TY - JOUR
T1 - NK-cell receptors NKp46 and NCR1 control human metapneumovirus infection
AU - Diab, Mohammad
AU - Glasner, Ariella
AU - Isaacson, Batya
AU - Bar-On, Yotam
AU - Drori, Yaron
AU - Yamin, Rachel
AU - Duev-Cohen, Alexandra
AU - Danziger, Oded
AU - Zamostiano, Rachel
AU - Mandelboim, Michal
AU - Jonjic, Stipan
AU - Bacharach, Eran
AU - Mandelboim, Ofer
N1 - Publisher Copyright:
© 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2017/4/1
Y1 - 2017/4/1
N2 - Natural killer (NK) cells are capable of killing various pathogens upon stimulation of activating receptors. Human metapneumovirus (HMPV) is a respiratory virus, which was discovered in 2001 and is responsible for acute respiratory tract infection in infants and children worldwide. HMPV infection is very common, infecting around 70% of all children under the age of five. Under immune suppressive conditions, HMPV infection can be fatal. Not much is known on how NK cells respond to HMPV. In this study, using reporter assays and NK-cell cytotoxicity assays performed with human and mouse NK cells, we demonstrated that the NKp46-activating receptor and its mouse orthologue Ncr1, both members of the natural cytotoxicity receptor (NCR) family, recognized an unknown ligand expressed by HMPV-infected human cells. We demonstrated that MHC class I is upregulated and MICA is downregulated upon HMPV infection. We also characterized mouse NK-cell phenotype in the blood and the lungs of HMPV-infected mice and found that lung NK cells are more activated and expressing NKG2D, CD43, CD27, KLRG1, and CD69 compared to blood NK cells regardless of HMPV infection. Finally, we demonstrated, using Ncr1-deficient mice, that NCR1 plays a critical role in controlling HMPV infection.
AB - Natural killer (NK) cells are capable of killing various pathogens upon stimulation of activating receptors. Human metapneumovirus (HMPV) is a respiratory virus, which was discovered in 2001 and is responsible for acute respiratory tract infection in infants and children worldwide. HMPV infection is very common, infecting around 70% of all children under the age of five. Under immune suppressive conditions, HMPV infection can be fatal. Not much is known on how NK cells respond to HMPV. In this study, using reporter assays and NK-cell cytotoxicity assays performed with human and mouse NK cells, we demonstrated that the NKp46-activating receptor and its mouse orthologue Ncr1, both members of the natural cytotoxicity receptor (NCR) family, recognized an unknown ligand expressed by HMPV-infected human cells. We demonstrated that MHC class I is upregulated and MICA is downregulated upon HMPV infection. We also characterized mouse NK-cell phenotype in the blood and the lungs of HMPV-infected mice and found that lung NK cells are more activated and expressing NKG2D, CD43, CD27, KLRG1, and CD69 compared to blood NK cells regardless of HMPV infection. Finally, we demonstrated, using Ncr1-deficient mice, that NCR1 plays a critical role in controlling HMPV infection.
KW - HMPV
KW - MHC class I
KW - MICA
KW - NCR1
KW - NCRs
KW - NK cells
KW - NKG2D
KW - NKp46
KW - respiratory infection
UR - http://www.scopus.com/inward/record.url?scp=85014697327&partnerID=8YFLogxK
U2 - 10.1002/eji.201646756
DO - 10.1002/eji.201646756
M3 - Article
C2 - 28191644
AN - SCOPUS:85014697327
SN - 0014-2980
VL - 47
SP - 692
EP - 703
JO - European Journal of Immunology
JF - European Journal of Immunology
IS - 4
ER -