IMART software for correction of motion artifacts in images collected in intravital microscopy.

IntraVital Pub Date : 2014-01-01 DOI:10.4161/intv.28210
Kenneth W Dunn, Kevin S Lorenz, Paul Salama, Edward J Delp
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引用次数: 23

Abstract

Intravital microscopy is a uniquely powerful tool, providing the ability to characterize cell and organ physiology in the natural context of the intact, living animal. With the recent development of high-resolution microscopy techniques such as confocal and multiphoton microscopy, intravital microscopy can now characterize structures at subcellular resolution and capture events at sub-second temporal resolution. However, realizing the potential for high resolution requires remarkable stability in the tissue. Whereas the rigid structure of the skull facilitates high-resolution imaging of the brain, organs of the viscera are free to move with respiration and heartbeat, requiring additional apparatus for immobilization. In our experience, these methods are variably effective, so that many studies are compromised by residual motion artifacts. Here we demonstrate the use of IMART, a software tool for removing motion artifacts from intravital microscopy images collected in time series or in three dimensions.

Abstract Image

Abstract Image

Abstract Image

用于校正活体显微术中采集的图像中的运动伪影的IMART软件。
活体显微镜是一种独特的强大工具,提供了在完整的、活的动物的自然环境中表征细胞和器官生理学的能力。随着高分辨率显微镜技术的发展,如共聚焦显微镜和多光子显微镜,活体显微镜现在可以在亚细胞分辨率下表征结构,并在亚秒时间分辨率下捕获事件。然而,实现高分辨率的潜力需要在组织中具有显著的稳定性。尽管颅骨的刚性结构有利于大脑的高分辨率成像,但内脏器官可以随呼吸和心跳自由运动,需要额外的固定装置。根据我们的经验,这些方法的效果各不相同,因此许多研究都受到残余运动伪影的影响。在这里,我们演示了使用IMART,这是一种软件工具,用于从时间序列或三维空间收集的活体显微镜图像中去除运动伪影。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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