Science Signaling · 2012 · 38 citations · 43 references
Life SciencesImmunologyMolecular BiologyApoptosisCell SignalingEndocytosisApoptosis In Immune CellsApoptosis RegulationApoptotic SignalingClathrin-mediated EndocytosisDeath ReceptorsReceptor-mediated EndocytosisClathrin-mediated Endocytosis RegulationImmune Effector Cell FunctionInnate Immune Cell FunctionLysosomal Degradation PathwaysPhosphoinositide 3-Kinase PathwayPhosphoinositide 3-Kinase SignalingRenal ApoptosisScavenger Receptors
T cell immunoglobulin and mucin domain (TIM) proteins are cell-surface signaling receptors in T cells and scavenger receptors in antigen-presenting cells and kidney tubular epithelia. Here, we demonstrated a function for TIM proteins in mediating the degradation of NUR77, a nuclear receptor implicated in apoptosis and cell survival. TIM proteins interacted with and mediated the lysosomal degradation of NUR77 in a phosphoinositide 3-kinase-dependent pathway. We also showed dynamic cycling of TIM-1 to and from the cell surface through clathrin-dependent constitutive endocytosis. Blocking this process or mutating the phosphatidylserine-binding pocket in TIM-1 abrogated TIM-1-mediated degradation of NUR77. In an in vitro model of kidney injury, silencing TIM-1 increased NUR77 abundance and decreased epithelial cell survival. These results show that TIM proteins may affect immune cell function and the response of the kidney to injury.
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