Related Experiment Video
Updated: Aug 10, 2026

Phospho Flow Cytometry with Fluorescent Cell Barcoding for Single Cell Signaling Analysis and Biomarker Discovery
Published on: October 4, 2018
Protein kinase A-mediated phosphorylation of the T-cell surface antigen CD27
K Sugita1, J D Dasgupta, Y Nojima
1Division of Tumor Immunology, Dana-Farber Cancer Institute, Boston, MA 02115.
Abstract:
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.
Insights
CD27, a T-cell surface antigen, is rapidly phosphorylated during T-cell activation. This process is primarily mediated by cyclic AMP-protein kinase A, highlighting a novel signaling pathway for T-cell surface molecules.
Area of Science:
- Immunology
- Cell Signaling
Background:
- CD27 is a T-cell surface antigen belonging to a receptor family including TNF receptors and Fas.
- The precise function of CD27 in T-cell activation remains largely undefined.
- Experimental evidence suggests CD27 plays a significant role in T-cell activation processes.
Purpose of the Study:
- To investigate the phosphorylation of CD27 during T-cell activation.
- To identify the key kinases involved in CD27 phosphorylation.
- To elucidate the signaling pathways regulating CD27 phosphorylation.
Main Methods:
- Stimulation of T-cells with cyclic AMP-inducing agents (forskolin, 8-bromo-cAMP) and PMA.
- Analysis of CD27 phosphorylation levels.
- Inhibition of kinase activity using H-8 (cyclic nucleotide-dependent kinase inhibitor) and staurosporine (protein kinase C inhibitor).
- T-cell activation via CD2 or CD3 pathways.
Main Results:
- CD27 undergoes rapid hyperphosphorylation upon stimulation with cyclic AMP-inducing agents and PMA.
- T-cell activation via CD2/CD3 pathways leads to increased CD27 phosphorylation.
- CD27 phosphorylation is significantly suppressed by H-8, but only slightly by staurosporine.
- These findings implicate protein kinase A as a key regulator of CD27 phosphorylation.
Conclusions:
- CD27 phosphorylation is regulated by the cyclic AMP-protein kinase A pathway.
- This study identifies CD27 as the first T-cell surface antigen phosphorylated via this specific pathway.
- The findings provide new insights into the signaling mechanisms governing T-cell activation and CD27 function.
Related Concept Videos
Amplifying Signals via Enzymatic Cascade
MAPK Signaling Cascades
The JAK-STAT Signaling Pathway
PI3K/mTOR/AKT Signaling Pathway
cAMP-dependent Protein Kinase Pathways
T Cell Activation and Clonal Selection
Naive T cells that have not yet encountered an antigen express two primary CD...

