Multiphoton intravital microscopy of rodents

Publication date

2022-11-10

Authors

Scheele, Colinda L.G.J.
Herrmann, David
Yamashita, Erika
Lo Celso, Cristina
Jenne, Craig N.
Oktay, Maja H.
Entenberg, David
Friedl, Peter
Weigert, Roberto
Meijboom, F.L.B.ORCID 0000-0002-0752-016XISNI 0000000391535379

Editors

Advisors

Supervisors

Document Type

Article
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License

taverne

Abstract

Tissues are heterogeneous with respect to cellular and non-cellular components and in the dynamic interactions between these elements. To study the behaviour and fate of individual cells in these complex tissues, intravital microscopy (IVM) techniques such as multiphoton microscopy have been developed to visualize intact and live tissues at cellular and subcellular resolution. IVM experiments have revealed unique insights into the dynamic interplay between different cell types and their local environment, and how this drives morphogenesis and homeostasis of tissues, inflammation and immune responses, and the development of various diseases. This Primer introduces researchers to IVM technologies, with a focus on multiphoton microscopy of rodents, and discusses challenges, solutions and practical tips on how to perform IVM. To illustrate the unique potential of IVM, several examples of results are highlighted. Finally, we discuss data reproducibility and how to handle big imaging data sets.

Keywords

Hematopoietic stem-cells, Neutrophil extracellular traps, Disseminated tumor-cells, Time imaging reveals, Dynamics in-vivo, Bone-marrow, Real-time, Fluorescence recovery, 2-photon excitation, Lymph-nodes, Taverne, General Medicine, General Biochemistry,Genetics and Molecular Biology

Citation

Scheele, C L G J, Herrmann, D, Yamashita, E, Lo Celso, C, Jenne, C N, Oktay, M H, Entenberg, D, Friedl, P, Weigert, R, Meijboom, F L B, Ishii, M, Timpson, P & van Rheenen, J 2022, 'Multiphoton intravital microscopy of rodents', Nature Reviews Methods Primers, vol. 2, no. 1, 89. https://doi.org/10.1038/s43586-022-00168-w