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  1. Article ; Online: Migration of myeloid cells during inflammation is differentially regulated by the cell surface receptors Slamf1 and Slamf8.

    Wang, Guoxing / van Driel, Boaz J / Liao, Gongxian / O'Keeffe, Michael S / Halibozek, Peter J / Flipse, Jacky / Yigit, Burcu / Azcutia, Veronica / Luscinskas, Francis W / Wang, Ninghai / Terhorst, Cox

    PloS one

    2015  Volume 10, Issue 3, Page(s) e0121968

    Abstract: ... migration. We conclude that Slamf1 and Slamf8 govern ROS-dependent innate immune responses of myeloid cells ... macrophages and neutrophils is accelerated. These opposing effects of Slamf1 and Slamf8 are cell-intrinsic ... Previous studies have demonstrated that the cell surface receptor Slamf1 (CD150) is requisite ...

    Abstract Previous studies have demonstrated that the cell surface receptor Slamf1 (CD150) is requisite for optimal NADPH-oxidase (Nox2) dependent reactive oxygen species (ROS) production by phagocytes in response to Gram- bacteria. By contrast, Slamf8 (CD353) is a negative regulator of ROS in response to Gram+ and Gram- bacteria. Employing in vivo migration after skin sensitization, induction of peritonitis, and repopulation of the small intestine demonstrates that in vivo migration of Slamf1-/- dendritic cells and macrophages is reduced, as compared to wt mice. By contrast, in vivo migration of Slamf8-/- dendritic cells, macrophages and neutrophils is accelerated. These opposing effects of Slamf1 and Slamf8 are cell-intrinsic as judged by in vitro migration in transwell chambers in response to CCL19, CCL21 or CSF-1. Importantly, inhibiting ROS production of Slamf8-/- macrophages by diphenyleneiodonium chloride blocks this in vitro migration. We conclude that Slamf1 and Slamf8 govern ROS-dependent innate immune responses of myeloid cells, thus modulating migration of these cells during inflammation in an opposing manner.
    MeSH term(s) Animals ; Antigens, CD/genetics ; Antigens, CD/metabolism ; Antigens, CD/physiology ; Cell Movement/genetics ; Cell Movement/physiology ; Chemotaxis/drug effects ; Dendritic Cells/cytology ; Dendritic Cells/metabolism ; Macrophages/cytology ; Macrophages/metabolism ; Membrane Proteins ; Mice ; Mice, Inbred BALB C ; Myeloid Cells/cytology ; Myeloid Cells/metabolism ; Neutrophils/cytology ; Neutrophils/metabolism ; Peritonitis/metabolism ; Peritonitis/pathology ; Reactive Oxygen Species/metabolism ; Receptors, Cell Surface/genetics ; Receptors, Cell Surface/metabolism ; Receptors, Cell Surface/physiology ; Signaling Lymphocytic Activation Molecule Family Member 1
    Chemical Substances Antigens, CD ; Membrane Proteins ; Reactive Oxygen Species ; Receptors, Cell Surface ; SLAM family member 8 protein, mouse ; Slamf1 protein, mouse ; Signaling Lymphocytic Activation Molecule Family Member 1 (169535-43-7)
    Language English
    Publishing date 2015-03-23
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ISSN 1932-6203
    ISSN (online) 1932-6203
    DOI 10.1371/journal.pone.0121968
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Migration of myeloid cells during inflammation is differentially regulated by the cell surface receptors Slamf1 and Slamf8.

    Guoxing Wang / Boaz J van Driel / Gongxian Liao / Michael S O'Keeffe / Peter J Halibozek / Jacky Flipse / Burcu Yigit / Veronica Azcutia / Francis W Luscinskas / Ninghai Wang / Cox Terhorst

    PLoS ONE, Vol 10, Iss 3, p e

    2015  Volume 0121968

    Abstract: ... migration. We conclude that Slamf1 and Slamf8 govern ROS-dependent innate immune responses of myeloid cells ... macrophages and neutrophils is accelerated. These opposing effects of Slamf1 and Slamf8 are cell-intrinsic ... Previous studies have demonstrated that the cell surface receptor Slamf1 (CD150) is requisite ...

    Abstract Previous studies have demonstrated that the cell surface receptor Slamf1 (CD150) is requisite for optimal NADPH-oxidase (Nox2) dependent reactive oxygen species (ROS) production by phagocytes in response to Gram- bacteria. By contrast, Slamf8 (CD353) is a negative regulator of ROS in response to Gram+ and Gram- bacteria. Employing in vivo migration after skin sensitization, induction of peritonitis, and repopulation of the small intestine demonstrates that in vivo migration of Slamf1-/- dendritic cells and macrophages is reduced, as compared to wt mice. By contrast, in vivo migration of Slamf8-/- dendritic cells, macrophages and neutrophils is accelerated. These opposing effects of Slamf1 and Slamf8 are cell-intrinsic as judged by in vitro migration in transwell chambers in response to CCL19, CCL21 or CSF-1. Importantly, inhibiting ROS production of Slamf8-/- macrophages by diphenyleneiodonium chloride blocks this in vitro migration. We conclude that Slamf1 and Slamf8 govern ROS-dependent innate immune responses of myeloid cells, thus modulating migration of these cells during inflammation in an opposing manner.
    Keywords Medicine ; R ; Science ; Q
    Language English
    Publishing date 2015-01-01T00:00:00Z
    Publisher Public Library of Science (PLoS)
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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