NOTCH1 Can Initiate NF-κB Activation via Cytosolic Interactions with Components of the T Cell Signalosome.
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Shin HM
Program in Molecular and Cellular Biology, University of Massachusetts/Amherst , Amherst, MA , USA.
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Tilahun ME
Department of Veterinary and Animal Sciences, University of Massachusetts/Amherst , Amherst, MA , USA.
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Cho OH
Department of Veterinary and Animal Sciences, University of Massachusetts/Amherst , Amherst, MA , USA.
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Chandiran K
Program in Molecular and Cellular Biology, University of Massachusetts/Amherst , Amherst, MA , USA.
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Kuksin CA
Department of Veterinary and Animal Sciences, University of Massachusetts/Amherst , Amherst, MA , USA.
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Keerthivasan S
Program in Molecular Biology, Loyola University Medical Center , Maywood, IL , USA.
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Fauq AH
Chemical Synthesis Core Facility, Mayo Clinic , Jacksonville, FL , USA.
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Golde TE
Center for Translational Research in Neurodegenerative Disease, University of Florida , Gainesville, FL , USA ; Department of Neuroscience, College of Medicine, University of Florida , Gainesville, FL , USA.
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Miele L
Department of Medicine and Pharmacology, University of Mississippi Medical Center, University of Mississippi Cancer Institute , Jackson, MS , USA.
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Thome M
Department of Biochemistry, Center of Immunity and Infection, University of Lausanne , Epalinges , Switzerland.
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Osborne BA
Program in Molecular and Cellular Biology, University of Massachusetts/Amherst , Amherst, MA , USA ; Department of Veterinary and Animal Sciences, University of Massachusetts/Amherst , Amherst, MA , USA.
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Minter LM
Program in Molecular and Cellular Biology, University of Massachusetts/Amherst , Amherst, MA , USA ; Department of Veterinary and Animal Sciences, University of Massachusetts/Amherst , Amherst, MA , USA.
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Published in:
- Frontiers in immunology. - 2014
English
T cell stimulation requires the input and integration of external signals. Signaling through the T cell receptor (TCR) is known to induce formation of the membrane-tethered CBM complex, comprising CARMA1, BCL10, and MALT1, which is required for TCR-mediated NF-κB activation. TCR signaling has been shown to activate NOTCH proteins, transmembrane receptors also implicated in NF-κB activation. However, the link between TCR-mediated NOTCH signaling and early events leading to induction of NF-κB activity remains unclear. In this report, we demonstrate a novel cytosolic function for NOTCH1 and show that it is essential to CBM complex formation. Using a model of skin allograft rejection, we show in vivo that NOTCH1 acts in the same functional pathway as PKCθ, a T cell-specific kinase important for CBM assembly and classical NF-κB activation. We further demonstrate in vitro NOTCH1 associates physically with PKCθ and CARMA1 in the cytosol. Unexpectedly, when NOTCH1 expression was abrogated using RNAi approaches, interactions between CARMA1, BCL10, and MALT1 were lost. This failure in CBM assembly reduced inhibitor of kappa B alpha phosphorylation and diminished NF-κB-DNA binding. Finally, using a luciferase gene reporter assay, we show the intracellular domain of NOTCH1 can initiate robust NF-κB activity in stimulated T cells, even when NOTCH1 is excluded from the nucleus through modifications that restrict it to the cytoplasm or hold it tethered to the membrane. Collectively, these observations provide evidence that NOTCH1 may facilitate early events during T cell activation by nucleating the CBM complex and initiating NF-κB signaling.
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Open access status
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gold
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https://sonar.ch/global/documents/281174
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