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Fibroblastic reticular cells in lymph node potentiate white adipose tissue beiging through neuro-immune crosstalk in male mice

Lymph nodes (LNs) are always embedded in the metabolically-active white adipose tissue (WAT), whereas their functional relationship remains obscure. Here, we identify fibroblastic reticular cells (FRCs) in inguinal LNs (iLNs) as a major source of IL-33 in mediating cold-induced beiging and thermogen...

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Autores principales: Cheong, Lai Yee, Wang, Baile, Wang, Qin, Jin, Leigang, Kwok, Kelvin H. M., Wu, Xiaoping, Shu, Lingling, Lin, Huige, Chung, Sookja Kim, Cheng, Kenneth K. Y., Hoo, Ruby L. C., Xu, Aimin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9984541/
https://www.ncbi.nlm.nih.gov/pubmed/36869026
http://dx.doi.org/10.1038/s41467-023-36737-0
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author Cheong, Lai Yee
Wang, Baile
Wang, Qin
Jin, Leigang
Kwok, Kelvin H. M.
Wu, Xiaoping
Shu, Lingling
Lin, Huige
Chung, Sookja Kim
Cheng, Kenneth K. Y.
Hoo, Ruby L. C.
Xu, Aimin
author_facet Cheong, Lai Yee
Wang, Baile
Wang, Qin
Jin, Leigang
Kwok, Kelvin H. M.
Wu, Xiaoping
Shu, Lingling
Lin, Huige
Chung, Sookja Kim
Cheng, Kenneth K. Y.
Hoo, Ruby L. C.
Xu, Aimin
author_sort Cheong, Lai Yee
collection PubMed
description Lymph nodes (LNs) are always embedded in the metabolically-active white adipose tissue (WAT), whereas their functional relationship remains obscure. Here, we identify fibroblastic reticular cells (FRCs) in inguinal LNs (iLNs) as a major source of IL-33 in mediating cold-induced beiging and thermogenesis of subcutaneous WAT (scWAT). Depletion of iLNs in male mice results in defective cold-induced beiging of scWAT. Mechanistically, cold-enhanced sympathetic outflow to iLNs activates β1- and β2-adrenergic receptor (AR) signaling in FRCs to facilitate IL-33 release into iLN-surrounding scWAT, where IL-33 activates type 2 immune response to potentiate biogenesis of beige adipocytes. Cold-induced beiging of scWAT is abrogated by selective ablation of IL-33 or β1- and β2-AR in FRCs, or sympathetic denervation of iLNs, whereas replenishment of IL-33 reverses the impaired cold-induced beiging in iLN-deficient mice. Taken together, our study uncovers an unexpected role of FRCs in iLNs in mediating neuro-immune interaction to maintain energy homeostasis.
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spelling pubmed-99845412023-03-05 Fibroblastic reticular cells in lymph node potentiate white adipose tissue beiging through neuro-immune crosstalk in male mice Cheong, Lai Yee Wang, Baile Wang, Qin Jin, Leigang Kwok, Kelvin H. M. Wu, Xiaoping Shu, Lingling Lin, Huige Chung, Sookja Kim Cheng, Kenneth K. Y. Hoo, Ruby L. C. Xu, Aimin Nat Commun Article Lymph nodes (LNs) are always embedded in the metabolically-active white adipose tissue (WAT), whereas their functional relationship remains obscure. Here, we identify fibroblastic reticular cells (FRCs) in inguinal LNs (iLNs) as a major source of IL-33 in mediating cold-induced beiging and thermogenesis of subcutaneous WAT (scWAT). Depletion of iLNs in male mice results in defective cold-induced beiging of scWAT. Mechanistically, cold-enhanced sympathetic outflow to iLNs activates β1- and β2-adrenergic receptor (AR) signaling in FRCs to facilitate IL-33 release into iLN-surrounding scWAT, where IL-33 activates type 2 immune response to potentiate biogenesis of beige adipocytes. Cold-induced beiging of scWAT is abrogated by selective ablation of IL-33 or β1- and β2-AR in FRCs, or sympathetic denervation of iLNs, whereas replenishment of IL-33 reverses the impaired cold-induced beiging in iLN-deficient mice. Taken together, our study uncovers an unexpected role of FRCs in iLNs in mediating neuro-immune interaction to maintain energy homeostasis. Nature Publishing Group UK 2023-03-03 /pmc/articles/PMC9984541/ /pubmed/36869026 http://dx.doi.org/10.1038/s41467-023-36737-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Cheong, Lai Yee
Wang, Baile
Wang, Qin
Jin, Leigang
Kwok, Kelvin H. M.
Wu, Xiaoping
Shu, Lingling
Lin, Huige
Chung, Sookja Kim
Cheng, Kenneth K. Y.
Hoo, Ruby L. C.
Xu, Aimin
Fibroblastic reticular cells in lymph node potentiate white adipose tissue beiging through neuro-immune crosstalk in male mice
title Fibroblastic reticular cells in lymph node potentiate white adipose tissue beiging through neuro-immune crosstalk in male mice
title_full Fibroblastic reticular cells in lymph node potentiate white adipose tissue beiging through neuro-immune crosstalk in male mice
title_fullStr Fibroblastic reticular cells in lymph node potentiate white adipose tissue beiging through neuro-immune crosstalk in male mice
title_full_unstemmed Fibroblastic reticular cells in lymph node potentiate white adipose tissue beiging through neuro-immune crosstalk in male mice
title_short Fibroblastic reticular cells in lymph node potentiate white adipose tissue beiging through neuro-immune crosstalk in male mice
title_sort fibroblastic reticular cells in lymph node potentiate white adipose tissue beiging through neuro-immune crosstalk in male mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9984541/
https://www.ncbi.nlm.nih.gov/pubmed/36869026
http://dx.doi.org/10.1038/s41467-023-36737-0
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