IndraLab

Statements



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"To address whether proteasomal or lysosomal degradation is involved in US9 mediated MAVS reduction, HEK293T cells were treated with either MG132, a proteasome inhibitor, or chloroquine, a lysosome inhibitor."

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"In the meantime, the treatment of MG132, a proteasome inhibitor, rescued CORT caused decrease of MAVS in virus exposed A549 cells."

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"Treatment with a proteasome inhibitor MG132 effectively blocked MAVS degradation."

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"Addition of the proteasome inhibitor MG132 potently inhibited the cleavage of MAVS relative to cells treated with apoptosis-inducers alone (XREF_FIG)."

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"Finally, in agreement with confocal data, addition of MG132 to STS incubated cells reverses the change in MAVS localization, the majority being found in the membrane fraction as expected (XREF_FIG)."