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实时研究具有不同视场和分辨率的活体生物样本中生理活动的时空动态(4D)。

Real-time study of spatio-temporal dynamics (4D) of physiological activities in alive biological specimens with different FOVs and resolutions simultaneously.

机构信息

School of Physics (SoP), Indian Institute of Science Education and Research Thiruvananthapuram (IISER TVM), Thiruvananthapuram, Kerala, 695551, India.

School of Biology (SoB), Indian Institute of Science Education and Research Thiruvananthapuram (IISER TVM), Thiruvananthapuram, Kerala, 695551, India.

出版信息

Sci Rep. 2024 Feb 12;14(1):3542. doi: 10.1038/s41598-024-52152-x.

Abstract

This article reports the development of a microscopy imaging system that gives feasibility for studying spatio-temporal dynamics of physiological activities of alive biological specimens (over entire volume not only for a particular section, i.e., in 4D). The imaging technology facilitates to obtain two image frames of a section of the larger specimen ([Formula: see text]) with different FOVs at different resolutions or magnifications simultaneously in real-time (in addition to recovery of 3D (volume) information). Again, this imaging system addresses the longstanding challenges of housing multiple light sources (6 at the maximum till date) in microscopy (in general) and light sheet fluorescence microscopy (LSFM) (in particular), by using a tuneable pulsed laser source (with an operating wavelength in the range [Formula: see text]-670 nm) in contrast to the conventional CW laser source being adopted for inducing photo-excitation of tagged fluorophores. In the present study, we employ four wavelengths ([Formula: see text] 488 nm, 585 nm, 590 nm, and 594 nm). Our study also demonstrates quantitative characterization of spatio-temporal dynamics (velocity-both amplitude and direction) of organelles (mitochondria) and their mutual correlationships. Mitochondria close to the nucleus (or in clustered cells) are observed to possess a lower degree of freedom in comparison to that at the cellular periphery (or isolated cells). In addition, the study demonstrates real-time observation and recording of the development and growth of all tracheal branches during the entire period ([Formula: see text] min) of embryonic development (Drosophila). The experimental results-with experiments being conducted in various and diversified biological specimens (Drosophila melanogaster, mouse embryo, and HeLa cells)-demonstrate that the study is of great scientific impact both from the aspects of technology and biological sciences.

摘要

本文报道了一种显微镜成像系统的开发,该系统为研究活生物标本(不仅是特定部分,即整个体积,而且是整个体积)的生理活动的时空动态提供了可行性。该成像技术能够实时(除了恢复 3D(体积)信息外)同时获得较大标本的一个部分的两个图像帧,这两个图像帧具有不同的视场(FOV)和不同的分辨率或放大倍数。同样,该成像系统通过使用可调谐脉冲激光源(工作波长范围为[Formula: see text]-670nm)解决了在显微镜(一般而言)和光片荧光显微镜(LSFM)(特别是)中容纳多个光源(迄今为止最多 6 个)的长期挑战,与用于诱导标记荧光团光激发的传统连续波激光源形成对比。在本研究中,我们使用了四个波长([Formula: see text]488nm、585nm、590nm 和 594nm)。我们的研究还演示了细胞器(线粒体)时空动态(幅度和方向的速度)的定量表征及其相互关系。与细胞边缘(或孤立细胞)相比,靠近细胞核(或聚集细胞)的线粒体具有较低的自由度。此外,该研究还演示了在胚胎发育(果蝇)的整个时期([Formula: see text]min)内对所有气管分支的发育和生长进行实时观察和记录。在各种和多样化的生物标本(黑腹果蝇、小鼠胚胎和 HeLa 细胞)中进行实验的实验结果表明,从技术和生物科学两个方面来看,这项研究都具有重大的科学影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/889f/10861542/732b882322e4/41598_2024_52152_Fig1_HTML.jpg

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