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Article: Adiponectin-expressing Treg facilitate T lymphocyte development in thymic nurse cell complexes

TitleAdiponectin-expressing Treg facilitate T lymphocyte development in thymic nurse cell complexes
Authors
Issue Date2021
PublisherNature Research: Fully open access journals. The Journal's web site is located at http://www.nature.com/commsbio
Citation
Communications Biology, 2021, v. 4, p. article no. 344 How to Cite?
AbstractAdiponectin is a well-known insulin sensitizer and anti-inflammatory molecule, possessing therapeutic potentials in cardiovascular, metabolic and cancer diseases. Results of the present study demonstrate that adiponectin is expressed in a population of regulatory T-cells (Treg) resided within the thymic nurse cell (TNC) complexes. Adoptive transfer of adiponectin-expressing Treg precursors effectively attenuated obesity, improved glucose and insulin tolerance, prevented fatty liver injuries in wild-type mice fed a high-fat diet, and significantly inhibited breast cancer development in MMTV-PyVT transgenic mice. Within the TNC complexes, locally produced adiponectin bound to and regulated the expression as well as the distribution of CD100, a transmembrane lymphocyte semaphorin, in turn modulating the lymphoepithelial interactions to facilitate T-cell development and maturation. In summary, adiponectin plays an important role in the selection and development of T lymphocytes within the TNC complexes. Adiponectin-expressing Treg represent a promising candidate for adoptive cell immunotherapy against obesity-related metabolic and cancer diseases.
Persistent Identifierhttp://hdl.handle.net/10722/305853
ISSN
2023 Impact Factor: 5.2
2023 SCImago Journal Rankings: 2.090
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorZhang, Y-
dc.contributor.authorCao, H-
dc.contributor.authorChen, J-
dc.contributor.authorLi, Y-
dc.contributor.authorXu, A-
dc.contributor.authorWang, Y-
dc.date.accessioned2021-10-20T10:15:15Z-
dc.date.available2021-10-20T10:15:15Z-
dc.date.issued2021-
dc.identifier.citationCommunications Biology, 2021, v. 4, p. article no. 344-
dc.identifier.issn2399-3642-
dc.identifier.urihttp://hdl.handle.net/10722/305853-
dc.description.abstractAdiponectin is a well-known insulin sensitizer and anti-inflammatory molecule, possessing therapeutic potentials in cardiovascular, metabolic and cancer diseases. Results of the present study demonstrate that adiponectin is expressed in a population of regulatory T-cells (Treg) resided within the thymic nurse cell (TNC) complexes. Adoptive transfer of adiponectin-expressing Treg precursors effectively attenuated obesity, improved glucose and insulin tolerance, prevented fatty liver injuries in wild-type mice fed a high-fat diet, and significantly inhibited breast cancer development in MMTV-PyVT transgenic mice. Within the TNC complexes, locally produced adiponectin bound to and regulated the expression as well as the distribution of CD100, a transmembrane lymphocyte semaphorin, in turn modulating the lymphoepithelial interactions to facilitate T-cell development and maturation. In summary, adiponectin plays an important role in the selection and development of T lymphocytes within the TNC complexes. Adiponectin-expressing Treg represent a promising candidate for adoptive cell immunotherapy against obesity-related metabolic and cancer diseases.-
dc.languageeng-
dc.publisherNature Research: Fully open access journals. The Journal's web site is located at http://www.nature.com/commsbio-
dc.relation.ispartofCommunications Biology-
dc.rightsCommunications Biology. Copyright © Nature Research: Fully open access journals.-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleAdiponectin-expressing Treg facilitate T lymphocyte development in thymic nurse cell complexes-
dc.typeArticle-
dc.identifier.emailZhang, Y: zywhk@hku.hk-
dc.identifier.emailXu, A: amxu@hkucc.hku.hk-
dc.identifier.emailWang, Y: yuwanghk@hku.hk-
dc.identifier.authorityXu, A=rp00485-
dc.identifier.authorityWang, Y=rp00239-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1038/s42003-021-01877-w-
dc.identifier.pmid33727658-
dc.identifier.pmcidPMC7966800-
dc.identifier.scopuseid_2-s2.0-85102701133-
dc.identifier.hkuros328006-
dc.identifier.volume4-
dc.identifier.spagearticle no. 344-
dc.identifier.epagearticle no. 344-
dc.identifier.isiWOS:000630072200005-
dc.publisher.placeUnited Kingdom-

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