用于动态结构亚细胞成像的非相干彩色全息点阵光片

Simon Alford, C. Mann, Jonathan Art, M. Potcoava
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引用次数: 1

摘要

本文的目的是探索使用非相干彩色全息晶格光片(ICHLLS)对活体组织中的三维细胞动力学进行多波长定量监测的必要性和优势,以进一步了解细胞和细胞隔室的复杂功能。我们已经探索了使用非相干彩色全息术晶格光片来研究完整组织中活细胞中荧光标记物的共定位。神经元结构为非相干彩色全息点阵光片提供了一个有吸引力的靶点。细胞在3D空间中显示出复杂的结构,其中细胞之间和亚细胞结构内的信号传导需要蛋白质和脂质的共定位才能发挥作用。在活动期间和长时间内,了解完整组织中活细胞内帕金森氏症、阿尔茨海默氏症和运动神经元疾病的这些信号功能非常重要。作为概念验证,本文回顾了晶格光片成像的关键方面,并描述了非相干检测系统配置,以主动控制双衍射透镜在多个激发波长下的相移,并按每个z-galvo扫描级别扩展视野。非相干彩色全息术晶格光片系统将允许同时记录包含三维空间强度、相位和波长信息的多维物体波。我们测量引入完整神经组织中活细胞的荧光指示剂的共定位。
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Incoherent color holography lattice light-sheet for subcellular imaging of dynamic structures
The purpose of the article is to explore the need and advantages of using the incoherent color holography lattice light-sheet (ICHLLS) to provide multiwavelength quantitative monitoring of 3D cellular dynamics in live tissue to further understand complex functions of cells and cellular compartments. We have explored the use of incoherent color holography lattice light-sheet to investigate colocalization of fluorescent markers in live cells in intact tissue. Neuronal structures provide an attractive target for incoherent color holography lattice light-sheet. The cells show a complex architecture in 3D space in which signaling both between cells and within subcellular structures requires colocalization of proteins and lipids to function. During activity and over long periods it is important in understanding these signaling functions in Parkinson’s, Alzheimer’s and motoneuron diseases within live cells in intact tissue. As a proof of concept this article recalls the key aspects in lattice light-sheet imaging and provides a description of the incoherent detection system configuration to actively control dual diffractive lenses phase-shifting at multiple excitation wavelengths sequentially, and per each z-galvo scanning level, with extended field-of-view. The incoherent color holography lattice light-sheet system will allow simultaneous recording of multidimensional object waves that contain intensity in 3D space, phase, and wavelength information. We measure colocalization of fluorescence indicators introduced into live cells in intact neural tissue.
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