Cross-linking of VLA/CD29 molecule has a co-mitogenic effect with anti-CD3 on CD4 cell activation in serum-free culture system

Eur J Immunol. 1991 Feb;21(2):319-25. doi: 10.1002/eji.1830210212.

Abstract

In this study, we demonstrated that antibodies reactive with a common beta 1 subunit (CD29) of the VLA family of antigens could synergize with CD3 but not CD2 in inducing CD4 cell proliferation in a serum-free culture system. The extent of activation was similar to that obtained when CD4 cells were cultured with anti-CD3 plus fibronectin. The proliferative response induced via the CD3-CD29 pathway was associated with the interleukin (IL) 2 autocrine pathway, including IL 2 production and IL 2 receptor expression. Specifically, cross-linking of VLA-5, but not other members of the VLA family of antigens with the CD3 molecule induced strong CD4 cell activation. However, cross-linking of CD3 with other cell surface antigens such as CD4 did not induce CD4 cell activation in this serum-free culture system. The above results strongly suggest that the VLA/CD29 family of antigens may play an important role in regulating CD4 T cell activation via the CD3-T cell receptor pathway.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Antibodies, Monoclonal
  • Antigens, CD / physiology*
  • Antigens, Differentiation / physiology*
  • Antigens, Differentiation, T-Lymphocyte / physiology*
  • CD2 Antigens
  • CD3 Complex
  • CD4-Positive T-Lymphocytes / immunology*
  • Culture Media
  • Fibronectins / physiology
  • Humans
  • Integrin beta1
  • Interleukin-2 / biosynthesis
  • Lymphocyte Activation
  • Receptors, Antigen, T-Cell / physiology*
  • Receptors, Fibronectin
  • Receptors, Immunologic / physiology
  • Receptors, Interleukin-2 / biosynthesis
  • Receptors, Very Late Antigen / physiology*

Substances

  • Antibodies, Monoclonal
  • Antigens, CD
  • Antigens, Differentiation
  • Antigens, Differentiation, T-Lymphocyte
  • CD2 Antigens
  • CD3 Complex
  • Culture Media
  • Fibronectins
  • Integrin beta1
  • Interleukin-2
  • Receptors, Antigen, T-Cell
  • Receptors, Fibronectin
  • Receptors, Immunologic
  • Receptors, Interleukin-2
  • Receptors, Very Late Antigen