Intravital imaging with two-photon microscopy reveals cellular dynamics in the ischeamia-reperfused rat heart

被引:0
作者
Ryohei Matsuura
Shigeru Miyagawa
Satsuki Fukushima
Takasumi Goto
Akima Harada
Yuri Shimozaki
Kazumasa Yamaki
Sho Sanami
Junichi Kikuta
Masaru Ishii
Yoshiki Sawa
机构
[1] Osaka University Graduate School of Medicine,Department of Cardiovascular Surgery
[2] Osaka University Graduate School of Medicine,Department of Immunology and Cell Biology
[3] Research and Development Center,Research and Development Division for Advanced Technology
[4] Dai Nippon Printing Co.,undefined
[5] Ltd.,undefined
来源
Scientific Reports | / 8卷
关键词
Intravital Imaging; Transgenic Lewis Rats; Heart Beating; Dynamic Biological Events; Intravital Microscopy System;
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摘要
Recent advances in intravital microscopy have provided insight into dynamic biological events at the cellular level in both healthy and pathological tissue. However, real-time in vivo cellular imaging of the beating heart has not been fully established, mainly due to the difficulty of obtaining clear images through cycles of cardiac and respiratory motion. Here we report the successful recording of clear in vivo moving images of the beating rat heart by two-photon microscopy facilitated by cardiothoracic surgery and a novel cardiac stabiliser. Subcellular dynamics of the major cardiac components including the myocardium and its subcellular structures (i.e., nuclei and myofibrils) and mitochondrial distribution in cardiac myocytes were visualised for 4–5 h in green fluorescent protein-expressing transgenic Lewis rats at 15 frames/s. We also observed ischaemia/reperfusion (I/R) injury-induced suppression of the contraction/relaxation cycle and the consequent increase in cell permeability and leukocyte accumulation in cardiac tissue. I/R injury was induced in other transgenic mouse lines to further clarify the biological events in cardiac tissue. This imaging system can serve as an alternative modality for real time monitoring in animal models and cardiological drug screening, and can contribute to the development of more effective treatments for cardiac diseases.
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[1]  
Ishii M(2009)Sphingosine-1-phosphate mobilizes osteoclast precursors and regulates bone homeostasis Nature 458 524-528
[2]  
Kikuta J(2013)Dynamic visualization of RANKL and Th17-mediated osteoclast function J. Clin. Invest. 123 866-873
[3]  
Sekimoto R(2015)Visualized macrophage dynamics and significance of S100A8 in obese fat Proc. Natl Acad. Sci. USA 112 E2058-E2066
[4]  
Nishikawa K(2015)DNA methyltransferase 3a regulates osteoclast differentiation by coupling to an S-adenosylmethionine-producing metabolic pathway Nat. Med. 21 281-287
[5]  
Pittet MJ(2011)Intravital imaging Cell 147 983-991
[6]  
Weissleder R(1990)Two-photon laser scanning fluorescence microscopy Science 248 73-76
[7]  
Denk W(2004)Two-photon microscopy of cells and tissue Circ Res. 95 1154-1166
[8]  
Strickler JH(2013)Fast measurement of sarcomere length and cell orientation in Langendorff-perfused hearts using remote focusing microscopy Circ. Res. 113 863-870
[9]  
Webb WW(2010)Measurement and analysis of sarcomere length in rat cardiomyocytes Am. J. Physiol. Heart Circ. Physiol. 298 H1616-H1625
[10]  
Rubart M(1998) and Cell Signal. 10 331-337