TY - JOUR
T1 - The bone marrow is patrolled by NK cells that are primed and expand in response to systemic viral activation
AU - Milo, Idan
AU - Blecher-Gonen, Ronnie
AU - Barnett-Itzhaki, Zohar
AU - Bar-Ziv, Raz
AU - Tal, Orna
AU - Gurevich, Irina
AU - Feferman, Tali
AU - Drexler, Ingo
AU - Amit, Ido
AU - Bousso, Philippe
AU - Shakhar, Guy
N1 - Publisher Copyright: © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2018/7
Y1 - 2018/7
N2 - The bone marrow hosts NK cells whose distribution, motility and response to systemic immune challenge are poorly understood. At steady state, two-photon microscopy of the bone marrow in Ncr1(gfp/+) mice captured motile NK cells interacting with dendritic cells. NK cells expressed markers and effector molecules of mature cells. Following poly (I:C) injection, RNA-Seq of NK cells revealed three phases of transcription featuring immune response genes followed by posttranscriptional processes and proliferation. Functionally, poly (I:C) promoted upregulation of granzyme B, enhanced cytotoxicity in vitro and in vivo, and, in the same individual cells, triggered proliferation. Two-photon imaging revealed that the proportion of sinusoidal NK cells decreased, while at the same time parenchymal NK cells accelerated, swelled and divided within the bone marrow. MVA viremia induced similar responses. Our findings demonstrate that the bone marrow is patrolled by mature NK cells that rapidly proliferate in response to systemic viral challenge while maintaining their effector functions.
AB - The bone marrow hosts NK cells whose distribution, motility and response to systemic immune challenge are poorly understood. At steady state, two-photon microscopy of the bone marrow in Ncr1(gfp/+) mice captured motile NK cells interacting with dendritic cells. NK cells expressed markers and effector molecules of mature cells. Following poly (I:C) injection, RNA-Seq of NK cells revealed three phases of transcription featuring immune response genes followed by posttranscriptional processes and proliferation. Functionally, poly (I:C) promoted upregulation of granzyme B, enhanced cytotoxicity in vitro and in vivo, and, in the same individual cells, triggered proliferation. Two-photon imaging revealed that the proportion of sinusoidal NK cells decreased, while at the same time parenchymal NK cells accelerated, swelled and divided within the bone marrow. MVA viremia induced similar responses. Our findings demonstrate that the bone marrow is patrolled by mature NK cells that rapidly proliferate in response to systemic viral challenge while maintaining their effector functions.
KW - Bone marrow
KW - Cell migration
KW - Cellular proliferation
KW - NK cells
KW - Two-photon imaging
UR - http://www.scopus.com/inward/record.url?scp=85049506786&partnerID=8YFLogxK
U2 - https://doi.org/10.1002/eji.201747378
DO - https://doi.org/10.1002/eji.201747378
M3 - مقالة
C2 - 29624673
SN - 0014-2980
VL - 48
SP - 1137
EP - 1152
JO - European Journal of Immunology
JF - European Journal of Immunology
IS - 7
ER -