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Methods Mol Biol. 2019;1930:75-82. doi: 10.1007/978-1-4939-9036-8_10.

Live Imaging of Resident T-Cell Migration in Human Lymphoid Tissue Slices Using Confocal Microscopy.

Author information

1
Département Immunologie, Inflammation, et Infection, INSERM, U1016, Institut Cochin, Paris, France. emmanuel.donnnadieu@inserm.fr.
2
CNRS, UMR8104, Paris, France. emmanuel.donnnadieu@inserm.fr.
3
Université Paris Descartes, Sorbonne Paris Cité, Paris, France. emmanuel.donnnadieu@inserm.fr.
4
Dr. Senckenbergisches Institut für Pathologie, Klinikum der Johann Wolfgang Goethe-Universität, Frankfurt am Main, Germany.
5
Frankfurt Institute for Advanced Studies (FIAS), Frankfurt am Main, Germany.

Abstract

In order to mount a potent immune response, immune cells must move actively through tissues. As an example, T-cell need to migrate within lymph nodes in order to scan the surface of many dendritic cells and recognize rare expressed antigens. The recent development of improved imaging approaches, such as two-photon microscopy, and the use of powerful mouse models have shed light on some of the mechanisms that regulate the migration of immune cells in many organs. Whereas such systems have provided valuable insights, they do not always predict human responses. In human, our knowledge in the field mainly comes from a description of fixed tissue samples. However, these studies lack a temporal dimension since samples have been fixed. In order to overcome some of these limitations, we describe, in this methodology chapter, an experimental system of fresh human adenoid slices to monitor the dynamics of resident T-lymphocytes that have been stained with directly-coupled fluorescent antibodies. Combined with confocal fluorescent imaging, this preparation offers an effective approach to imaging immune cells in a three-dimensional (3D) human lymphoid tissue environment.

KEYWORDS:

Confocal microscopy; Immunostaining; Motility; T-cells; Vibratome

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