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ILCs interact with multiple cell types within their local environment to integrate a wealth of different signals into coordinated responses that regulate tissue homeostasis as well as immune responses upon challenge. While the development and function of ILCs has been extensively studied, principally using flow cytometry, there is limited understanding of the precise composition of cellular niches within which ILCs reside. While this might be optimally studied using dynamic live imaging approaches, immunofluorescence staining of tissue sections can provide fundamental basic information regarding the nature of these microenvironments. Here, a methodology enabling the identification of murine and human ILC populations in frozen tissue sections using immunofluorescence is described.

Original publication

DOI

10.1007/978-1-0716-0338-3_5

Type

Chapter

Publication Date

01/2020

Volume

2121

Pages

51 - 58

Addresses

Institute of Immunology and Immunotherapy, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK. eed107@alumni.bham.ac.uk.

Keywords

Lymph Nodes, Lymphocytes, Animals, Humans, Mice, Fluorescent Antibody Technique, Flow Cytometry, Interleukin-7 Receptor alpha Subunit, Immunity, Innate, Nuclear Receptor Subfamily 1, Group F, Member 3, CD3 Complex