体内氧化还原状态的方法,从而为任何感兴趣的组织和比较提供“氧化还原图谱”。我们通过在肿瘤生长、炎症、胚胎发育和营养饥饿的背景下可视化内源性氧化还原差异和变化来证明该技术的实用性。

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