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Article: Olfactory ecto-mesenchymal stem cells possess immunoregulatory function and suppress autoimmune arthritis

TitleOlfactory ecto-mesenchymal stem cells possess immunoregulatory function and suppress autoimmune arthritis
Authors
KeywordsCIA
Olfactory ecto-mesenchymal stem cells
Treg cell
Issue Date2016
PublisherNature Publishing Group. The Journal's web site is located at http://www.nature.com/cmi/index.html
Citation
Cellular & Molecular Immunology, 2016, v. 13 n. 3, p. 401-408 How to Cite?
AbstractRecent studies have identified olfactory ecto-mesenchymal stem cells (OE-MSCs) as a new type of resident stem cell in the olfactory lamina propria. However, it remains unclear whether OE-MSCs possess any immunoregulatory functions. In this study, we found that mouse OE-MSCs expressed higher transforming growth factor-beta and interleukin-10 levels than bone marrow-derived MSCs. In culture, OE-MSCs exerted their immunosuppressive capacity via directly suppressing effector T-cell proliferation and increasing regulatory T (Treg) cell expansion. In mice with collagen-induced arthritis, adoptive transfer of OE-MSCs markedly suppressed arthritis onset and disease severity, which was accompanied by increased Treg cells and reduced Th1/Th17 cell responses in vivo. Taken together, our findings identified a novel function of OE-MSCs in regulating T-cell responses, indicating that OE-MSCs may represent a new cell therapy for the treatment of rheumatoid arthritis and other autoimmune diseases.
Persistent Identifierhttp://hdl.handle.net/10722/232155
ISSN
2021 Impact Factor: 22.096
2020 SCImago Journal Rankings: 2.500
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorRui, K-
dc.contributor.authorZhang, Z-
dc.contributor.authorTian, J-
dc.contributor.authorLin, X-
dc.contributor.authorWang, X-
dc.contributor.authorMa, J-
dc.contributor.authorTang, X-
dc.contributor.authorXu, H-
dc.contributor.authorLu, L-
dc.contributor.authorWang, S-
dc.date.accessioned2016-09-20T05:28:06Z-
dc.date.available2016-09-20T05:28:06Z-
dc.date.issued2016-
dc.identifier.citationCellular & Molecular Immunology, 2016, v. 13 n. 3, p. 401-408-
dc.identifier.issn1672-7681-
dc.identifier.urihttp://hdl.handle.net/10722/232155-
dc.description.abstractRecent studies have identified olfactory ecto-mesenchymal stem cells (OE-MSCs) as a new type of resident stem cell in the olfactory lamina propria. However, it remains unclear whether OE-MSCs possess any immunoregulatory functions. In this study, we found that mouse OE-MSCs expressed higher transforming growth factor-beta and interleukin-10 levels than bone marrow-derived MSCs. In culture, OE-MSCs exerted their immunosuppressive capacity via directly suppressing effector T-cell proliferation and increasing regulatory T (Treg) cell expansion. In mice with collagen-induced arthritis, adoptive transfer of OE-MSCs markedly suppressed arthritis onset and disease severity, which was accompanied by increased Treg cells and reduced Th1/Th17 cell responses in vivo. Taken together, our findings identified a novel function of OE-MSCs in regulating T-cell responses, indicating that OE-MSCs may represent a new cell therapy for the treatment of rheumatoid arthritis and other autoimmune diseases.-
dc.languageeng-
dc.publisherNature Publishing Group. The Journal's web site is located at http://www.nature.com/cmi/index.html-
dc.relation.ispartofCellular & Molecular Immunology-
dc.subjectCIA-
dc.subjectOlfactory ecto-mesenchymal stem cells-
dc.subjectTreg cell-
dc.titleOlfactory ecto-mesenchymal stem cells possess immunoregulatory function and suppress autoimmune arthritis-
dc.typeArticle-
dc.identifier.emailLin, X: linxiang@hku.hk-
dc.identifier.emailWang, X: xiaohuiwang@hku.hk-
dc.identifier.emailLu, L: liweilu@hkucc.hku.hk-
dc.identifier.authorityLin, X=rp02623-
dc.identifier.authorityWang, X=rp02664-
dc.identifier.authorityLu, L=rp00477-
dc.description.naturelink_to_OA_fulltext-
dc.identifier.doi10.1038/cmi.2015.82-
dc.identifier.pmid26388237-
dc.identifier.pmcidPMC4856806-
dc.identifier.scopuseid_2-s2.0-84966343988-
dc.identifier.hkuros264668-
dc.identifier.volume13-
dc.identifier.issue3-
dc.identifier.spage401-
dc.identifier.epage408-
dc.identifier.isiWOS:000375416500014-
dc.publisher.placeChina-
dc.identifier.issnl1672-7681-

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