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  1. Article ; Online: Deleting interleukin-10 from myeloid cells exacerbates atherosclerosis in Apoe−/− mice

    Orecchioni, Marco / Wolf, Dennis / Suryawanshi, Vasantika / Winkels, Holger / Kobiyama, Kouji / Makings, Jeffrey / Kiosses, William B. / Ley, Klaus

    Cell. Mol. Life Sci.. 2023 Jan., v. 80, no. 1 p.10-10

    2023  

    Abstract: Atherosclerosis is initiated by subendothelial retention of lipoproteins and cholesterol, which triggers a non-resolving inflammatory process that over time leads to plaque progression in the artery wall. Myeloid cells and in particular macrophages are ... ...

    Abstract Atherosclerosis is initiated by subendothelial retention of lipoproteins and cholesterol, which triggers a non-resolving inflammatory process that over time leads to plaque progression in the artery wall. Myeloid cells and in particular macrophages are the primary drivers of the inflammatory response and plaque formation. Several immune cells including macrophages, T cells and B cells secrete the anti-inflammatory cytokine IL-10, known to be essential for the atherosclerosis protection. The cellular source of IL-10 in natural atherosclerosis progression is unknown. This study aimed to determine the main IL10-producing cell type in atherosclerosis. To do so, we crossed VertX mice, in which IRES-green fluorescent protein (eGFP) was placed downstream of exon 5 of the Il10 gene, with atherosclerosis-prone Apoe⁻/⁻ mice. We found that myeloid cells express high levels of IL-10 in VertX Apoe⁻/⁻ mice in both chow and western-diet fed mice. By single cell RNA sequencing and flow cytometry analysis, we identified resident and inflammatory macrophages in atherosclerotic plaques as the main IL-10 producers. To address whether IL-10 secreted by myeloid cells is essential for the protection, we utilized LyzMCʳᵉ⁺Il10ᶠˡ/ᶠˡ mice crossed into the Apoe⁻/⁻ background and confirmed that macrophages were unable to secrete IL-10. Chow and western diet-fed LyzMCʳᵉ⁺Il10ᶠˡ/ᶠˡ Apoe⁻/⁻ mice developed significantly larger atherosclerotic plaques as measured by en face morphometry than LyzMCʳᵉ⁻Il10 ᶠˡ/ᶠˡApoe⁻/⁻. Flow cytometry and cytokine measurements suggest that the depletion of IL-10 in myeloid cells increases Th17 cells with elevated CCL2, and TNFα in blood plasma. We conclude that macrophage-derived IL-10 is critical for limiting atherosclerosis in mice.
    Keywords RNA ; Western diets ; atherosclerosis ; blood plasma ; cholesterol ; exons ; flow cytometry ; fluorescent proteins ; inflammation ; interleukin-10 ; lipoproteins ; macrophages ; morphometry
    Language English
    Dates of publication 2023-01
    Size p. 10.
    Publishing place Springer International Publishing
    Document type Article ; Online
    ZDB-ID 1358415-7
    ISSN 1420-9071 ; 1420-682X
    ISSN (online) 1420-9071
    ISSN 1420-682X
    DOI 10.1007/s00018-022-04649-9
    Database NAL-Catalogue (AGRICOLA)

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  2. Article ; Online: Intratumoral Cancer Cell Intravasation Can Occur Independent of Invasion into the Adjacent Stroma.

    Deryugina, Elena I / Kiosses, William B

    Cell reports

    2017  Volume 19, Issue 3, Page(s) 601–616

    Abstract: Intravasation, active entry of cancer cells into the circulation, is often considered to be a relatively late event in tumor development occurring after stromal invasion. Here, we provide evidence that intravasation can be initiated early during tumor ... ...

    Abstract Intravasation, active entry of cancer cells into the circulation, is often considered to be a relatively late event in tumor development occurring after stromal invasion. Here, we provide evidence that intravasation can be initiated early during tumor development and proceed in parallel to or independent of tumor invasion into surrounding stroma. By applying direct and unbiased intravasation-scoring methods to two histologically distinct human cancer types in live-animal models, we demonstrate that intravasation takes place almost exclusively within the tumor core, involves intratumoral vasculature, and does not involve vasculotropic cancer cells invading tumor-adjacent stroma and migrating along tumor-converging blood vessels. Highlighting an additional role for EGFR in cancer, we find that EGFR is required for the development of an intravasation-sustaining intratumoral vasculature. Intratumoral localization of intravasation supports the notion that overt metastases in cancer patients could be initiated much earlier during cancer progression than appreciated within conventional clinical tumor staging systems.
    MeSH term(s) Animals ; Cell Line, Tumor ; Cell Movement ; Chick Embryo ; Disease Models, Animal ; Ear/pathology ; Green Fluorescent Proteins/metabolism ; Humans ; Hypoxia/pathology ; Mice, Inbred C57BL ; Mice, Inbred NOD ; Mice, SCID ; Neoplasm Invasiveness ; Neoplasm Metastasis ; Neoplasms/pathology ; Neovascularization, Pathologic ; Permeability ; Receptor, Epidermal Growth Factor/metabolism ; Stromal Cells/pathology
    Chemical Substances Green Fluorescent Proteins (147336-22-9) ; Receptor, Epidermal Growth Factor (EC 2.7.10.1)
    Language English
    Publishing date 2017-04-18
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2649101-1
    ISSN 2211-1247 ; 2211-1247
    ISSN (online) 2211-1247
    ISSN 2211-1247
    DOI 10.1016/j.celrep.2017.03.064
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Super-Resolution Microscopy and Particle-Tracking Approaches for the Study of Vesicular Trafficking in Primary Neutrophils.

    Johnson, Jennifer L / Pestonjamasp, Kersi / Kiosses, William B / Catz, Sergio D

    Methods in molecular biology (Clifton, N.J.)

    2020  Volume 2233, Page(s) 193–202

    Abstract: Neutrophils are short-lived cells after isolation. The analysis of neutrophil vesicular trafficking requires rapid and gentle handling. Recently developed super-resolution microscopy technologies have generated unparalleled opportunities to help ... ...

    Abstract Neutrophils are short-lived cells after isolation. The analysis of neutrophil vesicular trafficking requires rapid and gentle handling. Recently developed super-resolution microscopy technologies have generated unparalleled opportunities to help understand the molecular mechanisms regulating neutrophil vesicular trafficking, exocytosis, and associated functions at the molecular level. Here, we describe super-resolution and total internal reflection fluorescence (TIRF) microscopy approaches for the analysis of vesicular trafficking and associated functions of primary neutrophils.
    MeSH term(s) Cell Movement/genetics ; Exocytosis/genetics ; Humans ; Microscopy, Fluorescence/methods ; Neutrophils/metabolism ; Neutrophils/ultrastructure ; Primary Cell Culture/methods ; Protein Transport/genetics ; rab GTP-Binding Proteins/genetics
    Chemical Substances rab GTP-Binding Proteins (EC 3.6.5.2)
    Language English
    Publishing date 2020-09-30
    Publishing country United States
    Document type Journal Article
    ISSN 1940-6029
    ISSN (online) 1940-6029
    DOI 10.1007/978-1-0716-1044-2_13
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Deleting interleukin-10 from myeloid cells exacerbates atherosclerosis in Apoe

    Orecchioni, Marco / Wolf, Dennis / Suryawanshi, Vasantika / Winkels, Holger / Kobiyama, Kouji / Makings, Jeffrey / Kiosses, William B / Ley, Klaus

    Cellular and molecular life sciences : CMLS

    2022  Volume 80, Issue 1, Page(s) 10

    Abstract: Atherosclerosis is initiated by subendothelial retention of lipoproteins and cholesterol, which triggers a non-resolving inflammatory process that over time leads to plaque progression in the artery wall. Myeloid cells and in particular macrophages are ... ...

    Abstract Atherosclerosis is initiated by subendothelial retention of lipoproteins and cholesterol, which triggers a non-resolving inflammatory process that over time leads to plaque progression in the artery wall. Myeloid cells and in particular macrophages are the primary drivers of the inflammatory response and plaque formation. Several immune cells including macrophages, T cells and B cells secrete the anti-inflammatory cytokine IL-10, known to be essential for the atherosclerosis protection. The cellular source of IL-10 in natural atherosclerosis progression is unknown. This study aimed to determine the main IL10-producing cell type in atherosclerosis. To do so, we crossed VertX mice, in which IRES-green fluorescent protein (eGFP) was placed downstream of exon 5 of the Il10 gene, with atherosclerosis-prone Apoe
    MeSH term(s) Animals ; Mice ; Atherosclerosis/genetics ; Atherosclerosis/metabolism ; Cytokines/metabolism ; Disease Models, Animal ; Interleukin-10/genetics ; Interleukin-10/metabolism ; Macrophages/metabolism ; Mice, Inbred C57BL ; Plaque, Atherosclerotic/metabolism ; Mice, Knockout, ApoE
    Chemical Substances Cytokines ; Interleukin-10 (130068-27-8) ; IL10 protein, mouse
    Language English
    Publishing date 2022-12-10
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 1358415-7
    ISSN 1420-9071 ; 1420-682X
    ISSN (online) 1420-9071
    ISSN 1420-682X
    DOI 10.1007/s00018-022-04649-9
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Clustering of phosphatase RPTPα promotes Src signaling and the arthritogenic action of synovial fibroblasts.

    Sendo, Sho / Kiosses, William B / Yang, Shen / Wu, Dennis J / Lee, Daniel W K / Liu, Lin / Aschner, Yael / Vela, Allison J / Downey, Gregory P / Santelli, Eugenio / Bottini, Nunzio

    Science signaling

    2023  Volume 16, Issue 792, Page(s) eabn8668

    Abstract: Receptor-type protein phosphatase α (RPTPα) promotes fibroblast-dependent arthritis and fibrosis, in part, by enhancing the activation of the kinase SRC. Synovial fibroblasts lining joint tissue mediate inflammation and tissue damage, and their ... ...

    Abstract Receptor-type protein phosphatase α (RPTPα) promotes fibroblast-dependent arthritis and fibrosis, in part, by enhancing the activation of the kinase SRC. Synovial fibroblasts lining joint tissue mediate inflammation and tissue damage, and their infiltration into adjacent tissues promotes disease progression. RPTPα includes an ectodomain and two intracellular catalytic domains (D1 and D2) and, in cancer cells, undergoes inhibitory homodimerization, which is dependent on a D1 wedge motif. Through single-molecule localization and labeled molecule interaction microscopy of migrating synovial fibroblasts, we investigated the role of RPTPα dimerization in the activation of SRC, the migration of synovial fibroblasts, and joint damage in a mouse model of arthritis. RPTPα clustered with other RPTPα and with SRC molecules in the context of actin-rich structures. A known dimerization-impairing mutation in the wedge motif (P210L/P211L) and the deletion of the D2 domain reduced RPTPα-RPTPα clustering; however, it also unexpectedly reduced RPTPα-SRC association. The same mutations also reduced recruitment of RPTPα to actin-rich structures and inhibited SRC activation and cellular migration. An antibody against the RPTPα ectodomain that prevented the clustering of RPTPα also inhibited RPTPα-SRC association and SRC activation and attenuated fibroblast migration and joint damage in arthritic mice. A catalytically inactivating RPTPα-C469S mutation protected mice from arthritis and reduced SRC activation in synovial fibroblasts. We conclude that RPTPα clustering retains it to actin-rich structures to promote SRC-mediated fibroblast migration and can be modulated through the extracellular domain.
    MeSH term(s) Animals ; Mice ; Actins ; Arthritis ; Cluster Analysis ; Fibroblasts/metabolism ; Phosphoprotein Phosphatases ; Protein Tyrosine Phosphatases/metabolism ; Receptor-Like Protein Tyrosine Phosphatases, Class 4/genetics ; Receptor-Like Protein Tyrosine Phosphatases, Class 4/metabolism
    Chemical Substances Actins ; Phosphoprotein Phosphatases (EC 3.1.3.16) ; Protein Tyrosine Phosphatases (EC 3.1.3.48) ; Receptor-Like Protein Tyrosine Phosphatases, Class 4 (EC 3.1.3.48) ; Ptpra protein, mouse (EC 3.1.3.48)
    Language English
    Publishing date 2023-07-04
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2417226-1
    ISSN 1937-9145 ; 1945-0877
    ISSN (online) 1937-9145
    ISSN 1945-0877
    DOI 10.1126/scisignal.abn8668
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Nonclassical monocytes potentiate anti-tumoral CD8

    Padgett, Lindsey E / Marcovecchio, Paola M / Olingy, Claire E / Araujo, Daniel J / Steel, Kathleen / Dinh, Huy Q / Alimadadi, Ahmad / Zhu, Yanfang Peipei / Meyer, Melissa A / Kiosses, William B / Thomas, Graham D / Hedrick, Catherine C

    Frontiers in immunology

    2023  Volume 14, Page(s) 1101497

    Abstract: ... ...

    Abstract CD8
    MeSH term(s) Mice ; Animals ; Monocytes ; CD8-Positive T-Lymphocytes ; Endothelial Cells ; Lung ; Neoplasms/metabolism ; Tumor Microenvironment
    Language English
    Publishing date 2023-06-22
    Publishing country Switzerland
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2606827-8
    ISSN 1664-3224 ; 1664-3224
    ISSN (online) 1664-3224
    ISSN 1664-3224
    DOI 10.3389/fimmu.2023.1101497
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: HLA class I hyper-expression unmasks beta cells but not alpha cells to the immune system in pre-diabetes.

    Benkahla, Mehdi A / Sabouri, Somayeh / Kiosses, William B / Rajendran, Sakthi / Quesada-Masachs, Estefania / von Herrath, Matthias G

    Journal of autoimmunity

    2021  Volume 119, Page(s) 102628

    Abstract: Human leukocyte antigens of class-I (HLA-I) molecules are hyper-expressed in insulin-containing islets (ICI) of type 1 diabetic (T1D) donors. This study investigated the HLA-I expression in autoantibody positive (AAB+) donors and defined its intra-islet ... ...

    Abstract Human leukocyte antigens of class-I (HLA-I) molecules are hyper-expressed in insulin-containing islets (ICI) of type 1 diabetic (T1D) donors. This study investigated the HLA-I expression in autoantibody positive (AAB+) donors and defined its intra-islet and intracellular localization as well as proximity to infiltrating CD8 T cells with high-resolution confocal microscopy. We found HLA-I hyper-expression had already occurred prior to clinical diagnosis of T1D in islets of AAB+ donors. Interestingly, throughout all stages of disease, HLA-I was mostly expressed by alpha cells. Hyper-expression in AAB+ and T1D donors was associated with intra-cellular accumulation in the Golgi. Proximity analysis showed a moderate but significant correlation between HLA-I and infiltrating CD8 T cells only in ICI of T1D donors, but not in AAB+ donors. These observations not only demonstrate a very early, islet-intrinsic immune-independent increase of HLA-I during diabetes pathogenesis, but also point towards a role for alpha cells in T1D.
    MeSH term(s) Autoantibodies/immunology ; Autoantigens/immunology ; Autoimmunity ; Biomarkers ; Diabetes Mellitus, Type 1/etiology ; Diabetes Mellitus, Type 1/metabolism ; Disease Susceptibility/immunology ; Fluorescent Antibody Technique ; Gene Expression ; Glucagon-Secreting Cells/metabolism ; Histocompatibility Antigens Class I/genetics ; Histocompatibility Antigens Class I/immunology ; Humans ; Insulin-Secreting Cells/immunology ; Insulin-Secreting Cells/metabolism ; Islets of Langerhans/immunology ; Islets of Langerhans/metabolism ; Islets of Langerhans/pathology ; Prediabetic State/etiology ; Prediabetic State/immunology ; Protein Transport ; T-Lymphocyte Subsets/immunology ; T-Lymphocyte Subsets/metabolism
    Chemical Substances Autoantibodies ; Autoantigens ; Biomarkers ; Histocompatibility Antigens Class I
    Language English
    Publishing date 2021-03-09
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 639452-8
    ISSN 1095-9157 ; 0896-8411
    ISSN (online) 1095-9157
    ISSN 0896-8411
    DOI 10.1016/j.jaut.2021.102628
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Human CD79b

    Meyer, Melissa A / Dinh, Huy Q / Alimadadi, Ahmad / Araujo, Daniel J / Chatterjee, Nandini / Gutierrez, Norma A / Zhu, Yanfang Peipei / Hunter, Emma L / Liang, Shu / Seumois, Gregory / Kiosses, William B / Catz, Sergio D / Vijayanand, Pandurangan / Ottensmeier, Christian / Hedrick, Catherine C

    Frontiers in immunology

    2023  Volume 14, Page(s) 1224045

    Abstract: Purpose: Due to their abundance in the blood, low RNA content, and short lifespan, neutrophils have been classically considered to be one homogenous pool. However, recent work has found that mature neutrophils and neutrophil progenitors are composed of ... ...

    Abstract Purpose: Due to their abundance in the blood, low RNA content, and short lifespan, neutrophils have been classically considered to be one homogenous pool. However, recent work has found that mature neutrophils and neutrophil progenitors are composed of unique subsets exhibiting context-dependent functions. In this study, we ask if neutrophil heterogeneity is associated with melanoma incidence and/or disease stage.
    Experimental design: Using mass cytometry, we profiled melanoma patient blood for unique cell surface markers among neutrophils. Markers were tested for their predictiveness using flow cytometry data and random forest machine learning.
    Results: We identified CD79b
    Conclusion: Our work suggests that CD79b
    MeSH term(s) Humans ; Neutrophils ; Antigens, CD19 ; B-Lymphocytes ; Leukemia, Lymphocytic, Chronic, B-Cell ; Melanoma
    Chemical Substances Antigens, CD19
    Language English
    Publishing date 2023-10-31
    Publishing country Switzerland
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2606827-8
    ISSN 1664-3224 ; 1664-3224
    ISSN (online) 1664-3224
    ISSN 1664-3224
    DOI 10.3389/fimmu.2023.1224045
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: A humanized β

    Wen, Lai / Marki, Alex / Wang, Zhihao / Orecchioni, Marco / Makings, Jeffrey / Billitti, Monica / Wang, Erpei / Suthahar, Sujit S A / Kim, Kenneth / Kiosses, William B / Mikulski, Zbigniew / Ley, Klaus

    Cell reports

    2022  Volume 39, Issue 9, Page(s) 110876

    Abstract: ... ...

    Abstract β
    MeSH term(s) Animals ; CD18 Antigens/genetics ; Cell Adhesion ; Cell Adhesion Molecules ; Integrins ; Mice ; Neutrophil Activation ; Neutrophils
    Chemical Substances CD18 Antigens ; Cell Adhesion Molecules ; Integrins
    Language English
    Publishing date 2022-05-12
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, N.I.H., Extramural
    ZDB-ID 2649101-1
    ISSN 2211-1247 ; 2211-1247
    ISSN (online) 2211-1247
    ISSN 2211-1247
    DOI 10.1016/j.celrep.2022.110876
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: The solute carrier SLC15A4 is required for optimal trafficking of nucleic acid-sensing TLRs and ligands to endolysosomes.

    Rimann, Ivo / Gonzalez-Quintial, Rosana / Baccala, Roberto / Kiosses, William B / Teijaro, John R / Parker, Christopher G / Li, Xiaohong / Beutler, Bruce / Kono, Dwight H / Theofilopoulos, Argyrios N

    Proceedings of the National Academy of Sciences of the United States of America

    2022  Volume 119, Issue 14, Page(s) e2200544119

    Abstract: A function-impairing mutation (feeble) or genomic deletion of SLC15A4 abolishes responses of nucleic acid–sensing endosomal toll-like receptors (TLRs) and significantly reduces disease in mouse models of lupus. Here, we demonstrate disease reduction in ... ...

    Abstract A function-impairing mutation (feeble) or genomic deletion of SLC15A4 abolishes responses of nucleic acid–sensing endosomal toll-like receptors (TLRs) and significantly reduces disease in mouse models of lupus. Here, we demonstrate disease reduction in homozygous and even heterozygous Slc15a4 feeble mutant BXSB male mice with a Tlr7 gene duplication. In contrast to SLC15A4, a function-impairing mutation of SLC15A3 did not diminish type I interferon (IFN-I) production by TLR-activated plasmacytoid dendritic cells (pDCs), indicating divergence of function between these homologous SLC15 family members. Trafficking to endolysosomes and function of SLC15A4 were dependent on the Adaptor protein 3 (AP-3) complex. Importantly, SLC15A4 was required for trafficking and colocalization of nucleic acid–sensing TLRs and their ligands to endolysosomes and the formation of the LAMP2+VAMP3+ hybrid compartment in which IFN-I production is initiated. Collectively, these findings define mechanistic processes by which SLC15A4 controls endosomal TLR function and suggest that pharmacologic intervention to curtail the function of this transporter may be a means to treat lupus and other endosomal TLR-dependent diseases.
    MeSH term(s) Animals ; Endosomes/metabolism ; Ligands ; Lysosomes/metabolism ; Membrane Transport Proteins/genetics ; Mice ; Nucleic Acids ; Toll-Like Receptors/metabolism
    Chemical Substances Ligands ; Membrane Transport Proteins ; Nucleic Acids ; Slc15a4 protein, mouse ; Toll-Like Receptors
    Language English
    Publishing date 2022-03-29
    Publishing country United States
    Document type Journal Article
    ZDB-ID 209104-5
    ISSN 1091-6490 ; 0027-8424
    ISSN (online) 1091-6490
    ISSN 0027-8424
    DOI 10.1073/pnas.2200544119
    Database MEDical Literature Analysis and Retrieval System OnLINE

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