Whole-tissue 3D imaging reveals intra-adipose sympathetic plasticity regulated by NGF-TrkA signal in cold-induced beiging

Abstract Sympathetic arborizations act as the essential efferent signals in regulating the metabolism of peripheral organs including white adipose tissues (WAT). However, whether these local neural structures would be of plastic nature, and how such plasticity might participate in specific metabolic...

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Main Authors: Ying Cao, Huanhuan Wang, Wenwen Zeng
Format: Article
Language:English
Published: SpringerOpen 2018-03-01
Series:Protein & Cell
Subjects:
NGF
Online Access:http://link.springer.com/article/10.1007/s13238-018-0528-5
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spelling doaj-af1979e35c864550a91388405942726f2020-11-25T00:36:28ZengSpringerOpenProtein & Cell1674-800X1674-80182018-03-019652753910.1007/s13238-018-0528-5Whole-tissue 3D imaging reveals intra-adipose sympathetic plasticity regulated by NGF-TrkA signal in cold-induced beigingYing Cao0Huanhuan Wang1Wenwen Zeng2Center for Life Sciences, Tsinghua UniversitySchool of Life Sciences, Peking UniversityCenter for Life Sciences, Tsinghua UniversityAbstract Sympathetic arborizations act as the essential efferent signals in regulating the metabolism of peripheral organs including white adipose tissues (WAT). However, whether these local neural structures would be of plastic nature, and how such plasticity might participate in specific metabolic events of WAT, remains largely uncharacterized. In this study, we exploit the new volume fluorescence-imaging technique to observe the significant, and also reversible, plasticity of intra-adipose sympathetic arborizations in mouse inguinal WAT in response to cold challenge. We demonstrate that this sympathetic plasticity depends on the cold-elicited signal of nerve growth factor (NGF) and TrkA receptor. Blockage of NGF or TrkA signaling suppresses intra-adipose sympathetic plasticity, and moreover, the cold-induced beiging process of WAT. Furthermore, we show that NGF expression in WAT depends on the catecholamine signal in cold challenge. We therefore reveal the key physiological relevance, together with the regulatory mechanism, of intra-adipose sympathetic plasticity in the WAT metabolism.http://link.springer.com/article/10.1007/s13238-018-0528-5sympathetic plasticityNGFTrkA receptorcold-induced beigingwhole-tissue 3D imaging
collection DOAJ
language English
format Article
sources DOAJ
author Ying Cao
Huanhuan Wang
Wenwen Zeng
spellingShingle Ying Cao
Huanhuan Wang
Wenwen Zeng
Whole-tissue 3D imaging reveals intra-adipose sympathetic plasticity regulated by NGF-TrkA signal in cold-induced beiging
Protein & Cell
sympathetic plasticity
NGF
TrkA receptor
cold-induced beiging
whole-tissue 3D imaging
author_facet Ying Cao
Huanhuan Wang
Wenwen Zeng
author_sort Ying Cao
title Whole-tissue 3D imaging reveals intra-adipose sympathetic plasticity regulated by NGF-TrkA signal in cold-induced beiging
title_short Whole-tissue 3D imaging reveals intra-adipose sympathetic plasticity regulated by NGF-TrkA signal in cold-induced beiging
title_full Whole-tissue 3D imaging reveals intra-adipose sympathetic plasticity regulated by NGF-TrkA signal in cold-induced beiging
title_fullStr Whole-tissue 3D imaging reveals intra-adipose sympathetic plasticity regulated by NGF-TrkA signal in cold-induced beiging
title_full_unstemmed Whole-tissue 3D imaging reveals intra-adipose sympathetic plasticity regulated by NGF-TrkA signal in cold-induced beiging
title_sort whole-tissue 3d imaging reveals intra-adipose sympathetic plasticity regulated by ngf-trka signal in cold-induced beiging
publisher SpringerOpen
series Protein & Cell
issn 1674-800X
1674-8018
publishDate 2018-03-01
description Abstract Sympathetic arborizations act as the essential efferent signals in regulating the metabolism of peripheral organs including white adipose tissues (WAT). However, whether these local neural structures would be of plastic nature, and how such plasticity might participate in specific metabolic events of WAT, remains largely uncharacterized. In this study, we exploit the new volume fluorescence-imaging technique to observe the significant, and also reversible, plasticity of intra-adipose sympathetic arborizations in mouse inguinal WAT in response to cold challenge. We demonstrate that this sympathetic plasticity depends on the cold-elicited signal of nerve growth factor (NGF) and TrkA receptor. Blockage of NGF or TrkA signaling suppresses intra-adipose sympathetic plasticity, and moreover, the cold-induced beiging process of WAT. Furthermore, we show that NGF expression in WAT depends on the catecholamine signal in cold challenge. We therefore reveal the key physiological relevance, together with the regulatory mechanism, of intra-adipose sympathetic plasticity in the WAT metabolism.
topic sympathetic plasticity
NGF
TrkA receptor
cold-induced beiging
whole-tissue 3D imaging
url http://link.springer.com/article/10.1007/s13238-018-0528-5
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AT huanhuanwang wholetissue3dimagingrevealsintraadiposesympatheticplasticityregulatedbyngftrkasignalincoldinducedbeiging
AT wenwenzeng wholetissue3dimagingrevealsintraadiposesympatheticplasticityregulatedbyngftrkasignalincoldinducedbeiging
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