• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

用于快速体积成像的双光子激光扫描体视显微镜

Two-Photon Laser Scanning Stereomicroscopy for Fast Volumetric Imaging.

作者信息

Yang Yanlong, Yao Baoli, Lei Ming, Dan Dan, Li Runze, Horn Mark Van, Chen Xun, Li Yang, Ye Tong

机构信息

State Key Laboratory of Transient Optics and Photonics, Xi'an Institute of Optics and Precision Mechanics, Chinese Academy of Sciences, Xi'an, China.

Department of Radiology, Medical University of South Carolina, Charleston, South Carolina, United States of America.

出版信息

PLoS One. 2016 Dec 20;11(12):e0168885. doi: 10.1371/journal.pone.0168885. eCollection 2016.

DOI:10.1371/journal.pone.0168885
PMID:27997624
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5173245/
Abstract

Bessel beams have been successfully used in two-photon laser scanning fluorescence microscopy to extend the depth of field (EDF), which makes it possible to observe fast events volumetrically. However, the depth information is lost due to integration of fluorescence signals along the propagation direction. We describe the design and implementation of two-photon lasers scanning stereomicroscopy, which allows viewing dynamic processes in three-dimensional (3D) space stereoscopically in real-time with shutter glasses at the speed of 1.4 volumes per second. The depth information can be appreciated by human visual system or be recovered with correspondence algorithms for some cases.

摘要

贝塞尔光束已成功应用于双光子激光扫描荧光显微镜中以扩展景深(EDF),这使得对快速事件进行体视观察成为可能。然而,由于荧光信号沿传播方向的积分,深度信息会丢失。我们描述了双光子激光扫描体视显微镜的设计与实现,它允许使用快门眼镜以每秒1.4个容积的速度实时立体地观察三维(3D)空间中的动态过程。深度信息可以被人类视觉系统感知,或者在某些情况下通过对应算法恢复。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ce/5173245/348c3bd8f23a/pone.0168885.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ce/5173245/7a0bf25a2170/pone.0168885.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ce/5173245/ad2caa5190ea/pone.0168885.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ce/5173245/45b298127d20/pone.0168885.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ce/5173245/67be81ec8c06/pone.0168885.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ce/5173245/f16e325d1705/pone.0168885.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ce/5173245/46c16d434b7d/pone.0168885.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ce/5173245/348c3bd8f23a/pone.0168885.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ce/5173245/7a0bf25a2170/pone.0168885.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ce/5173245/ad2caa5190ea/pone.0168885.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ce/5173245/45b298127d20/pone.0168885.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ce/5173245/67be81ec8c06/pone.0168885.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ce/5173245/f16e325d1705/pone.0168885.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ce/5173245/46c16d434b7d/pone.0168885.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ce/5173245/348c3bd8f23a/pone.0168885.g007.jpg

相似文献

1
Two-Photon Laser Scanning Stereomicroscopy for Fast Volumetric Imaging.用于快速体积成像的双光子激光扫描体视显微镜
PLoS One. 2016 Dec 20;11(12):e0168885. doi: 10.1371/journal.pone.0168885. eCollection 2016.
2
Light-sheet microscopy by confocal line scanning of dual-Bessel beams.通过双贝塞尔光束的共焦线扫描进行光片显微镜成像。
J Biomed Opt. 2016 Oct 1;21(10):100502. doi: 10.1117/1.JBO.21.10.100502.
3
A line scanning confocal fluorescent microscope using a CMOS rolling shutter as an adjustable aperture.使用 CMOS 卷帘快门作为可调孔径的线扫描共聚焦荧光显微镜。
J Microsc. 2012 Sep;247(3):269-76. doi: 10.1111/j.1365-2818.2012.03642.x.
4
Three dimensional sidewall measurements by laser fluorescent confocal microscopy.通过激光荧光共聚焦显微镜进行三维侧壁测量。
Opt Express. 2008 Mar 17;16(6):4001-14. doi: 10.1364/oe.16.004001.
5
A compact Acousto-Optic Lens for 2D and 3D femtosecond based 2-photon microscopy.一种用于基于飞秒的二维和三维双光子显微镜的紧凑型声光透镜。
Opt Express. 2010 Jun 21;18(13):13721-45. doi: 10.1364/OE.18.013720.
6
Volumetric two-photon imaging of neurons using stereoscopy (vTwINS).使用体视学的容积双光子显微镜成像神经元(vTwINS)。
Nat Methods. 2017 Apr;14(4):420-426. doi: 10.1038/nmeth.4226. Epub 2017 Mar 20.
7
Self-interference fluorescence microscopy: three dimensional fluorescence imaging without depth scanning.自干涉荧光显微镜:无需深度扫描的三维荧光成像。
Opt Express. 2012 Jul 2;20(14):15253-62. doi: 10.1364/OE.20.015253.
8
Single-photon-counting detector for increased sensitivity in two-photon laser scanning microscopy.用于提高双光子激光扫描显微镜灵敏度的单光子计数探测器。
Opt Lett. 2008 Dec 15;33(24):2895-7. doi: 10.1364/ol.33.002895.
9
High speed two-photon laser scanning stereomicroscopy for three-dimension tracking multiple particles simultaneously in three-dimension.用于在三维空间中同时三维跟踪多个粒子的高速双光子激光扫描立体显微镜。
Front Photon. 2022;3. doi: 10.3389/fphot.2022.985474. Epub 2022 Sep 6.
10
Low-invasive 5D visualization of mitotic progression by two-photon excitation spinning-disk confocal microscopy.双光子激发旋转盘共聚焦显微镜的低侵入性 5D 有丝分裂进程可视化。
Sci Rep. 2022 Jan 17;12(1):809. doi: 10.1038/s41598-021-04543-7.

引用本文的文献

1
An updated narrative review on revolutionizing erectile dysfunction treatment: the crucial role of trophic factors in Adipose-Derived stem cell therapy.关于革新勃起功能障碍治疗的最新叙述性综述:营养因子在脂肪干细胞治疗中的关键作用。
BMC Urol. 2025 Aug 19;25(1):206. doi: 10.1186/s12894-025-01861-0.
2
High speed two-photon laser scanning stereomicroscopy for three-dimension tracking multiple particles simultaneously in three-dimension.用于在三维空间中同时三维跟踪多个粒子的高速双光子激光扫描立体显微镜。
Front Photon. 2022;3. doi: 10.3389/fphot.2022.985474. Epub 2022 Sep 6.
3
Three-photon excited fluorescence imaging in neuroscience: From principles to applications.

本文引用的文献

1
TrackMate: An open and extensible platform for single-particle tracking.TrackMate:一个用于单粒子追踪的开放且可扩展的平台。
Methods. 2017 Feb 15;115:80-90. doi: 10.1016/j.ymeth.2016.09.016. Epub 2016 Oct 3.
2
Technologies for imaging neural activity in large volumes.用于对大量神经活动进行成像的技术。
Nat Neurosci. 2016 Aug 26;19(9):1154-64. doi: 10.1038/nn.4358.
3
Continuous volumetric imaging via an optical phase-locked ultrasound lens.通过光学锁相超声透镜进行连续体积成像。
神经科学中的三光子激发荧光成像:从原理到应用
Front Neurosci. 2023 Feb 20;17:1085682. doi: 10.3389/fnins.2023.1085682. eCollection 2023.
4
Depth random-access two-photon Bessel light-sheet imaging in brain tissue.脑组织中深度随机访问双光子贝塞尔光片成像。
Opt Express. 2022 Jul 18;30(15):26396-26406. doi: 10.1364/OE.456871.
5
High-speed volumetric two-photon fluorescence imaging of neurovascular dynamics.高速容积双光子荧光成像技术用于神经血管动力学研究。
Nat Commun. 2020 Nov 26;11(1):6020. doi: 10.1038/s41467-020-19851-1.
Nat Methods. 2015 Aug;12(8):759-62. doi: 10.1038/nmeth.3476. Epub 2015 Jul 13.
4
Whole-brain functional imaging with two-photon light-sheet microscopy.采用双光子光片显微镜进行全脑功能成像。
Nat Methods. 2015 May;12(5):379-80. doi: 10.1038/nmeth.3371.
5
Non-descanned multifocal multiphoton microscopy with a multianode photomultiplier tube.配备多阳极光电倍增管的非扫描多焦点多光子显微镜。
AIP Adv. 2015 Mar 23;5(8):084802. doi: 10.1063/1.4916040. eCollection 2015 Aug.
6
Extended two-photon microscopy in live samples with Bessel beams: steadier focus, faster volume scans, and simpler stereoscopic imaging.贝塞尔光束在活样本中的扩展双光子显微镜:更稳定的焦点,更快的体积扫描,以及更简单的立体成像。
Front Cell Neurosci. 2014 May 20;8:139. doi: 10.3389/fncel.2014.00139. eCollection 2014.
7
Multicolor two-photon light-sheet microscopy.多色双光子光片显微镜术
Nat Methods. 2014 Jun;11(6):600-1. doi: 10.1038/nmeth.2963.
8
Precisely and accurately localizing single emitters in fluorescence microscopy.精确且准确地定位荧光显微镜中的单个发射器。
Nat Methods. 2014 Mar;11(3):253-66. doi: 10.1038/nmeth.2843.
9
Improving spinning disk confocal microscopy by preventing pinhole cross-talk for intravital imaging.通过防止针孔串扰提高活细胞成像的旋转盘共聚焦显微镜性能。
Proc Natl Acad Sci U S A. 2013 Feb 26;110(9):3399-404. doi: 10.1073/pnas.1216696110. Epub 2013 Feb 11.
10
Fast two-photon in vivo imaging with three-dimensional random-access scanning in large tissue volumes.快速双光子在大组织体积中的三维随机存取扫描的体内成像。
Nat Methods. 2012 Jan 8;9(2):201-8. doi: 10.1038/nmeth.1851.