Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
11
pubmed:dateCreated
1996-3-18
pubmed:abstractText
The present report describes developmental, phenotypic and functional features of unconventional CD4+ TCR alpha beta lymphocytes. In C57BL/6 mice, the majority of liver lymphocytes expressing intermediate intensity of TCR alpha beta (TCR alpha beta int) are CD4+ NK1.1+ and express a highly restricted TCR V beta repertoire, dominated by V beta 8 with some contribution by V beta 7 and V beta 2. Although these cells express the CD4 co-receptor, they are present in H2-1 A beta (A beta)-/- gene disruption mutants but are markedly reduced in beta 2-microglobulin (beta 2m)-/- mutant mice and hence are beta 2m dependent. Thymocytes expressing the CD4+ NK1.1+ TCR alpha beta phenotype are also beta 2m contingent, suggesting that these two T lymphocyte populations are related. The CD4+ NK1.1+ TCR alpha beta lymphocytes in liver and thymus share several markers such as LFA-1+, CD44+, CD5+, LECAM-1- and IL-2R alpha-. The CD4+ NK1.1+ TCR alpha beta int liver lymphocytes were not detected in athymic nu/nu mice. We conclude that beta 2m expression is crucial for development of the CD4+ NK1.1+ TCR alpha beta int liver lymphocytes and that thymus plays a major role. CD4+ TCR alpha beta int liver lymphocytes were also identified in NK1.1- mouse strains, there lacking the NK1.1 marker. We assume that the NK1.1 molecule is a characteristic marker of the CD4+ TCR alpha beta int liver lymphocytes in NK1.1+ mouse strains, although its expression is not obligatory for their development. The liver lymphocytes from beta 2m+/-, but not from beta 2m-/-, mice are potent IL-4 producers in response to CD3 or TCR alpha beta engagement and the IL-4 production by liver lymphocytes was markedly reduced by treatment with anti-NK1.1 mAb. We conclude that the CD4+ NK1.1+ TCR alpha beta int liver lymphocytes are capable of producing IL-4 in response to TCR stimulation.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Ly, http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Surface, http://linkedlifedata.com/resource/pubmed/chemical/H-2 Antigens, http://linkedlifedata.com/resource/pubmed/chemical/Histocompatibility Antigens Class II, http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-4, http://linkedlifedata.com/resource/pubmed/chemical/Klrb1c protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Lectins, C-Type, http://linkedlifedata.com/resource/pubmed/chemical/NK Cell Lectin-Like Receptor..., http://linkedlifedata.com/resource/pubmed/chemical/Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Antigen, T-Cell..., http://linkedlifedata.com/resource/pubmed/chemical/beta 2-Microglobulin
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0953-8178
pubmed:author
pubmed:issnType
Print
pubmed:volume
7
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1729-39
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:8580071-Animals, pubmed-meshheading:8580071-Antigens, pubmed-meshheading:8580071-Antigens, Ly, pubmed-meshheading:8580071-Antigens, Surface, pubmed-meshheading:8580071-CD4 Lymphocyte Count, pubmed-meshheading:8580071-CD4-Positive T-Lymphocytes, pubmed-meshheading:8580071-Female, pubmed-meshheading:8580071-H-2 Antigens, pubmed-meshheading:8580071-Histocompatibility Antigens Class II, pubmed-meshheading:8580071-Immunophenotyping, pubmed-meshheading:8580071-Interleukin-4, pubmed-meshheading:8580071-Killer Cells, Natural, pubmed-meshheading:8580071-Lectins, C-Type, pubmed-meshheading:8580071-Liver, pubmed-meshheading:8580071-Male, pubmed-meshheading:8580071-Mice, pubmed-meshheading:8580071-Mice, Inbred Strains, pubmed-meshheading:8580071-Mice, Mutant Strains, pubmed-meshheading:8580071-Mice, Nude, pubmed-meshheading:8580071-NK Cell Lectin-Like Receptor Subfamily B, pubmed-meshheading:8580071-Protein Biosynthesis, pubmed-meshheading:8580071-Proteins, pubmed-meshheading:8580071-Receptors, Antigen, T-Cell, alpha-beta, pubmed-meshheading:8580071-Thymus Gland, pubmed-meshheading:8580071-beta 2-Microglobulin
pubmed:year
1995
pubmed:articleTitle
IL-4 producing CD4+ TCR alpha beta int liver lymphocytes: influence of thymus, beta 2-microglobulin and NK1.1 expression.
pubmed:affiliation
Department of Immunology, University of Ulm, Germany.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't