Protein kinase A-mediated phosphorylation of the T-cell surface antigen CD27

• Published in: Immunology Vol. 80; no. 2; pp. 217 - 221
• Main Authors: SUGITA, K, DASGUPTA, J. D, NOJIMA, Y, AGEMATSU, K, SCHLOSSMAN, S. F, MORIMOTO, C
• Format: Journal Article
• Language: English
• Published: Oxford Blackwell 01.10.1993
• Subjects: 8-Bromo Cyclic Adenosine Monophosphate - pharmacology; Biological and medical sciences; Cells, Cultured; Colforsin - pharmacology; Cyclic AMP-Dependent Protein Kinases - immunology; Electrophoresis, Polyacrylamide Gel; Fundamental and applied biological sciences. Psychology; Fundamental immunology; Humans; Immunobiology; Lymphocyte Activation - physiology; Lymphoid cells: ontogeny, maturation, markers, receptors, circulation and recirculation; Phosphorylation; T-Lymphocytes - immunology; Tumor Necrosis Factor Receptor Superfamily, Member 7 - immunology; Tumor Necrosis Factor Receptor Superfamily, Member 7 - metabolism; Human; Phosphorylation; Enzymatic activity; Enzyme; Protein kinase; Transferases; T-Lymphocyte; Biological marker; Activation; Cell surface
• ISSN: 0019-2805; 1365-2567

CD27 is a T-cell surface antigen expressed on the majority of peripheral T cells and belongs to a newly defined receptor family including the low-affinity nerve growth factor receptor, tumour necrosis factor (TNF) receptors, the B-cell activation antigen CD40, and the Fas antigen. Although the function of CD27 has not been defined, several experimental observations support the notion that this molecule plays an important role in the process of T-cell activation. In this paper, we have demonstrated that a rapid hyperphosphorylation of CD27 is induced by a cyclic AMP-inducing agent, forskolin, and a membrane-permeable cAMP analogue, 8-bromo-cAMP, as well as phorbol 12-myristate 13-acetate (PMA). In addition, increased phosphorylation of CD27 in T-cell activation either via CD2 or CD3 pathways was strongly suppressed by a cyclic nucleotide-dependent kinase inhibitor, H-8, but only slightly by a protein kinase C inhibitor, staurosporine. These results suggest that protein kinase A might be a key kinase responsible for CD27 phosphorylation in the process of T-cell activation. CD27 is the first T-cell surface antigen demonstrated to be phosphorylated by the cyclic AMP-protein kinase A-mediated pathway.