Imaging Flow Cytometry to Assess Antigen-Presenting-Cell Function.


Journal

Current protocols in immunology
ISSN: 1934-368X
Titre abrégé: Curr Protoc Immunol
Pays: United States
ID NLM: 9101651

Informations de publication

Date de publication:
06 2019
Historique:
pubmed: 7 3 2019
medline: 28 3 2020
entrez: 7 3 2019
Statut: ppublish

Résumé

This unit describes methods for quantifying phagocytosis and imaging the immunological synapse between T cells and antigen-presenting cells (APCs), with both techniques delivering valuable information about APC function. These aspects of APC biology have traditionally been challenging to quantify, and imaging flow cytometry, which harnesses the high-throughput nature of flow cytometry combined with the capacity of microscopy to deliver spatial localization, facilitates analysis of these APC functions in a fashion that was previously not possible. Imaging flow cytometry allows large numbers of events to be captured and large amounts of fluorescence data to be quantified at the physical location of markers of interest, both on the cell surface and in intracellular compartments, combining key features of traditional flow cytometry and fluorescence microscopy. © 2019 by John Wiley & Sons, Inc.

Identifiants

pubmed: 30840360
doi: 10.1002/cpim.72
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e72

Informations de copyright

© 2019 John Wiley & Sons, Inc.

Auteurs

Kate A Markey (KA)

Memorial Sloan Kettering Cancer Center, New York, New York.

Kate H Gartlan (KH)

QIMR Berghofer Medical Research Institute, Brisbane, Australia.
Fred Hutchinson Cancer Research Center, Seattle, Washington.

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Classifications MeSH