TY - JOUR
T1 - Pregnancy trained decidual NK cells protect pregnancies from harmful Fusobacterium nucleatum infection
AU - Kotzur, Rebecca
AU - Kahlon, Shira
AU - Isaacson, Batya
AU - Gamliel, Moriya
AU - Charpak-Amikam, Yoav
AU - Lieberman, Judy
AU - Bachrach, Gilad
AU - Goldman-Wohl, Debra
AU - Yagel, Simcha
AU - Beharier, Ofer
AU - Mandelboim, Ofer
N1 - Publisher Copyright:
Copyright: © 2024 Kotzur et al.
PY - 2024/1/1
Y1 - 2024/1/1
N2 - Natural killer cells (NKs) found during pregnancy at the maternal-fetal interface named decidual (d)NKs, show signs of education following first pregnancy, resulting in better placentation and fetus-growth, hence termed pregnancy trained dNKs (PTdNKs). Here we show that PTdNKs provide increased protection of the fetus from Fusobacterium nucleatum (FN) infection. We demonstrate that PTdNKs secrete elevated amounts of the bacteriocidal protein granulysin (GNLY) upon incubation with FN compared to dNKs derived from first pregnancies, which leads to increased killing of FN. Furthermore, we showed mechanistically that the GNLY secretion is mediated through the interaction of the FN’s Fap2 protein with Gal-GalNAc present on PTdNKs. Finally, we show in vivo, using GNLY-tg mice that enhanced protection of the fetuses from FN infection is observed, as compared to wild type and that this enhance protection is NK cell dependent. Altogether, we show a new function for PTdNKs as protectors of the fetus from bacterial infection.
AB - Natural killer cells (NKs) found during pregnancy at the maternal-fetal interface named decidual (d)NKs, show signs of education following first pregnancy, resulting in better placentation and fetus-growth, hence termed pregnancy trained dNKs (PTdNKs). Here we show that PTdNKs provide increased protection of the fetus from Fusobacterium nucleatum (FN) infection. We demonstrate that PTdNKs secrete elevated amounts of the bacteriocidal protein granulysin (GNLY) upon incubation with FN compared to dNKs derived from first pregnancies, which leads to increased killing of FN. Furthermore, we showed mechanistically that the GNLY secretion is mediated through the interaction of the FN’s Fap2 protein with Gal-GalNAc present on PTdNKs. Finally, we show in vivo, using GNLY-tg mice that enhanced protection of the fetuses from FN infection is observed, as compared to wild type and that this enhance protection is NK cell dependent. Altogether, we show a new function for PTdNKs as protectors of the fetus from bacterial infection.
UR - http://www.scopus.com/inward/record.url?scp=85182556474&partnerID=8YFLogxK
U2 - 10.1371/journal.ppat.1011923
DO - 10.1371/journal.ppat.1011923
M3 - Article
C2 - 38215172
AN - SCOPUS:85182556474
SN - 1553-7366
VL - 20
JO - PLoS Pathogens
JF - PLoS Pathogens
IS - 1
M1 - e1011923
ER -