Discovery Blog

At the Speed of Life—Light Sheet Microscopy Advances for Biological Imaging

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Cleared Zebrafish larvae head vascular and neural staining captured with an Alpha3 light sheet fluorescence microscope

Cleared Zebrafish larvae head vascular and neural staining. Captured at 20x with 0.5 NA. and CUBIC-2. Image courtesy of P. Affaticati & A. Jenett of the Tefor Facility, France.

We live in a three-dimensional ever-changing world. Yet in microscopy, our ability to image in 3D and at the speeds required to observe fast living processes remains a challenge. Compared to other light microscopy techniques, fluorescence microscopy can achieve high specificity and contrast, though there are still major limitations in signal-to-noise ratio and phototoxicity.

Traditional approaches, such as confocal microscopy, eliminate out-of-focus light, a process known as optical sectioning, using a pinhole within the focal plane. Although this method offers an increased signal-to-noise ratio, the sample must still be exposed repeatedly to large amounts of out-of-focus light, increasing the likelihood of photobleaching.

Laser scanning confocal

Laser scanning confocal

Spinning disk confocal

Spinning disk confocal

Light sheet

Light sheet

And Then There Was Light—The Advent of Light Sheet Microscopy

In the early 1900s, scientists began looking for a way to improve biological imaging. One such technology arose in 1902 with an optical device called the “Ultramicroscope,” developed by Richard Zsigmondy and Henry Siedentopf (Heddleston & Chew, 2016; Adams et al., 2016). This early light sheet microscope broke away from the traditional optical architecture by separating the illumination and detection light paths, creating the first orthogonal light sheet microscope.

Almost 100 years later, Voie et al. published the first light sheet fluorescence microscope (LSFM) images, using the orthogonal plane architecture to optically section guinea pig cochlea (Heddleston & Chew, 2016; Adams et al., 2016). More recently, variations of LSFMs have been developed to image bacteria, drosophila, zebrafish, and various other tissues.

Bringing Light Sheet Fluorescence Microscopy to the Masses

Modern LSFM systems, also known as selective plane illumination microscopy (SPIM), employ variations of orthogonal architectures like their predecessors, though they use cylindrical lenses to produce a thin sheet of light for optical sectioning. This thin sheet of light excites only a subregion of the sample within the focal plane of the imaging objective. Combined with a high-speed sCMOS camera for emission collection, LSFM provides greater sampling depths, an improved signal-to-noise ratio, and greater imaging speeds for reduced phototoxicity compared to traditional confocal technologies.

Light sheet fluorescence imaging is now recognized as a key microscopy technique for investigating whole organs or live specimens. However, its development among the scientific community is still hampered by the relatively limited scope and capacity to adapt to current model systems. In recent years, “off-the-shelf” LSFM systems have become more readily available to meet the needs of researchers within the biological fields. Not all systems are built alike though, and it is important to consider how different features meet your needs.

4 Important Considerations When Comparing LSFM Systems

There are several important features to think about when deciding which light sheet fluorescence system is best for you.

  1. First and foremost, sample preparation:
    Unlike in traditional microscopy where large fixed samples are typically sectioned and mounted onto slides, light sheet microscopy samples are imaged intact and, therefore, must be optically cleared, which entails making them transparent. There are many protocols for clearing various tissues, and many clearing solutions are also available commercially. I recommend reading “A beginner’s guide to tissue clearing” by Pablo Ariel (Int J Biochem Cell Biol. 2017 Mar. 84: 35–39) for a review of a few popular methods.
  2. Optical architecture:
    The optical architecture for the illumination and detection path can strongly impact the nature and size of the samples that can be observed, as well as the quality of your image. Striping artifacts, for example, are caused by the emitted light refracting off an opaque structure within the sample. To overcome this issue, a plethora of optical architectures have been designed for image acquisition on live or cleared samples of all sizes. One example of these architectures is multidirectional SPIM (mSPIM), in which multiple illumination paths are aligned to illuminate the sample and overcome striping artifacts. While mSPIM systems may offer optimal performance for specific applications, they all share limitations in terms of flexibility, modularity, and practical use, which should be taken into account when selecting a system best suited for your research.
    SPIM

    SPIM

    mSPIM

    mSPIM

    Comparison of striping artifacts with a selective plane illumination microscope system (SPIM) and a mSPIM system

    (Schwarz, et al. PLoS One, 2015)

  3. Sample flexibility:
    While LSFM is a quickly expanding field with new systems coming to market each year, because of their different designs there is a high level of variation in terms of the types of samples they can accommodate. Some systems can only image smaller samples such as spheroids, whereas others can only image larger tissues. They may also be limited to imaging either fixed or live specimens. Although this type of specificity might be ideal for a single user who focuses on one sample type, the ability to share the equipment with an entire research department or to expand your research is compromised. It is important to consider all the potential sample types that your LSFM system will need to be able to handle. Recently, more flexible LSFM systems have been designed to bridge this gap in sample variation. The Alpha3 light sheet fluorescence microscope, for instance, can accommodate a wide variety of specimens, from single cells through to whole mouse brains, including live organisms.*
  4. Data management:
    Lastly, and potentially most importantly, is data management. It is not unheard of for a single experiment to reach 100s of gigabytes (GBs), even terabytes (TBs) of data. Working with your local IT group to create a plan for your data needs is strongly recommended. Be aware you may need to purchase a separate analysis software package to render and analyze such large data sets.

Related Content

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Olympus Fluorescence Digital Image Gallery


*The Alpha3 system is not available in all regions. Please contact your local Olympus rep for more information.

Associate Product Manager

Dr. Joanna Hawryluk is an Associate Product Manager for Research Imaging at Olympus Corporation of the Americas located in Waltham, Massachusetts. She received her doctorate degree from the University of Connecticut in Storrs, Connecticut within the department of Physiology and Neurobiology. Her studies focused on investigating the mechanisms of modulation by voltage-gated KCNQ channels and HCN channels on brainstem chemoreceptive neurons and their control of expiratory drive. She has been with Olympus since 2017 and is currently responsible for the BXWI and OpenStand line of electrophysiology microscopes and the Alpha3 light sheet microscope.

2019年12月9日
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