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Live Cell Imaging

Leica Microsystems provides you with intelligent innovations in live-cell imaging. Our solutions help you get the best image quality while protecting your samples.

With the variety of fluorescent proteins and multicolored probes that have been developed, it is now possible to label virtually any molecule. The ability to visualize protein dynamics in vesicles, organelles, cells, and tissues has provided new insights into how cells function in healthy and disease states. These insights include the spatiotemporal dynamics of processes like mitosis, embryonic development, and cytoskeleton changes. When studying live cells, common obstacles include phototoxicity and photodamage. To capture fast biological processes, it is crucial to keep the cells healthy and obtain crisp images for reliable data that are free of artifacts. Live‐cell microscopy often requires a compromise between image quality and cell health. During imaging, certain environmental conditions must be maintained to avoid changes in the cells. 

A variety of high-performance Leica live cell imaging solutions can overcome these challenges for live-cell imaging enabling new information for cellular physiology and dynamics to be discovered. 

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Our experts on solutions for live cell imaging applications are happy to help you with their advice.

Your Live Cell Imaging Needs

To perform successful live-cell imaging experiments, using the right platform is critical. When choosing an optical microscope for live‐cell imaging, the following 3 variables should be considered: detector sensitivity (signal‐to‐noise ratio), specimen viability, and image-acquisition speed.

Methods suitable for live-cell applications enable visualization of the dynamics without causing cell damage, as it can affect the results.

Leica Microsystems offers the latest innovations in widefield and confocal imaging technologies for fast 3D live cell imaging with the THUNDER Imagers, Mica – the world’s first Microhub, STELLARIS confocal platform, and FLIM.

Live‐cell imaging is mainly performed with fluorescence microscopy. Widefield microscopy, providing flexible excitation and fast acquisition, is typically used to visualize cell dynamics and development over long times. Confocal microscopy is typically used to study subcellular dynamic events. Multiphoton microscopy allows excitation with longer wavelength light reducing photobleaching and extending cell viability. Finally, fluorescence lifetime imaging (FLIM) can be applied to study fast dynamic signaling events in cells.

Live Cell Imaging System DMi8

The modular DMi8 inverted microscope is the heart of the DMi8 S platform solution. For routine to live cell research, the DMi8 S platform is a complete solution. Whether you need to precisely follow the development of a single cell in a dish, screen through multiple assays, obtain single molecule resolution, or tease out behaviors of complex processes, a DMi8 S system will enable you to see more, see faster, and find the hidden.

Cell Viability & Dynamics During Live Cell Imaging

Leica Microsystems provides you with intelligent innovations in live-cell imaging. Our solutions help you get the best image quality while protecting your samples. Most cellular processes occur in 3 dimensions over time. Therefore, cells need to be imaged in four dimensions (XYZ and time) to obtain a complete picture. Time‐lapse imaging is used to capture cell events over timescales from seconds to months. Repeated imaging of cells at particular points in time is also possible. To protect cell viability during this process, live-cell imaging requires the temperature, pH, and humidity to be kept under control. Light exposure should also be at a minimum to avoid phototoxicity.

Leica Microsystems offers imaging solutions that help optimize your study of live cells, even over long periods of time. They provide the necessary image contrast and resolution to facilitate the analysis of dynamic events. Some Leica systems also enable high-speed imaging and absolute correlated labels without spatiotemporal mismatch between labels of the same time point, so no key cellular events are missed.

Live cell imaging with STELLARIS confocal platform

The STELLARIS platform provides you with solutions whether you need long acquisition times for high-resolution 3D reconstructions or the highest frame rates to capture rapid dynamic events.

STELLARIS is a completely re-imagined confocal microscope platform. STELLARIS confocal microscopes can be combined with all Leica modalities, including FLIM, STED, DLS, and CRS. With the STELLARIS confocal platform, we have re-imagined confocal microscopy to get you closer to the truth.

About Live Cell Imaging

Besides the structural organization of cells or organs, dynamic processes are a major contributor to a functioning biological entity. Naturally, these processes can be best observed in living cells with non-invasive techniques like optical methods, collectively called “live-cell imaging” methods. Live-cell imaging covers all techniques where live cells are observed with microscopes – from the observation of embryogenesis with stereo microscopes, via cell growth studies with compound microscopes, until studies of physiological states of cells or cellular transport using fluorescent dyes or proteins. Although being highly demanding for both, experimenter and equipment (e.g. imaging systems, climate control), live-cell imaging techniques deliver results that are indispensable for present-day research.

This confocal image shows one scan layer of the acoel worm Isodiametra pulchra. The following parts are stained: cyan: nuclei, green: stem cells, magenta: expression of the genes T-Brain/Eomes (gonads und oocytes). Left: anterior. The worm is about 1 mm of size. Photo: Aina Børve, Sars

Download The Guide to Live Cell Imaging

In life science research, live cell imaging is an indispensable tool to visualize cells in a state as in vivo as possible.

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Live cell imaging related articles

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The knowledge portal of Leica Microsystems offers scientific research and teaching material on the subjects of microscopy. The content is designed to support beginners, experienced practitioners and scientists alike in their everyday work and experiments.

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Developing embryos of different species at different stages during the elongation of their posterior body axis, from left to right in developmental time. The labelled regions in red depict a region of undifferentiated cells called the tailbud, with the corresponding region generated from that tissue shaded in grey. Upper row: lamprey; middle row: catshark; bottom row, zebrafish. This figure has been adapted from the following publication: Steventon, B., Duarte, F., Lagadec, R., Mazan, S., Nicolas, J.-F., & Hirsinger, E. (2016). Species tailoured contribution of volumetric growth and tissue convergence to posterior body elongation in vertebrates. Development, 2016. 143(10):1732-41

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