Direct bacterial protein PAMP recognition by human NK cells involves TLRs and triggers alpha-defensin production
- PMID: 15166032
- DOI: 10.1182/blood-2003-08-2820
Direct bacterial protein PAMP recognition by human NK cells involves TLRs and triggers alpha-defensin production
Abstract
Although human CD56(+)CD3(-) natural killer (NK) cells participate in immune responses against microorganisms, their capacity to directly recognize and be activated by pathogens remains unclear. These cells encode members of the Toll-like receptor (TLR) family, involved in innate cell activation on recognition of pathogen-associated molecular patterns (PAMPs). We therefore evaluated whether the 2 bacterial protein PAMPs, the outer membrane protein A from Klebsiella pneumoniae (KpOmpA) and flagellin, which signal through TLR2 and TLR5, respectively, may directly stimulate human NK cells. These proteins induce interferon-gamma (IFN-gamma) production by NK cells and synergize with interleukin-2 (IL-2) and proinflammatory cytokines in PAMP-induced activation. Similar results were obtained using CD56(+)CD3(+) (NKR-expressing) T cells. NK cells from TLR2(-/-) mice fail to respond to KpOmpA, demonstrating TLR involvement in this effect. Defensins are antimicrobial peptides expressed mainly by epithelial cells and neutrophils that disrupt the bacterial membrane, leading to pathogen death. We show that NK cells and NKR-expressing T cells constitutively express alpha-defensins and that KpOmpA and flagellin rapidly induce their release. These data demonstrate for the first time that highly purified NK cells directly recognize and respond to pathogen components through TLRs and evidence defensins as a novel and direct cytotoxic pathway involved in NK cell-mediated protection against microorganisms.
Similar articles
-
Type 1 cytokine/chemokine production by mouse NK cells following activation of their TLR/MyD88-mediated pathways.Int Immunol. 2007 Mar;19(3):311-20. doi: 10.1093/intimm/dxl148. Epub 2007 Feb 7. Int Immunol. 2007. PMID: 17289654
-
TLR7/8-mediated activation of human NK cells results in accessory cell-dependent IFN-gamma production.J Immunol. 2005 Aug 1;175(3):1636-42. doi: 10.4049/jimmunol.175.3.1636. J Immunol. 2005. PMID: 16034103
-
Dendritic cells and NK cells stimulate bystander T cell activation in response to TLR agonists through secretion of IFN-alpha beta and IFN-gamma.J Immunol. 2005 Jan 15;174(2):767-76. doi: 10.4049/jimmunol.174.2.767. J Immunol. 2005. PMID: 15634897
-
Toll-Like Receptors in Natural Killer Cells and Their Application for Immunotherapy.J Immunol Res. 2020 Jan 4;2020:2045860. doi: 10.1155/2020/2045860. eCollection 2020. J Immunol Res. 2020. PMID: 32377528 Free PMC article. Review.
-
Toll-like receptors as adjuvant receptors.Biochim Biophys Acta. 2002 Feb 13;1589(1):1-13. doi: 10.1016/s0167-4889(01)00182-3. Biochim Biophys Acta. 2002. PMID: 11909637 Review.
Cited by
-
Toll-like receptors expression and interferon-γ production by NK cells in human sepsis.Crit Care. 2012 Oct 25;16(5):R206. doi: 10.1186/cc11838. Crit Care. 2012. PMID: 23098236 Free PMC article.
-
Monocytes and the 38kDa-antigen of mycobacterium tuberculosis modulate natural killer cell activity and their cytolysis directed against ovarian cancer cell lines.BMC Cancer. 2012 Oct 4;12:451. doi: 10.1186/1471-2407-12-451. BMC Cancer. 2012. PMID: 23036052 Free PMC article.
-
Requirement and redundancy of the Src family kinases Fyn and Lyn in perforin-dependent killing of Cryptococcus neoformans by NK cells.Infect Immun. 2013 Oct;81(10):3912-22. doi: 10.1128/IAI.00533-13. Epub 2013 Aug 5. Infect Immun. 2013. PMID: 23918783 Free PMC article.
-
Between adaptive and innate immunity: TLR4-mediated perforin production by CD28null T-helper cells in ankylosing spondylitis.Arthritis Res Ther. 2005;7(6):R1412-20. doi: 10.1186/ar1840. Epub 2005 Oct 18. Arthritis Res Ther. 2005. PMID: 16277694 Free PMC article.
-
Synovial fluid α-defensin in the diagnosis of periprosthetic joint infection: the lateral flow test is an effective intraoperative detection method.J Orthop Surg Res. 2019 Aug 28;14(1):274. doi: 10.1186/s13018-019-1320-9. J Orthop Surg Res. 2019. PMID: 31455372 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials