Linked Life Data

21235539

Source:http://linkedlifedata.com/resource/pubmed/id/21235539

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2011-3-11
pubmed:abstractText
Our previous study demonstrated that T helper (Th) cells from patients with rheumatoid arthritis (RA) display an altered expression profile of Notch receptors and enhanced activation of Notch signalling. The aim of this study was to investigate the role of distinct Notch receptors and ligands in the activation and differentiation of collagen II (CII)-reactive Th cells upon antigen-specific restimulation. Spleen mononuclear cells (SMNCs) from CII-immunized DBA/1J mice were restimulated by culturing with CII. CII-specific proliferation and differentiation of T cells were determined by tritiated thymidine ((3) [H]-TdR) incorporation and flow cytometric analysis, respectively. The mRNA expression of Notch receptors and Hes1 was assessed by real-time polymerase chain reaction (PCR). There was a clear increase in the percentage of Th1 cells and Th17 cells after CII restimulation. No significant difference was observed in the percentage of regulation T cells (T(reg) ) in SMNCs with or without CII restimulation. CII restimulation induced up-regulated transcript levels of Hes1 in CII-reactive CD4(+) T cells. The mRNA level of Notch3 was also up-regulated significantly, while the levels of the other three Notch receptors were not increased. Inhibition of Notch signalling by N-[N-(3,5-difluorophenacetyl)-L-alanyl]-S-phenylglycine t-butyl ester (DAPT) and Notch3 antibody decreased the collagen-specific T cell proliferation and attenuated Th1- and Th17-type responses, while treatment with Notch ligand Delta-like 1 promoted such a response. The present study demonstrates that Notch signalling is engaged in CII-specific Th1- and Th17-type expansion in which Notch3 and Delta-like1 were involved. Selective inhibition of Notch signalling mediated by Notch3 or Delta-like1 may offer a new strategy for the treatment of RA.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
1365-2249
pubmed:author
pubmed:copyrightInfo
© 2011 The Authors. Clinical and Experimental Immunology © 2011 British Society for Immunology.
pubmed:issnType
Electronic
pubmed:volume
164
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
66-71
pubmed:meshHeading
pubmed-meshheading:21235539-Animals, pubmed-meshheading:21235539-Antibodies, pubmed-meshheading:21235539-Cell Proliferation, pubmed-meshheading:21235539-Cells, Cultured, pubmed-meshheading:21235539-Collagen Type II, pubmed-meshheading:21235539-Dipeptides, pubmed-meshheading:21235539-Flow Cytometry, pubmed-meshheading:21235539-Gene Expression, pubmed-meshheading:21235539-Immunoglobulin Fc Fragments, pubmed-meshheading:21235539-Intercellular Signaling Peptides and Proteins, pubmed-meshheading:21235539-Male, pubmed-meshheading:21235539-Mice, pubmed-meshheading:21235539-Mice, Inbred DBA, pubmed-meshheading:21235539-Receptors, Notch, pubmed-meshheading:21235539-Recombinant Fusion Proteins, pubmed-meshheading:21235539-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:21235539-Signal Transduction, pubmed-meshheading:21235539-T-Lymphocytes, pubmed-meshheading:21235539-T-Lymphocytes, Regulatory, pubmed-meshheading:21235539-Th1 Cells, pubmed-meshheading:21235539-Th17 Cells
pubmed:year
2011
pubmed:articleTitle
Engagement of activated Notch signalling in collagen II-specific T helper type 1 (Th1)- and Th17-type expansion involving Notch3 and Delta-like1.
pubmed:affiliation
Central Laboratory, Department of Laboratory Medicine, Affiliated Hospital of Jiangsu University Pathogenic Biology Immunology, School of Medical Science and Laboratory Medicine, Jiangsu University, Zhenjiang Department of Laboratory Medicine, Jiangyin People's Hospital, Jiangyin, China. jiaozhijun@yahoo.com.cn
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't