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Multiphoton intravital microscopy of rodents.

Colinda L G J Scheele ,
David Herrmann ,
Erika Yamashita ,
Cristina Lo Celso ,
Craig N Jenne ,
Maja H Oktay ,
David Entenberg ,
Peter Friedl ,
Roberto Weigert ,
Franck L B Meijboom ,
Masaru Ishii ,
Paul Timpson ,
Jacco van Rheenen

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.

More about this publication

Nature reviews. Methods primers

Volume 2
Publication date 01-01-2022

Full text links

Publisher website (DOI) 10.1038/s43586-022-00168-w
Europe PubMed Central 37621948
Pubmed 37621948

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