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Optical toolkits for in vivo deep tissue laser scanning microscopy: a primer

Lee, Woei Ming (Steve); McMenamin, Thomas; Li, Yongxiao

Description

Life at the microscale is animated and multifaceted. The impact of dynamic in vivo microscopy in small animals has opened up opportunities to peer into a multitude of biological processes at the cellular scale in their native microenvironments. Laser scanning microscopy (LSM) coupled with targeted fluorescent proteins has become an indispensable tool to enable dynamic imaging in vivo at high temporal and spatial resolutions. In the last few decades, the technique has been translated from...[Show more]

dc.contributor.authorLee, Woei Ming (Steve)
dc.contributor.authorMcMenamin, Thomas
dc.contributor.authorLi, Yongxiao
dc.date.accessioned2019-04-10T11:08:25Z
dc.identifier.issn0150-536X
dc.identifier.urihttp://hdl.handle.net/1885/159451
dc.description.abstractLife at the microscale is animated and multifaceted. The impact of dynamic in vivo microscopy in small animals has opened up opportunities to peer into a multitude of biological processes at the cellular scale in their native microenvironments. Laser scanning microscopy (LSM) coupled with targeted fluorescent proteins has become an indispensable tool to enable dynamic imaging in vivo at high temporal and spatial resolutions. In the last few decades, the technique has been translated from imaging cells in thin samples to mapping cells in the thick biological tissue of living organisms. Here, we sought to provide a concise overview of the design considerations of a LSM that enables cellular and subcellular imaging in deep tissue. Individual components under review include: long working distance microscope objectives, laser scanning technologies, adaptive optics devices, beam shaping technologies and photon detectors, with an emphasis on more recent advances. The review will conclude with the latest innovations in automated optical microscopy, which would impact tracking and quantification of heterogeneous populations of cells in vivo.
dc.format.mimetypeapplication/pdf
dc.language.isoen_AU
dc.publisherInstitute of Physics Publishing
dc.sourceJournal of Optics
dc.titleOptical toolkits for in vivo deep tissue laser scanning microscopy: a primer
dc.typeJournal article
local.description.notesImported from ARIES
local.identifier.citationvolume20
dc.date.issued2018
local.identifier.absfor090606 - Photonics and Electro-Optical Engineering (excl. Communications)
local.identifier.absfor060106 - Cellular Interactions (incl. Adhesion, Matrix, Cell Wall)
local.identifier.ariespublicationu1029610xPUB127
local.type.statusPublished Version
local.contributor.affiliationLee, Woei Ming (Steve), College of Engineering and Computer Science, ANU
local.contributor.affiliationMcMenamin, Thomas, College of Engineering and Computer Science, ANU
local.contributor.affiliationLi, Yongxiao, College of Engineering and Computer Science, ANU
local.description.embargo2039-12-31
local.bibliographicCitation.issue6
local.identifier.doi10.1088/2040-8986/aac4af2040-8978/
local.identifier.absseo861500 - INSTRUMENTATION
dc.date.updated2019-03-12T07:23:48Z
local.identifier.scopusID2-s2.0-85047857495
dc.provenanceJournal: Journal of Optics (ISSN: 2040-8978, ESSN: 2040-8986) [Formerly known as Journal of Optics A: Pure and Applied Optics] RoMEO: This is a RoMEO green journal Paid OA: A paid open access option is available for this journal. Author's Pre-print: green tick author can archive pre-print (ie pre-refereeing) Author's Post-print: green tick author can archive post-print (ie final draft post-refereeing) Publisher's Version/PDF: cross author cannot archive publisher's version/PDF
CollectionsANU Research Publications

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