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监测和比较线粒体与糖酵解ATP生成的方法。

Methods to monitor and compare mitochondrial and glycolytic ATP production.

作者信息

Patergnani Simone, Baldassari Federica, De Marchi Elena, Karkucinska-Wieckowska Agnieszka, Wieckowski Mariusz R, Pinton Paolo

机构信息

Section of Pathology, Oncology and Experimental Biology, Laboratory for Technologies of Advanced Therapies (LTTA), Department of Morphology, Surgery and Experimental Medicine, Ferrara, Italy.

Department of Pathology, The Children's Memorial Health Institute, Warsaw, Poland.

出版信息

Methods Enzymol. 2014;542:313-32. doi: 10.1016/B978-0-12-416618-9.00016-9.

Abstract

ATP is commonly considered as the main energy unit of the cell and participates in a variety of cellular processes. Thus, intracellular ATP concentrations rapidly vary in response to a wide variety of stimuli, including nutrients, hormones, cytotoxic agents, and hypoxia. Such alterations not necessarily affect cytosolic and mitochondrial ATP to similar extents. From an oncological perspective, this is particularly relevant in the course of tumor progression as well as in the response of cancer cells to therapy. In normal cells, mitochondrial oxidative phosphorylation (OXPHOS) is the predominant source of ATP. Conversely, many cancer cells exhibit an increased flux through glycolysis irrespective of oxygen tension. Assessing the relative contribution of glycolysis and OXPHOS to intracellular ATP production is fundamental not only for obtaining further insights into the peculiarities and complexities of oncometabolism but also for developing therapeutic and diagnostic tools. Several techniques have been developed to measure intracellular ATP levels including enzymatic methods based on hexokinase, glucose-6-phosphate dehydrogenase, and firefly luciferase. Here, we summarize conventional methods for measuring intracellular ATP levels and we provide a detailed protocol based on cytosol- and mitochondrion-targeted variants of firefly luciferase to determine the relative contribution of glycolysis and OXPHOS to ATP synthesis.

摘要

三磷酸腺苷(ATP)通常被认为是细胞的主要能量单位,并参与多种细胞过程。因此,细胞内ATP浓度会因各种刺激而迅速变化,这些刺激包括营养物质、激素、细胞毒性剂和缺氧。这种变化不一定会对细胞质和线粒体中的ATP产生相似程度的影响。从肿瘤学角度来看,这在肿瘤进展过程以及癌细胞对治疗的反应中尤为重要。在正常细胞中,线粒体氧化磷酸化(OXPHOS)是ATP的主要来源。相反,许多癌细胞无论氧张力如何,都表现出糖酵解通量增加。评估糖酵解和氧化磷酸化对细胞内ATP产生的相对贡献不仅对于深入了解肿瘤代谢的特殊性和复杂性至关重要,而且对于开发治疗和诊断工具也很重要。已经开发了几种技术来测量细胞内ATP水平,包括基于己糖激酶、葡萄糖-6-磷酸脱氢酶和萤火虫荧光素酶的酶促方法。在这里,我们总结了测量细胞内ATP水平的传统方法,并提供了一个基于萤火虫荧光素酶的细胞质和线粒体靶向变体的详细方案,以确定糖酵解和氧化磷酸化对ATP合成的相对贡献。

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