Literature DB >> 25139289

NK cells kill mycobacteria directly by releasing perforin and granulysin.

Chia-Chen Lu1, Ting-Shu Wu2, Ya-Jing Hsu3, Chih-Jung Chang4, Chuan-Sheng Lin3, Ju-Hsin Chia5, Tsu-Lan Wu5, Tsung-Teng Huang6, Jan Martel7, David M Ojcius8, John D Young9, Hsin-Chih Lai10.   

Abstract

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.
© 2014 Society for Leukocyte Biology.

Entities:  

Keywords:  NCR; NKG2D; antibacterial activity; innate immunity; tuberculosis

Mesh:

Substances:

Year:  2014        PMID: 25139289     DOI: 10.1189/jlb.4A0713-363RR

Source DB:  PubMed          Journal:  J Leukoc Biol        ISSN: 0741-5400            Impact factor:   4.962


  29 in total

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