Challenges and limitations for live cell imaging in extreme cold

Many ecosystems thrive in near-0 °C conditions, and the mechanisms supporting life in these conditions remain understudied due to the challenges in reproducing such environments in laboratory conditions. One such example is polar organisms, that have adapted their entire lifecycle to operate below freezing temperatures through largely unknown cellular adaptations. As rapid polar warming threatens these species, elucidating their survival strategies is increasingly urgent. Fluorescence-based optical microscopy has been central to the understanding of the dynamic processes sustaining life at the cellular level, yet most imaging approaches have been developed and validated for conditions near mammalian physiological temperatures. Imaging at low temperature introduces a distinct physical regime in which molecular motion, membrane organisation, protein conformational dynamics, and fluorophore photophysics are fundamentally altered. As a result, imaging tools, fluorescent probes, and super-resolution methods optimised at 37 °C often fail when applied near 0 °C, or they report biased information. Here, we examine the conceptual, technical, and practical challenges associated with live-cell fluorescence microscopy at cold temperatures. We discuss when and why common imaging modalities and labelling strategies break down, and how probe behaviour becomes tightly coupled to local changes in physicochemical environment. We offer a perspective on new biological questions that become accessible for study with a microscopy platform optimised for imaging in cold conditions. We highlight trade-offs in current temperature-control strategies and identify unmet needs in fluorophore design, instrument engineering, and quantitative standards. By framing cold microscopy as a distinct operational regime rather than an extension of conventional live-cell imaging, this Perspective aims to guide the development of robust tools for studying biological systems near-0 °C conditions.

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Publication Details

Journal
Methods and Applications in Fluorescence
Published
2026-07-16
DOI
https://doi.org/10.1088/2050-6120/ae8c12
Primary Topic
Advanced Fluorescence Microscopy Techniques
Type
article
Field-Weighted Citation Impact
0.00

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article

Challenges and limitations for live cell imaging in extreme cold

Clemens F. Kaminski, Francesca W. van Tartwijk, Lloyd S. Peck, Melody Susan Clark et al.
Methods and Applications in Fluorescence
Advanced Fluorescence Microscopy Techniques
article

Challenges and limitations for live cell imaging in extreme cold

Clemens F. Kaminski, Francesca W. van Tartwijk, Lloyd S. Peck, Melody Susan Clark, Amir Rahmani, Anne-Pia Myriam Marty
article en

Abstract

Many ecosystems thrive in near-0 °C conditions, and the mechanisms supporting life in these conditions remain understudied due to the challenges in reproducing such environments in laboratory conditions. One such example is polar organisms, that have adapted their entire lifecycle to operate below freezing temperatures through largely unknown cellular adaptations. As rapid polar warming threatens these species, elucidating their survival strategies is increasingly urgent. Fluorescence-based optical microscopy has been central to the understanding of the dynamic processes sustaining life at the cellular level, yet most imaging approaches have been developed and validated for conditions near mammalian physiological temperatures. Imaging at low temperature introduces a distinct physical regime in which molecular motion, membrane organisation, protein conformational dynamics, and fluorophore photophysics are fundamentally altered. As a result, imaging tools, fluorescent probes, and super-resolution methods optimised at 37 °C often fail when applied near 0 °C, or they report biased information. Here, we examine the conceptual, technical, and practical challenges associated with live-cell fluorescence microscopy at cold temperatures. We discuss when and why common imaging modalities and labelling strategies break down, and how probe behaviour becomes tightly coupled to local changes in physicochemical environment. We offer a perspective on new biological questions that become accessible for study with a microscopy platform optimised for imaging in cold conditions. We highlight trade-offs in current temperature-control strategies and identify unmet needs in fluorophore design, instrument engineering, and quantitative standards. By framing cold microscopy as a distinct operational regime rather than an extension of conventional live-cell imaging, this Perspective aims to guide the development of robust tools for studying biological systems near-0 °C conditions.

Methods and Applications in Fluorescence
British Antarctic Survey (GB), University of Cambridge (GB)
Wellcome Trust, UK Research and Innovation, Medical Research Council, Engineering and Physical Sciences Research Council, Natural Environment Research Council, British Antarctic Survey
Life in Land
Openalex Percentile: Top 9%
Advanced Fluorescence Microscopy Techniques
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