Cookies

We use cookies to ensure that we give you the best experience on our website. By continuing to browse this repository, you give consent for essential cookies to be used. You can read more about our Privacy and Cookie Policy.


Durham Research Online
You are in:

Multi-plane remote refocussing epifluorescence microscopy to image dynamic Ca2+ events.

Lawton, P.F. and Buckley, C. and Saunter, C.D. and Wilson, C. and Corbett, A.D. and Salter, P.S. and McCarron, J.G. and Girkin, J.M. (2019) 'Multi-plane remote refocussing epifluorescence microscopy to image dynamic Ca2+ events.', Biomedical optics express., 10 (11). pp. 5611-5624.

Abstract

Rapid imaging of multiple focal planes without sample movement may be achieved through remote refocusing, where imaging is carried out in a plane conjugate to the sample plane. The technique is ideally suited to studying the endothelial and smooth muscle cell layers of blood vessels. These are intrinsically linked through rapid communication and must be separately imaged at a sufficiently high frame rate in order to understand this biologically crucial interaction. We have designed and implemented an epifluoresence-based remote refocussing imaging system that can image each layer at up to 20fps using different dyes and excitation light for each layer, without the requirement for optically sectioning microscopy. A novel triggering system is used to activate the appropriate laser and image acquisition at each plane of interest. Using this method, we are able to achieve axial plane separations down to 15 ????m, with a mean lateral stability of ≤ 0.32 ????m displacement using a 60x, 1.4NA imaging objective and a 60x, 0.7NA reimaging objective. The system allows us to image and quantify endothelial cell activity and smooth muscle cell activity at a high framerate with excellent lateral and good axial resolution without requiring complex beam scanning confocal microscopes, delivering a cost effective solution for imaging two planes rapidly. We have successfully imaged and analysed Ca2+ activity of the endothelial cell layer independently of the smooth muscle layer for several minutes.

Item Type:Article
Full text:(VoR) Version of Record
Available under License - Creative Commons Attribution.
Download PDF
(4248Kb)
Status:Peer-reviewed
Publisher Web site:https://doi.org/10.1364/BOE.10.005611
Publisher statement:Published by The Optical Society under the terms of the Creative Commons Attribution 4.0 License. Further distribution of this work must maintain attribution to the author(s) and the published article's title, journal citation, and DOI.
Date accepted:12 September 2019
Date deposited:11 October 2019
Date of first online publication:10 October 2019
Date first made open access:No date available

Save or Share this output

Export:
Export
Look up in GoogleScholar