Abstract

BackgroundThe transmitted light detectors present on most modern confocal microscopes are an under-utilised tool for the live imaging of plant cells. As the light forming the image in this detector is not passed through a pinhole, out-of-focus light is not removed. It is this extended focus that allows the transmitted light image to provide cellular and organismal context for fluorescence optical sections generated confocally. More importantly, the transmitted light detector provides images that have spatial and temporal registration with the fluorescence images, unlike images taken with a separately-mounted camera.ResultsBecause plants often provide difficulties for taking transmitted light images, with the presence of pigments and air pockets in leaves, this study documents several approaches to improving transmitted light images beginning with ensuring that the light paths through the microscope are correctly aligned (Köhler illumination). Pigmented samples can be imaged in real colour using sequential scanning with red, green and blue lasers. The resulting transmitted light images can be optimised and merged in ImageJ to generate colour images that maintain registration with concurrent fluorescence images. For faster imaging of pigmented samples, transmitted light images can be formed with non-absorbed wavelengths. Transmitted light images of Arabidopsis leaves expressing GFP can be improved by concurrent illumination with green and blue light. If the blue light used for YFP excitation is blocked from the transmitted light detector with a cheap, coloured glass filters, the non-absorbed green light will form an improved transmitted light image. Changes in sample colour can be quantified by transmitted light imaging. This has been documented in red onion epidermal cells where changes in vacuolar pH triggered by the weak base methylamine result in measurable colour changes in the vacuolar anthocyanin.ConclusionsMany plant cells contain visible levels of pigment. The transmitted light detector provides a useful tool for documenting and measuring changes in these pigments while maintaining registration with confocal imaging.

Highlights

  • The transmitted light detectors present on most modern confocal microscopes are an under-utilised tool for the live imaging of plant cells

  • Recent decades have seen a revolution in the imaging of living plant cells, with the expression of green fluorescent protein targeted to almost all locations within the plant cell [1] through different protocols including transient particle bombardment [2,3,4], virus-mediated infection [5, 6] and stable Agrobacterium-based transformations

  • As a consequence of this, these transmitted light detector images can be combined with the fluorescence images into overlays in ways not possible with photographs taken with an external camera [16]

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Summary

Introduction

The transmitted light detectors present on most modern confocal microscopes are an under-utilised tool for the live imaging of plant cells. GFP expression has been visualised with advances in microscopy including the advent on confocal and two photon microscopy [8,9,10] and the more recent arrival of super-resolution imaging [11,12,13] and light sheet microscopy [14, 15]. These fluorescence techniques typically use microscopes in the epifluorescence configuration in which the excitation and emission light is delivered and collected through the same lens. As a consequence of this, these transmitted light detector images can be combined with the fluorescence images into overlays in ways not possible with photographs taken with an external camera [16]

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