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PMID: 1670606 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Activation of human CD4 T lymphocytes. Interaction of fibronectin with VLA-5 receptor on CD4 cells induces the AP-1 transcription factor.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 146 ·No. 1 ·1991-01-01 ·Pages 53-6

Yamada A, Nikaido T, Nojima Y, Schlossman SF, Morimoto C

Abstract

Fibronectin synergized with anti-CD3 antibody to promote CD4 cell proliferation in a serum-free culture system whereas no proliferation was observed when CD4 cells were cultured with anti-CD3 alone or fibronectin alone. In addition, anti-CD29 (integrin beta 1) as well as anti-VLA-5 (human fibronectin receptor) antibodies blocked this CD4 cell activation in this system. Although anti-CD3 alone or fibronectin alone cannot induce IL-2 message by CD4 cells, the combination of anti-CD3 plus fibronectin induced IL-2 message by CD4 cells. In an analysis of the molecular mechanism by which IL-2 message was generated, we showed that a fibronectin-VLA-5 fibronectin receptor interaction may contribute an independent signal distinct from the CD3 pathway of activation by the induction of an AP-1 transcriptional factor. Thus the VLA-5 fibronectin receptor on CD4 cells can play a complementary role in CD3-TCR-mediated signal transduction through its interaction with fibronectin.

MeSH Terms
Antibodies, Monoclonal Antigens, Differentiation, T-Lymphocyte/physiology CD3 Complex CD4-Positive T-Lymphocytes/immunology DNA-Binding Proteins/biosynthesis Fibronectins/physiology Gene Expression Humans In Vitro Techniques Interleukin-2/genetics Lymphocyte Activation Protein Kinase C/metabolism Proto-Oncogene Proteins c-jun Receptors, Antigen, T-Cell/physiology Receptors, Fibronectin Receptors, Immunologic/physiology Receptors, Interleukin-2/metabolism Receptors, Very Late Antigen/physiology Transcription Factors/biosynthesis
Chemicals
Antibodies, Monoclonal Antigens, Differentiation, T-Lymphocyte CD3 Complex DNA-Binding Proteins Fibronectins Interleukin-2 Proto-Oncogene Proteins c-jun Receptors, Antigen, T-Cell Receptors, Fibronectin Receptors, Immunologic Receptors, Interleukin-2 Receptors, Very Late Antigen Transcription Factors Protein Kinase C
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Yamada A
Division of Tumor Immunology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115.
Nikaido T
Nojima Y
Schlossman S F
Morimoto C
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
1991-01-01
Pages
53-6
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
Grants
NIAID NIH HHS · AI-12069 · United States
NIAMS NIH HHS · AR-33713 · United States
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