SHP-1 and SHP-2 Associate with Immunoreceptor Tyrosine-Based Switch Motif of Programmed Death 1 upon Primary Human T Cell Stimulation, but Only Receptor Ligation Prevents T Cell Activation
Cancer Research Institute · University of Pennsylvania · +1 more institution
Abstract
To study the cis- and trans-acting factors that mediate programmed death 1 (PD-1) signaling in primary human CD4 T cells, we constructed a chimeric molecule consisting of the murine CD28 extracellular domain and human PD-1 cytoplasmic tail. When introduced into CD4 T cells, this construct mimics the activity of endogenous PD-1 in terms of its ability to suppress T cell expansion and cytokine production. The cytoplasmic tail of PD-1 contains two structural motifs, an ITIM and an immunoreceptor tyrosine-based switch motif (ITSM). Mutation of the ITIM had little effect on PD-1 signaling or functional activity. In contrast, mutation of the ITSM abrogated the ability of PD-1 to block cytokine synthesis and to limit…
Citation impact
- FWCI
- 6.81
- Percentile
- 100%
- References
- 58
Authors
5- JMJens M. ChemnitzCorresponding
Cancer Research Institute, University of Pennsylvania
- RVRichard V. Parry
Cancer Research Institute, University of Pennsylvania
- KEKim E. Nichols
Children's Hospital of Philadelphia
- CHCarl H. June
Cancer Research Institute, University of Pennsylvania
- JLJames L. Riley
Cancer Research Institute, University of Pennsylvania
Topics & keywords
- Immunoreceptor tyrosine-based activation motif
- CD28
- Cell biology
- T-cell receptor
- Proto-oncogene tyrosine-protein kinase Src
- Protein tyrosine phosphatase
- T cell
- SH2 domain
- Good health and well-being