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The mouse vitronectin receptor is a T cell activation antigen
K Moulder1, K Roberts, E M Shevach
1Biological Resources Branch, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892.
The Journal of Experimental Medicine
|February 1, 1991
Summary
The murine vitronectin receptor (VNR) is identified on lymphoid cells, binding extracellular matrix proteins. This finding suggests VNR plays a key role in mouse T cell functions and activation.
Area of Science:
- Immunology
- Cell Biology
- Molecular Biology
Background:
- The T cell activation antigen, recognized by monoclonal antibody H9.2B8, was previously uncharacterized in mice.
- Vitronectin receptor (VNR) is known to bind extracellular matrix proteins via the RGD sequence.
- The function of VNR in T cell activation has been suggested by recent studies.
Purpose of the Study:
- To identify the murine homologue of the vitronectin receptor (VNR) on T cell activation antigens.
- To investigate the expression of VNR on various lymphoid cells.
- To determine the binding capabilities and potential role of VNR in T cell functions.
Main Methods:
- Monoclonal antibody H9.2B8 was used to identify the T cell activation antigen.
- Expression analysis was performed on T cell lines, tumors, and splenocytes.
- Binding assays were conducted with extracellular matrix proteins like fibronectin, fibrinogen, and vitronectin.
Main Results:
- The T cell activation antigen recognized by H9.2B8 is the murine homologue of VNR.
- VNR is expressed on T cell lines, tumors, and Con A-activated splenocytes, but not resting T cells.
- VNR binds fibronectin, fibrinogen, and vitronectin via the RGD sequence; no novel beta chains were found pairing with the VNR alpha chain.
Conclusions:
- Vitronectin receptor (VNR) is expressed on murine lymphoid cells.
- VNR's ability to bind extracellular matrix proteins suggests a role in T cell adhesion and migration.
- VNR may function as an accessory molecule in T cell activation, highlighting its importance in mouse T cell immunity.