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Publication : Timed Regulation of 3BP2 Induction Is Critical for Sustaining CD8<sup>+</sup> T Cell Expansion and Differentiation.

First Author  Dimitriou ID Year  2018
Journal  Cell Rep Volume  24
Issue  5 Pages  1123-1135
PubMed ID  30067970 Mgi Jnum  J:270763
Mgi Id  MGI:6278700 Doi  10.1016/j.celrep.2018.06.075
Citation  Dimitriou ID, et al. (2018) Timed Regulation of 3BP2 Induction Is Critical for Sustaining CD8(+) T Cell Expansion and Differentiation. Cell Rep 24(5):1123-1135
abstractText  Successful anti-viral response requires the sustained activation and expansion of CD8(+) T cells for periods that far exceed the time limit of physical T cell interaction with antigen-presenting cells (APCs). The expanding CD8(+) T cell pool generates the effector and memory cell populations that provide viral clearance and long-term immunity, respectively. Here, we demonstrate that 3BP2 is recruited in cytoplasmic microclusters and nucleates a signaling complex that facilitates MHC:peptide-independent activation of signaling pathways downstream of the TCR. We show that induction of the adaptor molecule 3BP2 is a sensor of TCR signal strength and is critical for sustaining CD8(+) T cell proliferation and regulating effector and memory differentiation.
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