CD169+ macrophages mediate the transport of bacteria to T cell zones by trans-infecting CD8α+ DCs. CD169+ macrophages mediate the transport of bacteria.

Slides:



Advertisements
Similar presentations
High-dimensional analysis of lymphoid CD4+ T cells identified distinct TFH cell subsets in HIV+ patients and HCs. High-dimensional analysis of lymphoid.
Advertisements

Dominant IL-21 expression in TFH cells correlate with B cell pathology in HIV-infected LNs. Dominant IL-21 expression in TFH cells correlate with B cell.
Fibroblast activation in WT and NFATc2-deficient mice.
Splenic CD169+ macrophages trap and prevent early Lm replication and spread. Splenic CD169+ macrophages trap and prevent early Lm replication and spread.
Fluorescence-stained images and respective bright-field images of mouse spleen tissue sections area investigated using Raman spectroscopy. Fluorescence-stained.
Smaller T cell zone FRC areas in aged spleens.
Immunologic responses after the MN-mediated cancer immunotherapy.
FIP200 deficiency alters mitochondria activation and ROS production in T cells. FIP200 deficiency alters mitochondria activation and ROS production in.
Specific depletion of TFH and LCMV-specific CD4 T cells.
CCL21 localizes to T cell zone FRCs in young and aged spleens.
CD8α+ DC-deficient mice are highly susceptible to Lm infection in the absence of CD169+ macrophages. CD8α+ DC-deficient mice are highly susceptible to.
CD169+ macrophages play a critical role in mediating innate immune cell reorganization. CD169+ macrophages play a critical role in mediating innate immune.
Nuclear Arp3 mediates formation of TCR-induced nuclear actin filaments
Specific depletion of CD4-DTR–derived CD4 T cells.
Splenic CD169+ macrophages express a unique gene profile.
The TGF-β pathway is activated in the skin after C
IL-27–eGFP is highly expressed by cDC1 cells and Ly6Chi monocytes after vaccine adjuvant administration. IL-27–eGFP is highly expressed by cDC1 cells and.
Regulatory CD4+ T cell–derived IL-10 is important for B cell differentiation and the GC response. Regulatory CD4+ T cell–derived IL-10 is important for.
CD169+ macrophages mediate Lm translocation to the splenic T cell zones. CD169+ macrophages mediate Lm translocation to the splenic T cell zones. (A) Confocal.
Altered distribution of γδT IELs in GPR55-deficient mice.
Human PBMC-derived MERS-CoV–specific T cells are multifunctional.
Resistance of CD141+ DCs to influenza virus in vivo in humanized mice.
Cytosolic entry of Lm required for CD8α+ DC recruitment.
Virus-specific T cell responses are detected in all MERS survivors.
Resistance of CD141+ DCs to HIV and influenza virus infection at the level of viral fusion. Resistance of CD141+ DCs to HIV and influenza virus infection.
NRP1-expressing myeloid cells influence adipocyte hypertrophy, development of fatty liver, and CLSs. NRP1-expressing myeloid cells influence adipocyte.
Macrophage-resident NRP1 promotes FA uptake.
NRP1-expressing myeloid cells contribute to adipose tissue vascularization. NRP1-expressing myeloid cells contribute to adipose tissue vascularization.
DC subset cooperation for activation of antiviral T cells.
Neutrophil recruitment to the colonic lamina propria depends on CD4+ T cells. Neutrophil recruitment to the colonic lamina propria depends on CD4+ T cells.
T-bethi MP cells produce IFN-γ in response to IL-12.
IL-10R-deficient macrophages secrete IL-23, inducing IL-22 secretion by ILC3 and TH17 cells. IL-10R-deficient macrophages secrete IL-23, inducing IL-22.
Low accessibility to Ag for CTLs leads to low proliferation of effectors. Low accessibility to Ag for CTLs leads to low proliferation of effectors. Intravital.
Immune cell recruitment after the NIR-boosted and MN-mediated cancer immunotherapy. Immune cell recruitment after the NIR-boosted and MN-mediated cancer.
NCMs regulate T cell survival in TLOs via PD-L1.
PD-L1 selectively marks circulating NCMs.
PD-L1 expression is maintained on NCMs under inflammatory conditions and PD-L1+NCMs are found in TLOs. PD-L1 expression is maintained on NCMs under inflammatory.
Fig. 5 Hypoxic tumors from obese mice associate with increased production of IL-6 by adipocytes and myeloid cells. Hypoxic tumors from obese mice associate.
Cell viability tests. Cell viability tests. SEM images of (A) MC3T3-E1 cells and (B) MSCs on days 1, 3, and 5 of culture. (C) Survival rates of MC3T3-E1.
Tumor control by necroptotic cells requires BATF3+cDC1 and CD8+leukocytes. Tumor control by necroptotic cells requires BATF3+cDC1 and CD8+leukocytes. (A)
Fig. 3 Intrarenal and RDLN lymphangiogenesis accompanied by lymphocyte expansion in the kidney, RDLN, and spleen. Intrarenal and RDLN lymphangiogenesis.
BAP1 is required for homeostatic and antigen-driven expansion of peripheral T cells. BAP1 is required for homeostatic and antigen-driven expansion of peripheral.
Fig. 4 Super-resolution live imaging of calcium containing vesicle transports via lysosomes. Super-resolution live imaging of calcium containing vesicle.
RORα deficiency in Tregs results in exaggerated skin inflammation in response to EC sensitization. RORα deficiency in Tregs results in exaggerated skin.
CD25 expression identifies two transcriptionally distinct subsets of very early effector cells. CD25 expression identifies two transcriptionally distinct.
CypD-deficient mice are susceptible to Mtb infection.
CD25 surface expression and TCR signal strength predict T helper differentiation and memory potential of early effector T cells in vivo. CD25 surface expression.
Fig. 1 Neu1−/− fibroblasts have characteristics of myofibroblasts.
S-Affs colocalize with SUMO in mammalian cells.
Type I and III IFNR expression on hematopoietic cells is required for protection against IA. Type I and III IFNR expression on hematopoietic cells is required.
Fig. 3 IRF8 is required for macrophage migration toward the epicenter in the injured spinal cord during the recovery phase. IRF8 is required for macrophage.
AEGIS autonomous targeting process.
IDH3α interacts with cSHMT during S phase at the nuclear lamina
Fig. 2 IRF8 is expressed in CD68+ macrophages after SCI.
Fig. 5. Vascularization of human liver seed grafts.
Fig. 3 Mmp-2−/− mice are protected from obesity and leptin resistance.
Chronic Treg reduction results in dermal fibrosis.
IFN treatment of human midgestation villous explants induces syncytial knot formation. IFN treatment of human midgestation villous explants induces syncytial.
Impact of FRC-specific Myd88 ablation on omental FALC organization.
Fig. 2 RVFV causes pathology within the liver, uterus, and placenta of pregnant dams. RVFV causes pathology within the liver, uterus, and placenta of pregnant.
Fibroblast activation in WT and NFATc2-deficient mice.
Expansion of omental FRCs and FALC remodeling after intraperitoneal exposure to bacterial antigen. Expansion of omental FRCs and FALC remodeling after.
Lin28b promotes the positive selection of CD5+ ImmB cells in neonatal mice. Lin28b promotes the positive selection of CD5+ ImmB cells in neonatal mice.
Acute circadian disruption alters ILC3 cytokine secretion.
REV-ERBα deficiency reduces frequency and number of NKp46+ ILC3s.
Fig. 3 MCA-mediated neutrophil recruitment accelerates bacterial clearance in the skin. MCA-mediated neutrophil recruitment accelerates bacterial clearance.
Ectopic Lin28b functionally replaces CD19 in B cell development and maintenance. Ectopic Lin28b functionally replaces CD19 in B cell development and maintenance.
Meningeal γδ T cells are biased toward IL-17 production.
Fetal-derived γδ T cells infiltrate the meninges from birth.
The neuropod cells. The neuropod cells. (Top left) Neuropod cells synapse with sensory neurons in the small intestine, as shown in a confocal microscopy.
Presentation transcript:

CD169+ macrophages mediate the transport of bacteria to T cell zones by trans-infecting CD8α+ DCs. CD169+ macrophages mediate the transport of bacteria to T cell zones by trans-infecting CD8α+ DCs. (A) Confocal images of spleen sections from WT or CD169-DTR mice at 6 hpi. Colocalization of CD11c and CD8α is shown in white. Lm are rendered with spots in green. White arrowheads indicate Lm in the MZ. Scale bars, 70 to 80 μm. (B) Confocal images of spleen sections from WT or CD169-DTR mice at 9 hpi. Spleen sections stained for Lm (green), CD169 (blue), and CD11c (red). Colocalization of CD11c and CD8α is shown in white. Lm are rendered with spots. White arrows indicate areas of Lm. Scale bars, 30 μm. (C) High-magnification confocal image showing Lm-infected CD169+ macrophages and CD8α+ DCs in close contact at 3 hpi. Spleen sections stained for Lm (green), CD169 (blue), CD11c (red), and CD8α (light blue). Scale bars, 20 μm. (D and E) Quantification of viable Lm recovered from FACS-sorted myeloid cells from pooled WT or CD169-DTR mice at (D) 1 hpi and (E) 3 hpi (n = 2 to 4). (F) General gating strategy used for CD169+ macrophages and DC subset identification from the spleen. (G) Representative confocal image of WT mice at 3 hpi. Spleen sections stained for Lm (white), CD169 (blue), and CD11c (red). Lm are rendered with spots. White and green arrowheads indicate Lm in CD169+ cells and CD169+CD11c+ cells, respectively. Scale bars, 20 μm. All data are representative of three to four separate experiments with two to four mice per group. Oriana A. Perez et al. Sci. Immunol. 2017;2:eaah5520 Copyright © 2017 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works