Expression and co-stimulatory function of B7-2 on murine CD4+ T cells
β Scribed by Rie Hakamada-Taguchi; Takuma Kato; Hiroshi Ushijima; Masaaki Murakami; Toshimitsu Uede; Hideo Nariuchi
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 207 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0014-2980
No coin nor oath required. For personal study only.
β¦ Synopsis
Co-stimulatory signals mediated by the interaction of B7-1/B7-2 with CD28 are important for the activation of CD4 + T cells stimulated with antigen on antigen-presenting cells. There are controversies about the expression and function of B7-1/B7-2 on CD4 + T cells. The aim of this study was to analyze the expression of B7-1/B7-2 on naive and memory CD4 + T cells and the co-stimulatory function in the activation of naive CD4 + T cells stimulated by TCR ligation. Present results indicate that memory CD4 + T cells express B7-2 molecules on their surface, whereas naive CD4 + T cells do not. Neither memory nor naive CD4 + T cells expressed B7-1 molecule on their surface, although B7-1 mRNA was faintly expressed in memory T cells. B7-2 molecules expressed on memory T cells co-stimulated CD4 + naive T cells stimulated with plate-coated anti-CD3 to produce IL-2. Naive CD4 + T cells were shown to express B7-2 after co-stimulation with B7-2 and TCR ligation, because the naive T cells stimulated with anti-CD3 and B7-2CHO expressed B7-2 on their surface, although it remained to be studied whether the co-stimulation with B7-2 directly induced B7-2 expression on naive T cells. Our present results indicate that memory CD4 + T cells play some role in the activation of naive CD4 + T cells through the co-stimulation with B7-2 molecules.
π SIMILAR VOLUMES
## Abstract ## Objective Deficiency of decayβaccelerating factor 1 (termed Daf1 in mice) has been shown to exacerbate autoimmunity, and recent studies have suggested that this may be explained by Daf1 acting as a regulator of T cell immunity. The aim of this study was to determine whether Daf1 exp
The pan-NK cell marker NK1.1, present in some mouse strains, is also found on a subset of TCRalphabeta+ lymphocytes termed NKT cells. These cells are primarily CD4+ or CD4-CD8- (double negative, DN), and both NKT subpopulations contain cells reactive with the MHC class I-like molecule CD1d. Murine N
We investigated the T cell population in the afferent lymph and the peripheral blood with regard to expression of activation, adhesion and co-stimulatory molecules and cytokine profile by immunohistochemistry and flow cytometry. The majority of the lymphoid cell population in the afferent lymph were