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PMID: 10066342 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

4-1BB costimulation promotes human T cell adhesion to fibronectin.

Cellular immunology ·Vol. 192 ·No. 1 ·1999-02-25 ·Pages 13-23

Kim YJ, Mantel PL, June CH, Kim SH, Kwon BS

Abstract

CD28 and 4-1BB (CD137) are costimulatory molecules for T cells. In this study we investigated the role of 4-1BB in T cell adhesion to fibronectin (FN). Unlike CD28, 4-1BB is present in only a small subset of T cells prepared from fresh human peripheral blood mononuclear cells, but was induced after prolonged TCR/CD28 activation in vitro. 4-1BB-expressing T cells were characteristically unique in their strong responsiveness to FN. Anti-4-1BB cross-linking synergized CD28 costimulation by lowering the threshold of CD3 signal required for CD28-mediated maximal proliferative response. In addition to increasing proliferative responses, 4-1BB promoted T cell adhesion to FN in the presence of CD28 costimulation. 4-1BB-mediated cell adhesion to FN was blocked by anti-beta1 integrin, suggesting that 4-1BB mediates beta1 integrin activation. The role of 4-1BB in inducing CD4(+) T cell adhesion to FN was confirmed by showing that the human leukemic CD4(+) T cell line, Jurkat, when transfected with cDNA encoding 4-1BB, became adherent to FN with anti-4-1BB stimulation. Taken together, our results suggest that 4-1BB-promoted T cell adhesion to extracellular matrix proteins is an important postactivation process for T cell migration.

MeSH Terms
Antigens, CD CD28 Antigens/metabolism CD3 Complex/metabolism CD4-Positive T-Lymphocytes/metabolism,physiology Cell Adhesion Drug Synergism Fibronectins/metabolism Humans Integrin beta1/metabolism Jurkat Cells Lymphocyte Activation Receptors, Nerve Growth Factor/genetics,physiology Receptors, Tumor Necrosis Factor/genetics,physiology Signal Transduction Tumor Necrosis Factor Receptor Superfamily, Member 9
Chemicals
Antigens, CD CD28 Antigens CD3 Complex Fibronectins Integrin beta1 Receptors, Nerve Growth Factor Receptors, Tumor Necrosis Factor TNFRSF9 protein, human Tumor Necrosis Factor Receptor Superfamily, Member 9
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Kim Y J
Department of Microbiology and Immunology, and Walther Oncology Center, Indiana University School of Medicine, 635 Barnhill Drive, Indianapolis, Indiana 46202-5120, USA.
Mantel P L
June C H
Kim S H
Kwon B S
Article Info
Journal
Cellular immunology
Abbr.
Cell Immunol
ISSN
0008-8749
Published
1999-02-25
Pages
13-23
Language
English
Region
Netherlands
NLM ID
1246405
Subset
IM
Grants
NIAID NIH HHS · AI 28125 · United States
NIAID NIH HHS · AI 42379 · United States
NIDCR NIH HHS · DE 12156 · United States
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