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Imaging the beating heart in the mouse using intravital microscopy techniques

Authors
Vinegoni, ClaudioAguirre, Aaron D.Lee, SungonWeissleder, Ralph
Issue Date
Nov-2015
Publisher
NATURE PUBLISHING GROUP
Keywords
IN-VIVO; CARDIAC-FUNCTION; BLOOD-FLOW; MOTION; MODELS; CELLS; MICE
Citation
NATURE PROTOCOLS, v.10, no.11, pp.1802 - 1819
Indexed
SCIE
SCOPUS
Journal Title
NATURE PROTOCOLS
Volume
10
Number
11
Start Page
1802
End Page
1819
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/16580
DOI
10.1038/nprot.2015.119
ISSN
1754-2189
Abstract
Real-time microscopic imaging of moving organs at single-cell resolution represents a major challenge in studying complex biology in living systems. Motion of the tissue from the cardiac and respiratory cycles severely limits intravital microscopy by compromising ultimate spatial and temporal imaging resolution. However, significant recent advances have enabled single-cell resolution imaging to be achieved in vivo. In this protocol, we describe experimental procedures for intravital microscopy based on a combination of thoracic surgery, tissue stabilizers and acquisition gating methods, which enable imaging at the single-cell level in the beating heart in the mouse. Setup of the model is typically completed in 1 h, which allows 2 h or more of continuous cardiac imaging. This protocol can be readily adapted for the imaging of other moving organs, and it will therefore broadly facilitate in vivo high-resolution microscopy studies.
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ERICA 공학대학 (DEPARTMENT OF ROBOT ENGINEERING)
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