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Cited by 288

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Activation of CD4 cells by fibronectin and anti-CD3 antibody. A synergistic effect mediated by the VLA-5 fibronectin receptor complex.

Open access
Matsuyama, T, Yamada, A, Kay, J, Yamada, K M, Akiyama, S K, Schlossman, S F, Morimoto, C·1989·The Journal of experimental medicine

Abstract

In this study, fibronectin synergized with anti-CD3 antibody to promote CD4 cell proliferation in a serum-free culture system. The cell-adhesive domain plus additional regions of the fibronectin molecule are involved in this synergy. Anti4B4(CDw29) antibody blocked the activation of CD4 cells in this system. Furthermore, it is the VLA-5 protein within the set of molecules recognized by anti-4B4 that serves as a fibronectin receptor on the CD4 lymphocytes. The VLA-5 fibronectin receptor was mainly expressed on CD4+ CD45R-CDw29+ cells and may in part contribute to the unique function of these cells.

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Metadata

Authors
Matsuyama, T., Yamada, A., Kay, J., Yamada, K. M., Akiyama, S. K., Schlossman, S. F., & Morimoto, C.
Venue
The Journal of experimental medicine
Published
1989-10-01
Volume
170
Issue
4
Pages
1133-1148
ISSN
  • 0022-1007 (ISSN-L)
  • 1540-9538
OpenAlex
W2052083000
Cited by
288
References
0
FWCI
8.30
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Activation of CD4 cells by fibronectin and anti-CD3 antibody. A synergistic effect mediated by the VLA-5 fibronectin receptor complex. https://app.cochat.ai/papers/10.1084/jem.170.4.1133
The paper
Matsuyama, T., Yamada, A., Kay, J., Yamada, K. M., Akiyama, S. K., Schlossman, S. F., & Morimoto, C. (1989). Activation of CD4 cells by fibronectin and anti-CD3 antibody. A synergistic effect mediated by the VLA-5 fibronectin receptor complex. The Journal of experimental medicine. https://doi.org/10.1084/jem.170.4.1133

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.