Journal of Leukocyte Biology · 2014 · 118 citations · 34 references
Life SciencesImmunologyMicrobiologyHost-pathogen InteractionsImmunology Of Infectious DiseasesInnate ImmunityImmune Responses To InfectionInnate Immune ResponseInnate Immune Signaling PathwaysNatural Killer Cell BiologyNatural Killer Cell FunctionCytotoxic Effector FunctionIntracellular Signaling PathwaysNatural Killer Cell CytotoxicityNatural Killer Cell Receptor Nkg2dNkg2 Receptor SignalingNkg2d-mediated RecognitionPerforin-mediated CytotoxicityPerforin-mediated Killing
Although the mechanisms underlying the cytotoxic effect of NK cells on tumor cells and intracellular bacteria have been studied extensively, it remains unclear how these cells kill extracellular bacterial pathogens. In this study, we examine how human NK cells kill Mycobacterium kansasii and M.tb. The underlying mechanism is contact dependent and requires two cytolytic proteins: perforin and granulysin. Mycobacteria induce enhanced expression of the cytolytic proteins via activation of the NKG2D/NCR cell-surface receptors and intracellular signaling pathways involving ERK, JNK, and p38 MAPKs. These results suggest that NK cells use similar cellular mechanisms to kill both bacterial pathogens and target host cells. This report reveals a novel role for NK cells, perforin, and granulysin in killing mycobacteria and highlights a potential alternative defense mechanism that the immune system can use against mycobacterial infection.
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An Antimicrobial Activity of Cytolytic T Cells Mediated by Granulysin
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