Real-time luminescence imaging of cellular ATP release

被引:29
作者
Furuya, Kishio [1 ,2 ]
Sokabe, Masahiro [1 ]
Grygorczyk, Ryszard [1 ,3 ,4 ]
机构
[1] Nagoya Univ, Grad Sch Med, Dept Physiol, Nagoya, Aichi 4668550, Japan
[2] Nagoya Univ, FIRST Res Ctr Innovat Nanobiodevices, Nagoya, Aichi 4668550, Japan
[3] Univ Montreal, Hotel Dieu, Ctr Hosp Univ Montreal CRCHUM, Res Ctr, Montreal, PQ, Canada
[4] Univ Montreal, Dept Med, Montreal, PQ H3C 3J7, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院; 日本学术振兴会;
关键词
Luminescence microscopy; Luciferin-luciferase; ATP release; Mechanical stimulation; Infra-red imaging; Hypotonic stress; SUBEPITHELIAL FIBROBLASTS; CA2+; VISUALIZATION; OSCILLATIONS; INVOLVEMENT; RECEPTORS; RESPONSES; ROLES; CELLS; WAVES;
D O I
10.1016/j.ymeth.2013.08.007
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Extracellular ATP and other purines are ubiquitous mediators of local intercellular signaling within the body. While the last two decades have witnessed enormous progress in uncovering and characterizing purinergic receptors and extracellular enzymes controlling purinergic signals, our understanding of the initiating step in this cascade, i.e., ATP release, is still obscure. Imaging of extracellular ATP by luciferin-luciferase bioluminescence offers the advantage of studying ATP release and distribution dynamics in real time. However, low-light signal generated by bioluminescence reactions remains the major obstacle to imaging such rapid processes, imposing substantial constraints on its spatial and temporal resolution. We have developed an improved microscopy system for real-time ATP imaging, which detects ATP-dependent luciferin-luciferase luminescence at similar to 10 frames/s, sufficient to follow rapid ATP release with sensitivity of similar to 10 nM and dynamic range up to 100 mu M. In addition, simultaneous differential interference contrast cell images are acquired with infra-red optics. Our imaging method: (1) identifies ATP-releasing cells or sites, (2) determines absolute ATP concentration and its spreading manner at release sites, and (3) permits analysis of ATP release kinetics from single cells. We provide instrumental details of our approach and give several examples of ATP-release imaging at cellular and tissue levels, to illustrate its potential utility. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:330 / 344
页数:15
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