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Research article2011Peer reviewedOpen access

Serglycin Is a Major Proteoglycan in Polarized Human Endothelial Cells and Is Implicated in the Secretion of the Chemokine GRO alpha/CXCL1

Meen, AJ; Øynebråten, I; Reine, TM; Duelli, A; Svennevig, K; Pejler, Gunnar; Jensen, T; Kolset, SO

Abstract

Proteoglycan (PG) expression was studied in primary human umbilical vein endothelial cells (HUVEC). RT-PCR analyses showed that the expression of the PG serglycin core protein was much higher than that of the extracellular matrix PG decorin and the cell surface PG syndecan-1. PG biosynthesis was further studied by biosynthetic [(35)S] sulfate labeling of polarized HUVEC. Interestingly, a major part of (35)S-PGs was secreted to the apical medium. A large portion of these PGs was trypsin-resistant, a typical feature of serglycin. The trypsin-resistant PGs were mainly of the chondroitin/dermatan sulfate type but also contained a minor heparan sulfate component. Secreted serglycin was identified by immunoprecipitation as a PG with a core protein of similar to 30 kDa. Serglycin was furthermore shown to be present in perinuclear regions and in two distinct types of vesicles throughout the cytoplasm using immunocytochemistry. To search for possible serglycin partner molecules, HUVEC were stained for the chemokine growth-related oncogene alpha(GRO alpha/CXCL1). Co-localization with serglycin could be demonstrated, although not in all vesicles. Serglycin did not show overt co-localization with tissue-type plasminogen activator-positive vesicles. When PG biosynthesis was abrogated using benzyl-beta-D-xyloside, serglycin secretion was decreased, and the number of vesicles with co-localized serglycin and GRO alpha was reduced. The level of GRO alpha in the apical medium was also reduced after xyloside treatment. Together, these findings indicate that serglycin is a major PG in human endothelial cells, mainly secreted to the apical medium and implicated in chemokine secretion.

Published in

Journal of Biological Chemistry
2011, Volume: 286, number: 4, pages: 2636-2647 Publisher: AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC

    UKÄ Subject classification

    Biochemistry and Molecular Biology

    Publication identifier

    DOI: https://doi.org/10.1074/jbc.M110.151944

    Permanent link to this page (URI)

    https://res.slu.se/id/publ/47407