Intravital imaging of cardiac function at the single-cell level

被引:53
作者
Aguirre, Aaron D. [1 ,2 ]
Vinegoni, Claudio [1 ]
Sebas, Matt [1 ]
Weissleder, Ralph [1 ,3 ]
机构
[1] Massachusetts Gen Hosp, Ctr Syst Biol, Boston, MA 02114 USA
[2] Brigham & Womens Hosp, Dept Med, Div Cardiovasc, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
intravital micoscopy; molecular imaging; cardiovascular imaging; fluorescence; pacing; IN-SITU; SARCOMERE-LENGTH; 2-PHOTON MICROSCOPY; MURINE HEART; MOUSE HEARTS; RAT-HEART; LANGENDORFF; CARDIOMYOCYTES; PRESSURE; TENSION;
D O I
10.1073/pnas.1401316111
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Knowledge of cardiomyocyte biology is limited by the lack of methods to interrogate single-cell physiology in vivo. Here we show that contracting myocytes can indeed be imaged with optical microscopy at high temporal and spatial resolution in the beating murine heart, allowing visualization of individual sarcomeres and measurement of the single cardiomyocyte contractile cycle. Collectively, this has been enabled by efficient tissue stabilization, a prospective real-time cardiac gating approach, an image processing algorithm for motion-artifact-free imaging throughout the cardiac cycle, and a fluorescent membrane staining protocol. Quantification of cardiomyocyte contractile function in vivo opens many possibilities for investigating myocardial disease and therapeutic intervention at the cellular level.
引用
收藏
页码:11257 / 11262
页数:6
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