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Learn how to effectively image large and deep cleared samples, from sample preparation to data analysis. Discover essential techniques for successful imaging, clearing methods, labeling tips, and choosing the right microscopy system.
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Tips for imaging cleared samples Pablo Ariel, Ph.D. Microscopy Services Laboratory Department of Pathology and Laboratory Medicine
Assumptions: • BIG samples (>2mm diameter) • DEEP imaging (>2mm deep)
Workflow Sample preparation Sample mounting Sample imaging Data management Data visualization Chung et al, Nature 2013 Ertürk et al, 2012 Doboszet al, Neoplasia 2014 Renier et al, Cell2016 Data analysis
Before imaging During imaging
Before imaging During imaging
Trim based on your biology • Smaller samples: • stain faster • require less antibody • clear faster • are easier to image
Clearing – don’t reinvent the wheel Use a clearing method that works • For a question similar to yours • Not just in the lab that created it • With minimal equipment and fuss (avoid $$$) Good results with iDISCO+ on: brains, kidneys, liver, heart, embryos, intestine…
Labeling – (far) redder is better AlexaFluor488 Ex 488; Em525/50 AlexaFluor568 Ex 561; Em595/40 AlexaFluor647 Ex 640; Em 680/30 1 mm Autofluorescence Scattering Absorbtion Renier et al, Cell2014
Before imaging During imaging
What level of detail do you need? detail you want
Example: Labeled axons (0.2mm)
Example: Labeled axons (0.2mm) look bigger without high res optics
Problem: 2 objects close together
Problem: 2 objects close together ?
Problem: 2 objects close together ?
Examples of biological questions Subcellular scale Dense labelling High resolution sub-um(ish) • Discerning subcellular details (spines, organelles) • Counting all cells in densely packed tissue • Tracing individual axons in densely labeled samples Cellular scale Sparse labelling Medium resolution um(ish) • Locate cells of interest in large pieces of tissue • Trace neural circuits • Trace sparsely labeled axons • Analysis of vasculature
Different microscopes for different questions Subcellular scale Dense labelling High resolution sub-um(ish) Some laser scanning systems: Slow, potential for high bleaching, even resolution across field of view Cellular scale Sparse labelling Medium resolution um(ish) Some light-sheet systems: Very fast, low bleaching, uneven resolution across field of view
Different microscopes for different questions Subcellular scale Dense labelling High resolution sub-um(ish) Somelaser scanning systems • Need very special objectives • Long working distance • High resolution (high NA) • Large field of view • Matched to RI of clearing solutions • Big (need special stands) • $$$
Objectives for high resolution volumetric imaging RI RI DBE = 1.56
Implementation challenges • Immersion fluid: • $$ • corrosion • evaporation • RI • Custom sample holders: • Keep sample still • Minimize immersion fluid • Allow space for huge objectives
Fundamental constraints of scanning techniques Low Speed (though ribbon scanning is much faster) High Bleaching For cellular and/or sparse labelling: enter light-sheet…
Features of light-sheet microscopy Objective z x • Sample with fluorophores • Laser sheet • Detection orthogonal to sheet
Compared to scanning, light-sheet is Faster Less damaging Modified from Leica Microsystems
Ultramicroscope Objective Sample LavisionBiotec UltraMicroscope II
To optimize, know the key limitations Sheet shape Better Worse Light propagation Radial aberrations
Sheet shape y x z
Sheet shape • Major problem in Z • Bigger problem at low mag Low mag FOV 10X higher mag FOV y x z
Sheet shape • Major problem in Z Options? • Bigger problem at low mag Low mag FOV 10X higher mag FOV y x z
Sheet shape • Major problem in Z • Bigger problem at low mag Trade Z resolution for evenness: lower sheet NA y x z
Sheet shape • Major problem in Z • Bigger problem at low mag Trade Z resolution for evenness: lower sheet NA y x z
Sheet shape • Major problem in Z • Bigger problem at low mag Trade time for evenness: crop + tile y x z
Sheet shape • Major problem in Z • Bigger problem at low mag Trade time for evenness: crop + tile y x z
Sheet shape • Major problem in Z • Bigger problem at low mag Trade time for evenness: crop + tile y x z
Sheet shape • Major problem in Z • Bigger problem at low mag Trade time for evenness: crop + tile y x z
Sheet shape • Major problem in Z • Bigger problem at low mag Trade time for evenness: crop + tile y x z
Sheet shape • Major problem in Z • Bigger problem at low mag Trade time for evenness: crop + tile y x z
Sheet shape • Major problem in Z • Bigger problem at low mag Trade time for evenness: crop + tile y x z
Sheet shape • Major problem in Z • Bigger problem at low mag Trade time for evenness: Dynamic focus y x z
Sheet shape • Major problem in Z • Bigger problem at low mag Trade time for evenness: Dynamic focus y x z
Sheet shape • Major problem in Z • Bigger problem at low mag Trade time for evenness: Dynamic focus y x z