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Initiation of protein O glycosylation by the polypeptide GalNAcT-1 in vascular biology and humoral immunity.

Initiation of protein O glycosylation by the polypeptide GalNAcT-1 in vascular biology and humoral immunity. Research Abstract Details 

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  • Initiation of protein O glycosylation by the polypeptide GalNAcT-1 in vascular biology and humoral immunity. Abstract Text:

    mari tennoMari Tenno,kazuaki ohtsuboKazuaki Ohtsubo,fred k hagenFred K Hagen,david dittoDavid Ditto,alexander zarbockAlexander Zarbock,patrick schaerliPatrick Schaerli,ulrich h von andrianUlrich H von Andrian,klaus leyKlaus Ley,dzung leDzung Le,lawrence a tabakLawrence A Tabak,jamey d marthJamey D Marth,mari tennoMari Tenno,kazuaki ohtsuboKazuaki Ohtsubo,fred k hagenFred K Hagen,david dittoDavid Ditto,alexander zarbockAlexander Zarbock,patrick schaerliPatrick Schaerli,ulrich h von andrianUlrich H von Andrian,klaus leyKlaus Ley,dzung leDzung Le,lawrence a tabakLawrence A Tabak,jamey d marthJamey D Marth,

    Core-type protein O glycosylation is initiated by polypeptide N-acetylgalactosamine (GalNAc) transferase (ppGalNAcT) activity and produces the covalent linkage of serine and threonine residues of proteins. More than a dozen ppGalNAcTs operate within multicellular organisms, and they differ with respect to expression patterns and substrate selectivity. These distinctive features imply that each ppGalNAcT may differentially modulate regulatory processes in animal development, physiology, and perhaps disease. We found that ppGalNAcT-1 plays key roles in cell and glycoprotein selective functions that modulate the hematopoietic system. Loss of ppGalNAcT-1 activity in the mouse results in a bleeding disorder which tracks with reduced plasma levels of blood coagulation factors V, VII, VIII, IX, X, and XII. ppGalNAcT-1 further supports leukocyte trafficking and residency in normal homeostatic physiology as well as during inflammatory responses, in part by providing a scaffold for the synthesis of selectin ligands expressed by neutrophils and endothelial cells of peripheral lymph nodes. Animals lacking ppGalNAcT-1 are also markedly impaired in immunoglobulin G production, coincident with increased germinal center B-cell apoptosis and reduced levels of plasma B cells. These findings reveal that the initiation of protein O glycosylation by ppGalNAcT-1 provides a distinctive repertoire of advantageous functions that support vascular responses and humoral immunity.

    Initiation of protein O glycosylation by the polypeptide GalNAcT-1 in vascular biology and humoral immunity. Publishing Authors By Initials

    m tennoM Tenno,k ohtsuboK Ohtsubo,fk hagenFK Hagen,d dittoD Ditto,a zarbockA Zarbock,p schaerliP Schaerli,uh von andrianUH von Andrian,k leyK Ley,d leD Le,la tabakLA Tabak,jd marthJD Marth,m tennoM Tenno,k ohtsuboK Ohtsubo,fk hagenFK Hagen,d dittoD Ditto,a zarbockA Zarbock,p schaerliP Schaerli,uh von andrianUH von Andrian,k leyK Ley,d leD Le,la tabakLA Tabak,jd marthJD Marth,

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    Initiation of protein O glycosylation by the polypeptide GalNAcT-1 in vascular biology and humoral immunity. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Molecular and cellular biology

    VOLUME: 27

    Page Numbers: 8783-96

    Journal Abbreviation: Mol. Cell. Biol.

    ISSN: 1098-5549

    DAY: 8

    MONTH: 10

    YEAR: 2007

    Initiation of protein O glycosylation by the polypeptide GalNAcT-1 in vascular biology and humoral immunity. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 8109087

    Initiation of protein O glycosylation by the polypeptide GalNAcT-1 in vascular biology and humoral immunity. Keywords Mesh Terms:

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    Chemical & Substance for Abstract: Initiation of protein O glycosylation by the polypeptide GalNAcT-1 in vascular biology and humoral immunity. Information

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    Grant and Affiliation Information for Initiation of protein O glycosylation by the polypeptide GalNAcT-1 in vascular biology and humoral immunity.

    AFFILIATION: Howard Hughes Medical Institute, University of California San Diego, 9500 Gilman Drive, La Jolla, CA 92093, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIDDK

    GRANT: DK48247

    ACRONYM: DK

    MEDLINETA: Mol Cell Biol

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