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用于耗氧量和乳酸生成分析的胰腺腺泡细胞制备

Pancreatic Acinar Cell Preparation for Oxygen Consumption and Lactate Production Analysis.

作者信息

Armstrong Jane A, Sutton Robert, Criddle David N

机构信息

Department of Clinical Cancer Medicine, Institute of Translational Medicine, University of Liverpool, UK.

Department of Molecular and Cellular Physiology, Institute of Translational Medicine, University of Liverpool, UK.

出版信息

Bio Protoc. 2020 May 20;10(10):e3627. doi: 10.21769/BioProtoc.3627.

Abstract

Mitochondrial dysfunction is a principal feature of acute pancreatitis (AP) although the underlying mechanisms are still unclear. AP precipitants induce Ca-dependent formation of the mitochondrial permeability transition pore (MPTP) in pancreatic acinar cells (PACs), leading to ATP depletion and necrosis. Evaluations of mitochondrial bioenergetics have mainly been performed in isolated PACs using confocal microscopy, with assessment of mitochondrial membrane potential, NADH/FAD and ATP levels, coupled with patch-clamp electrophysiology. These studies are technically demanding and time-consuming. Application of Seahorse flux analysis now allows detailed investigations of bioenergetics changes to be performed in cell populations using a multi-well plate-reader format; rates of oxygen consumption (OCR) and extracellular acidification (ECAR) provide important information about cellular respiration and glycolysis, respectively. Parameters such as maximal respiration, ATP-linked capacity and proton leak can be derived from application of a respiratory function "stress" test that involves pharmacological manipulation of the electron transport chain. The use of Seahorse Flux analysis therefore provides a quick, and convenient means to measure detailed cellular bioenergetics and allows results to be coupled with other plate-reader based assays, providing a fuller understanding of the pathophysiological consequences of mitochondrial bioenergetics alterations.

摘要

线粒体功能障碍是急性胰腺炎(AP)的一个主要特征,尽管其潜在机制仍不清楚。AP诱发因素可导致胰腺腺泡细胞(PACs)中钙依赖性线粒体通透性转换孔(MPTP)的形成,进而导致ATP耗竭和坏死。线粒体生物能量学的评估主要是在分离的PACs中使用共聚焦显微镜进行的,评估线粒体膜电位、NADH/FAD和ATP水平,并结合膜片钳电生理学。这些研究技术要求高且耗时。现在,海马通量分析的应用使得能够使用多孔板读数器以细胞群体为对象详细研究生物能量学变化;耗氧率(OCR)和细胞外酸化率(ECAR)分别提供了有关细胞呼吸和糖酵解的重要信息。诸如最大呼吸、ATP关联能力和质子泄漏等参数可以通过应用涉及对电子传递链进行药理学操作的呼吸功能“应激”试验得出。因此,使用海马通量分析提供了一种快速、便捷的方法来测量详细的细胞生物能量学,并使结果能够与其他基于板读数器的检测方法相结合,从而更全面地了解线粒体生物能量学改变的病理生理后果。

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