4.6 Article

Five-dimensional two-photon volumetric microscopy of in-vivo dynamic activities using liquid lens remote focusing

期刊

BIOMEDICAL OPTICS EXPRESS
卷 10, 期 7, 页码 3591-3604

出版社

OPTICAL SOC AMER
DOI: 10.1364/BOE.10.003591

关键词

-

资金

  1. National Science Foundation [1706916]
  2. National Institutes of Health [R21EB027802]
  3. Center for Regenerative Engineering and Medicine (REM)
  4. Soft Bones Foundation
  5. Div Of Chem, Bioeng, Env, & Transp Sys
  6. Directorate For Engineering [1706916] Funding Source: National Science Foundation

向作者/读者索取更多资源

Multi-photon scanning microscopy provides a robust tool for optical sectioning, which can be used to capture fast biological events such as blood flow, mitochondrial activity, and neuronal action potentials. For many studies, it is important to visualize several different focal planes at a rate akin to the biological event frequency. Typically, a microscope is equipped with mechanical elements to move either the sample or the objective lens to capture volumetric information, but these strategies are limited due to their slow speeds or inertial artifacts. To overcome this problem, remote focusing methods have been developed to shift the focal plane axially without physical movement of the sample or the microscope. Among these methods is liquid lens technology, which adjusts the focus of the lens by changing the wettability of the liquid and hence its curvature. Liquid lenses are inexpensive active optical elements that have the potential for fast multi-photon volumetric imaging. hence a promising and accessible approach for the study of biological systems with complex dynamics Although remote focusing using liquid lens technology can be used for volumetric point scanning multi-photon microscopy, optical aberrations and the effects of high energy laser pulses have been concerns in its implementation. In this paper, we characterize a liquid lens and validate its use in relevant biological applications. We measured optical aberrations that are caused by the liquid lens, and calculated its response time, defocus hysteresis. and thermal response to a pulsed laser. We applied this method of remote focusing for imaging and measurement of multiple in-vivo specimens, including mesenchymal stem cell dynamics, mouse tibialis anterior muscle mitochondrial electrical potential fluctuations, and mouse brain neural activity. Our system produces 5 dimensional (x,y,z,lambda,t) data sets at the speed of 4.2 volumes per second over volumes as large as 160 x 160 x 35 mu m(3). (C) 2019 Optical Society of America under the terms of the OSA Open Access Publishing Agreement

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据