NKG2D and Natural Cytotoxicity Receptors Are Involved in Natural Killer Cell Interaction with Self-Antigen Presenting Cells and Stromal Cells

2007 ◽  
Vol 1109 (1) ◽  
pp. 47-57 ◽  
Author(s):  
A. POGGI ◽  
C. PREVOSTO ◽  
M. ZANCOLLI ◽  
P. CANEVALI ◽  
A. MUSSO ◽  
...  
2006 ◽  
Vol 13 (2-4) ◽  
pp. 325-336 ◽  
Author(s):  
Alessandro Poggi ◽  
Maria Raffaella Zocchi

Human natural killer (NK) lymphocytes should not damage autologous cells due to the engagement of inhibitory receptor superfamily (IRS) members by HLA-I. Nevertheless, NK cells kill self cells expressing low levels or lacking HLA-I, as it may occur during viral infections (missing-self hypothesis). Herein, we show that human NK cells can be activated upon binding with self antigen presenting cells or stromal cells despite the expression of HLA-I. Indeed, NK cells can kill and produce pro-inflammatory and regulating cytokines as IFN-γ, TNF-α and IL10 during interaction with autologous dendritic cells or bone marrow stromal cells or skin fibroblasts. The killing of antigen presenting and stromal cells is dependent on LFA1/ICAM1 interaction. Further, the natural cytotoxicity receptors (NCR) NKp30 and NKp46 are responsible for the delivery of lethal hit to DC, whereas NKG2D activating receptor, the ligand of the MHC-related molecule MIC-A and the UL16 binding protein, is involved in stromal cell killing. These findings indicate that different activating receptors are involved in cell to self cell interaction. Finally, NK cells can revert the veto effect of stromal cells on mixed lymphocyte reaction further supporting the idea that NK cells may alter the interaction between T lymphocytes and microenvironment leading to autoreactivity.


2015 ◽  
Vol 5 (1) ◽  
pp. e1041701 ◽  
Author(s):  
Anna Martner ◽  
Anna Rydström ◽  
Rebecca E Riise ◽  
Johan Aurelius ◽  
Harald Anderson ◽  
...  

1995 ◽  
Vol 60 (3) ◽  
pp. 281-286 ◽  
Author(s):  
MARGARITA SALCEDO ◽  
FETTER HOGLUND ◽  
HANS-GUSTAF LJUNGGREN

Blood ◽  
2000 ◽  
Vol 96 (1) ◽  
pp. 259-263 ◽  
Author(s):  
Chun-Xiang Wang ◽  
Bernard C. Fisk ◽  
Madhuri Wadehra ◽  
Helen Su ◽  
Jonathan Braun

Abstract Fizzy-related (fzr) is a recently identified 7WD domain family member implicated in cell cycle regulation of Drosophila and yeast. In this study, the murine homologue of fzr was isolated by suppression subtractive hybridization as a gene with decreased expression during malignant progression of a murine B-lymphoma cell line. Retroviral overexpression of fzr in B-lymphoma cells reduced tumor formation. Those tumors that did arise had diminished or extinguished retroviral Fzr. Surprisingly, fzr overexpression dramatically increased B-lymphoma cell susceptibility to natural killer cell (NK) cytotoxicity, a host-resistant mechanism for tumor formation in this model system. These findings implicate fzr as a new category of genes suppressing B-cell tumorigenesis and suggest a novel role for fzr in the target cell interaction with NK cells.


2018 ◽  
Vol 447 (1-2) ◽  
pp. 111-124 ◽  
Author(s):  
Mehdi Najar ◽  
Mohammad Fayyad-Kazan ◽  
Nathalie Meuleman ◽  
Dominique Bron ◽  
Hussein Fayyad-Kazan ◽  
...  

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