Pathways Participating in Activation of Mouse Uterine Natural Killer Cells During Pregnancy1

Abstract Activated natural killer (NK) cells proliferate in large numbers in murine mesometrial endometrium from Day 6 to Day 12 of gestation (term = 19 gestation days) to become the most abundant uterine lymphocytes. Early human decidua contains analogous CD56+/CD16− cells. Murine uterine (u)NK cells localize to decidua basalis and mesometrial lymphoid aggregate of pregnancy (MLAp). Decidua and MLAp are transient, pregnancy-associated tissues traversed by maternal arteries to the placentas. Uterine NK cells sensitize these arteries, facilitating their structural changes into high-volume conduits by Gestation Day 10 through release of interleukin (IL)-18, interferon (IFN)-γ, vascular endothelial growth factor (VEGF), and other molecules. Little information exists concerning where, when, or how murine or human uNK cells become activated. In murine lymphoid tissue, three NK cell adaptor-mediated activation pathways are known: FcRγ/CD3ζ, DNAX-activating protein (DAP) 10, and DAP12 (genes Fcgr3/Cd3z, Hcst, and Tyrobp, respectively). Expression of ligands for these receptors was demonstrated in implantation sites of normal C57BL/6J mice. Then, histological and morphometric analyses of implantation sites in mice with genetic inactivation of each pathway were undertaken. Implantation sites in DAP10−/− (Hcst deleted) mice appeared normal, spiral artery modification occurred, and concentrations of IFN-γ in MLAp and decidua basalis were similar to those in time-matched C57BL/6J. Implantation sites of FcRγ−/−/CD3ζ−/− (Fcgr3/Cd3z double knockout), DAP12 (Tyrobp)-loss-of-function-mutant, and FcRγ−/−/DAP12−/− (Fcgr3/Tyrobp double knockout) mice differentiated abundant but functionally impaired uNK cells that could not modify spiral arteries. These data reveal key importance of FcRγ−/−/CD3ζ−/− and thus maternal IgG during activation of mouse uNK cells and assign DAP12 but not DAP10 signaling contributions.

[1]  J. Trowsdale,et al.  Two Human ULBP/RAET1 Molecules with Transmembrane Regions Are Ligands for NKG2D1 , 2004, The Journal of Immunology.

[2]  J. Kingdom,et al.  Complex patterns of GCM1 mRNA and protein in villous and extravillous trophoblast cells of the human placenta. , 2004, Placenta.

[3]  T. Taniguchi,et al.  Costimulatory signals mediated by the ITAM motif cooperate with RANKL for bone homeostasis , 2004, Nature.

[4]  P. Park,et al.  Human Decidual Natural Killer Cells Are a Unique NK Cell Subset with Immunomodulatory Potential , 2003, The Journal of experimental medicine.

[5]  Luchuan Liang,et al.  Assessment of Requirements for IL-15 and IFN Regulatory Factors in Uterine NK Cell Differentiation and Function During Pregnancy 1 , 2003, The Journal of Immunology.

[6]  S. Akira,et al.  Analysis of Cytokine Regulators Inducing Interferon Production by Mouse Uterine Natural Killer Cells1 , 2003, Biology of reproduction.

[7]  P. Leibson,et al.  NKG2D-DAP10 triggers human NK cell–mediated killing via a Syk-independent regulatory pathway , 2003, Nature Immunology.

[8]  L. Lanier,et al.  NKG2D triggers cytotoxicity in mouse NK cells lacking DAP12 or Syk family kinases , 2003, Nature Immunology.

[9]  P. Joazeiro,et al.  Subset classification of mouse uterine natural killer cells by DBA lectin reactivity. , 2003, Placenta.

[10]  Takashi Saito,et al.  IgE-Mediated Activation of NK Cells Through FcγRIII1 , 2003, The Journal of Immunology.

[11]  N. Umesaki,et al.  Granulated metrial gland cells in the murine uterus: Localization, kinetics, and the functional role in angiogenesis during pregnancy , 2003, Microscopy research and technique.

[12]  M. Colonna,et al.  NKG2D recruits two distinct adapters to trigger NK cell activation and costimulation , 2002, Nature Immunology.

[13]  É. Vivier,et al.  Selective associations with signaling proteins determine stimulatory versus costimulatory activity of NKG2D , 2002, Nature Immunology.

[14]  P. Leibson,et al.  Natural killer cell activation in mice and men: different triggers for similar weapons? , 2002, Nature Immunology.

[15]  L. Lanier,et al.  High levels of RAE-1 isoforms on mouse tumor cell lines assessed by anti-"pan" RAE-1 antibody confer tumor susceptibility to NK cells. , 2002, Biochemical and biophysical research communications.

[16]  N. Maeda,et al.  Contributions from Self-Renewal and Trafficking to the Uterine NK Cell Population of Early Pregnancy1 , 2002, The Journal of Immunology.

[17]  Takashi Saito,et al.  Negative Regulation of Expression and Function of FcγRIII by CD3ζ in Murine NK Cells1 , 2001, The Journal of Immunology.

[18]  L. Lanier,et al.  The ITAM-bearing transmembrane adaptor DAP12 in lymphoid and myeloid cell function. , 2000, Immunology today.

[19]  Jun Wu,et al.  Dap10 and Dap12 Form Distinct, but Functionally Cooperative, Receptor Complexes in Natural Killer Cells , 2000, The Journal of experimental medicine.

[20]  J. Ortaldo,et al.  Combined natural killer cell and dendritic cell functional deficiency in KARAP/DAP12 loss-of-function mutant mice. , 2000, Immunity.

[21]  J. D. Di Santo,et al.  Interferon γ Contributes to Initiation of Uterine Vascular Modification, Decidual Integrity, and Uterine Natural Killer Cell Maturation during Normal Murine Pregnancy , 2000, The Journal of experimental medicine.

[22]  T. Mcclanahan,et al.  Retinoic acid early inducible genes define a ligand family for the activating NKG2D receptor in mice. , 2000, Immunity.

[23]  R. Biassoni,et al.  Identification and Molecular Characterization of Nkp30, a Novel Triggering Receptor Involved in Natural Cytotoxicity Mediated by Human Natural Killer Cells , 1999, The Journal of experimental medicine.

[24]  S. Anderson,et al.  Structure/function relationship of activating Ly-49D and inhibitory Ly-49G2 NK receptors. , 1999, Journal of immunology.

[25]  Michael J. Wilson,et al.  Cutting edge: KAP10, a novel transmembrane adapter protein genetically linked to DAP12 but with unique signaling properties. , 1999, Journal of immunology.

[26]  A. Ashkar,et al.  Interferon-γ Contributes to the Normalcy of Murine Pregnancy , 1999 .

[27]  Jun Wu,et al.  An activating immunoreceptor complex formed by NKG2D and DAP10. , 1999, Science.

[28]  S. Anderson,et al.  Induction of DAP12 phosphorylation, calcium mobilization, and cytokine secretion by Ly49H , 1999, Journal of leukocyte biology.

[29]  R. Biassoni,et al.  Molecular Cloning of NKp46: A Novel Member of the Immunoglobulin Superfamily Involved in Triggering of Natural Cytotoxicity , 1998, The Journal of experimental medicine.

[30]  Kathleen M. Smith,et al.  Ly-49D and Ly-49H associate with mouse DAP12 and form activating receptors. , 1998, Journal of immunology.

[31]  Jun Wu,et al.  Association of DAP12 with activating CD94/NKG2C NK cell receptors. , 1998, Immunity.

[32]  B. Croy,et al.  Engraftment of Bone Marrow from Severe Combined Immunodeficient (SCID) Mice Reverses the Reproductive Deficits in Natural Killer Cell–deficient tgε26 Mice , 1998, The Journal of experimental medicine.

[33]  Seung Yong Park,et al.  Association with FcRγ Is Essential for Activation Signal through NKR-P1 (CD161) in Natural Killer (NK) Cells and NK1.1+ T Cells , 1997, The Journal of experimental medicine.

[34]  C. Story,et al.  Human placental Fc receptors and the transmission of antibodies from mother to fetus. , 1997, Journal of reproductive immunology.

[35]  J. S. Hunt,et al.  Expression of the inducible nitric oxide synthase gene in mouse uterine leukocytes and potential relationships with uterine function during pregnancy. , 1997, Biology of reproduction.

[36]  É. Vivier,et al.  Human killer cell activatory receptors for MHC class I molecules are included in a multimeric complex expressed by natural killer cells. , 1997, Journal of immunology.

[37]  P. Leibson Signal transduction during natural killer cell activation: inside the mind of a killer. , 1997, Immunity.

[38]  S. Anderson,et al.  The Ly-49D Receptor Activates Murine Natural Killer Cells , 1996, The Journal of experimental medicine.

[39]  T. Joh,et al.  Genomic structures and characterization of Rae1 family members encoding GPI-anchored cell surface proteins and expressed predominantly in embryonic mouse brain. , 1996, Journal of biochemistry.

[40]  B. Croy,et al.  Accounting for the peripartum loss of granulated metrial gland cells, a natural killer cell population, from the pregnant mouse uterus , 1996, Journal of leukocyte biology.

[41]  D. Olive,et al.  Binding of phosphatidyl-inositol-3-OH kinase to CD28 is required for T-cell signalling , 1994, Nature.

[42]  L. Cantley,et al.  T-cell antigen CD28 interacts with the lipid kinase phosphatidylinositol 3-kinase by a cytoplasmic Tyr(P)-Met-Xaa-Met motif. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[43]  J. Ravetch,et al.  FcR γ chain deletion results in pleiotrophic effector cell defects , 1994, Cell.

[44]  R. Ueda,et al.  Abnormal T cell development in CD3‐zeta‐/‐ mutant mice and identification of a novel T cell population in the intestine. , 1993, The EMBO journal.

[45]  J. Fox,et al.  Efficacy of tribromoethanol anesthesia in mice. , 1993, Laboratory animal science.

[46]  E. Reinherz,et al.  A population of early fetal thymocytes expressing FcγRII III contains precursors of T lymphocytes and natural killer cells , 1992, Cell.

[47]  J. D. Young,et al.  Mouse granulated metrial gland cells originate by local activation of uterine natural killer lymphocytes. , 1991, Biology of reproduction.

[48]  L. Lanier,et al.  Analysis of Fc gamma RIII (CD16) membrane expression and association with CD3 zeta and Fc epsilon RI-gamma by site-directed mutation. , 1991, Journal of immunology.

[49]  T. Kurosaki,et al.  A single amino acid in the glycosyl phosphatidylinositol attachment domain determines the membrane topology of FcγRIII , 1989, Nature.

[50]  L. Lanier,et al.  Co-association of CD3ζ with a receptor (CD16) for IgG Fc on human natural killer cells , 1989, Nature.

[51]  S. Peel Granulated metrial gland cells. , 1989, Advances in anatomy, embryology, and cell biology.

[52]  M. Monk,et al.  HPRT-deficient (Lesch–Nyhan) mouse embryos derived from germline colonization by cultured cells , 1987, Nature.

[53]  S. Peel,et al.  The structure and differentiation of granulated metrial gland cells of the pregnant mouse uterus , 1977, Cell and Tissue Research.

[54]  A. Ashkar,et al.  Interferon-gamma contributes to the normalcy of murine pregnancy. , 1999, Biology of reproduction.

[55]  Gary A. Boorman,et al.  Pathology of the Mouse: Reference and Atlas , 1999 .