Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/38641
Title: Viewing immune regulation as it happens: In vivo imaging for investigation of regulatory T-cell function.
Authors: Hickey M.J.;Chow Z.
Institution: (Hickey, Chow) Centre for Inflammatory Diseases, Department of Medicine, Monash University, Monash Medical Centre, 246 Clayton Road, Clayton, VIC 3168, Australia
Issue Date: 9-Jul-2017
Copyright year: 2017
Publisher: Nature Publishing Group (Houndmills, Basingstoke, Hampshire RG21 6XS, United Kingdom)
Place of publication: United Kingdom
Publication information: Immunology and Cell Biology. 95 (6) (pp 514-519), 2017. Date of Publication: 01 Jul 2017.
Journal: Immunology and Cell Biology
Abstract: Regulatory T cells (Tregs) play indispensable roles in the immune system, in limiting excessive or inappropriate immune and inflammatory responses. They achieve this function via effects on other immune cells in the secondary lymphoid system, and in peripheral locations such as skin, gut and bone marrow. As for the more extensively studied cellular players in the immune system, particularly dendritic cells and conventional T cells, in vivo imaging of Tregs via two-photon (or multiphoton) microscopy (MPM) has been central to the development of understanding how these cells function. In this brief review, we will describe the studies that have utilised MPM to examine Treg behaviour in vivo. These studies have investigated Treg behaviour in lymph nodes and spleen, as well as in peripheral organs such as skin, small intestine and bone marrow. The findings from these experiments underline how assumptions made about Treg function based on results of in vitro experiments are often not supported by direct visualisation of these cells in their normal in vivo settings. Together this work reveals that only via MPM analysis can Treg function be investigated in the complicated multicellular environments where conventional T cells, antigen-presenting cells and other potential cellular targets of Tregs are present with each undergoing their own specific actions.Copyright © 2017 Australasian Society for Immunology Inc. All rights reserved.
DOI: http://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1038/icb.2017.33
PubMed URL: 28420873 [http://www.ncbi.nlm.nih.gov/pubmed/?term=28420873]
ISSN: 0818-9641
URI: https://repository.monashhealth.org/monashhealthjspui/handle/1/38641
Type: Review
Appears in Collections:Articles

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