Hams, Emily, Bermingham, Rachel, Wurlod, Felicity A., Hogan, Andrew E., O'Shea, Donal, Preston, Roger J., Rodewald, Hans-Reimer, McKenzie, Andrew N.J. and Fallon, Padraic G. (2016) The helminth T2 RNase v1 promotes metabolic homeostasis in an IL-33– and group 2 innate lymphoid cell–dependent mechanism. The FASEB Journal, 30. pp. 824-835. ISSN 0892-6638
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Abstract
Induction of a type 2 cellular response in
the white adipose tissue leads to weight loss and improves
glucose homeostasis in obese animals. Injection of obese
mice with recombinant helminth-derived Schistosoma mansoni
egg-derived v1 (v1), a potent inducer of type 2 activation, improves metabolic status involving a mechanism
reliant upon release of the type 2 initiator cytokine IL-33.
IL-33 initiates the accumulation of group 2 innate lymphoid cells (ILC2s), eosinophils, and alternatively activated macrophages in the adipose tissue. IL-33 release
from cells in the adipose tissue is mediated by the RNase
activity of v1; however, the ability of v1 to improve metabolic status is reliant upon effective binding of v1 to
CD206. We demonstrate a novel mechanism for RNasemediated release of IL-33 inducing ILC2-dependent improvements in the metabolic status of obese animals.—
Hams, E., Bermingham, R., Wurlod, F. A., Hogan, A. E.,
O’Shea, D., Preston, R. J., Rodewald, H.-R., McKenzie,
A. N. J., Fallon, P. G. The helminth T2 RNase v1 promotes metabolic homeostasis in an IL-33– and group 2
innate lymphoid cell–dependent mechanism.
Item Type: | Article |
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Keywords: | obesity; adipocytes; inflammation; |
Academic Unit: | Faculty of Science and Engineering > Biology |
Item ID: | 12402 |
Identification Number: | 10.1096/fj.15-277822 |
Depositing User: | Andrew Hogan |
Date Deposited: | 10 Feb 2020 17:44 |
Journal or Publication Title: | The FASEB Journal |
Publisher: | Federation of American Society of Experimental Biology |
Refereed: | Yes |
Related URLs: | |
URI: | https://mural.maynoothuniversity.ie/id/eprint/12402 |
Use Licence: | This item is available under a Creative Commons Attribution Non Commercial Share Alike Licence (CC BY-NC-SA). Details of this licence are available here |
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