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Defining the in vivo function of Siglec-F, a CD33-related Siglec expressed on mouse eosinophils.

Defining the in vivo function of Siglec-F, a CD33-related Siglec expressed on mouse eosinophils. Research Abstract Details 

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  • Defining the in vivo function of Siglec-F, a CD33-related Siglec expressed on mouse eosinophils. Abstract Text:

    mai zhangMai Zhang,takashi angataTakashi Angata,jae youn choJae Youn Cho,marina millerMarina Miller,david h broideDavid H Broide,ajit varkiAjit Varki,

    CD33-related Siglecs (CD33rSiglecs) are a family of sialic acid-recognizing lectins on immune cells whose biologic functions are unknown. We studied in vivo functions of Siglec-F, the CD33rSiglec expressed on mouse eosinophils, which are prominent in allergic processes. Induction of allergic lung inflammation in mice caused up-regulation of Siglec-F on blood and bone marrow eosinophils, accompanied by newly induced expression on some CD4(+) cells, as well as quantitative up-regulation of endogenous Siglec-F ligands in the lung tissue and airways. Taken together with the tyrosine-based inhibitory motif in the cytosolic tail of Siglec-F, the data suggested a negative feedback loop, controlling allergic responses of eosinophils and helper T cells, via Siglec-F and Siglec-F ligands. To pursue this hypothesis, we created Siglec-F-null mice. Allergen-challenged null mice showed increased lung eosinophil infiltration, enhanced bone marrow and blood eosinophilia, delayed resolution of lung eosinophilia, and reduced peribronchial-cell apoptosis. Anti-Siglec-F antibody cross-linking also enhanced eosinophil apoptosis in vitro. These data support the proposed negative feedback role for Siglec-F, represent the first in vivo demonstration of biologic functions for any CD33rSiglec, and predict a role for human Siglec-8 (the isofunctional paralog of mouse Siglec-F) in regulating the pathogenesis of human eosinophil-mediated disorders.

    Defining the in vivo function of Siglec-F, a CD33-related Siglec expressed on mouse eosinophils. Publishing Authors By Initials

    m zhangM Zhang,t angataT Angata,jy choJY Cho,m millerM Miller,dh broideDH Broide,a varkiA Varki,

    For similar cells: blood cells: leukocytes: leukocytes, mononuclear: lymphocytes: t-lymphocytes research abstracts see: cells: blood cells: leukocytes: leukocytes, mononuclear: lymphocytes: t-lymphocytes research

    PUBMED ID PMID:

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    Defining the in vivo function of Siglec-F, a CD33-related Siglec expressed on mouse eosinophils. Journal Published:

    PUBLICATION TYPE: Research Support, N.I.H., Extr

    Journal: Blood

    VOLUME: 109

    Page Numbers: 4280-7

    Journal Abbreviation:

    ISSN: 0006-4971

    DAY: 1

    MONTH: 02

    YEAR: 2007

    Defining the in vivo function of Siglec-F, a CD33-related Siglec expressed on mouse eosinophils. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 7603509

    Defining the in vivo function of Siglec-F, a CD33-related Siglec expressed on mouse eosinophils. Keywords Mesh Terms:

    KEYWORDS: T-Lymphocytes

    MESH TERMS: metabolism

    Chemical & Substance for Abstract: Defining the in vivo function of Siglec-F, a CD33-related Siglec expressed on mouse eosinophils. Information

    Substance Name: N-Acetylneuraminic Acid

    Registry Number: 131-48-6

    Grant and Affiliation Information for Defining the in vivo function of Siglec-F, a CD33-related Siglec expressed on mouse eosinophils.

    AFFILIATION: Glycobiology Research and Training Center, Departments of Medicine and Cellular & Molecular Medicine, and Biomedical Sciences Graduate Program, University of California at San Diego, La Jolla, CA 92093-0687, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NHLBI

    GRANT: HL57345

    ACRONYM: HL

    MEDLINETA: Blood

    REFSOURCE:

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    ACCESSION NUMBER:

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