Differences in pulmonary group 2 innate lymphoid cells are dependent on mouse age, sex and strain

Differences in pulmonary group 2 innate lymphoid cells are dependent on mouse age, sex and strain.

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Item Type: Article
Status: Published
Official URL: https://doi.org/10.1111/imcb.12430
Journal or Publication Title: Immunology & Cell Biology
Volume: 99
Number: 5
Page Range: pp. 542-551
Date: 2021
Divisions: UTS Centre for Inflammation
Depositing User: General Admin
Identification Number: 10.1111/imcb.12430
ISSN: 0818-9641
Date Deposited: 10 Jun 2021 06:41
Abstract:

Innate lymphoid cells (ILCs) are resident in the lung and are involved in both the maintenance of homeostasis and the pathogenesis of respiratory diseases. In this study, murine lung ILCs were characterized using flow cytometry and the impact of mouse age, sex and strain were assessed. Lung ILCs were found as early as postnatal day 4 and numbers peaked at 2 weeks, and then decreased as the lung matured. During postnatal lung development, ILC expressed differential amounts of group 2 ILC (ILC2)-associated cell surface antigens including ST2, CD90.2 and ICOS. Using Il5venus Il13td-tomato dual reporter mice, neonates were found to have increased constitutive interleukin (IL)-13 expression compared with adult mice. Neonates and adults had similar ratios of IL-5+ CD45+ leukocytes; however, these cells were mostly composed of ILCs in neonates and T cells in adults. Sex-specific differences in ILC numbers were also observed, with females having greater numbers of lung ILCs than males in both neonatal and adult mice. Female lung ILCs also expressed higher levels of ICOS and decreased KLRG1. Mouse strain also impacted on lung ILCs with BALB/c mice having more ILCs in the lung and increased expression of ST2 and ICOS compared with C57BL/6J mice. Collectively, these data show that lung ILC numbers, cell surface antigen expression, IL-5 and IL-13 levels differed between neonatal and adult lung ILCs. In addition, cell surface antigens commonly used for ILC2 quantification, such as ST2, CD90.2 and ICOS, differ depending on age, sex and strain and these are important considerations for consistent universal identification of lung ILC2s.

© 2021 Australian and New Zealand Society for Immunology, Inc.

Creators:
Creators
Email
Loering, Svenja
UNSPECIFIED
Cameron, Guy JM
UNSPECIFIED
Bhatt, Nirmal P
UNSPECIFIED
Belz, Gabrielle T
UNSPECIFIED
Foster, Paul S
UNSPECIFIED
Hansbro, Philip M
UNSPECIFIED
Starkey, Malcolm R
UNSPECIFIED
Last Modified: 10 Jun 2021 06:41
URI: https://eprints.centenary.org.au/id/eprint/1044

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