Literature DB >> 3161884

Heparan sulfate proteoglycans of rat embryo fibroblasts. A hydrophobic form may link cytoskeleton and matrix components.

A Woods, J R Couchman, M Höök.   

Abstract

Heparan sulfate proteoglycans (HSPGs) synthesized in cultures of rat embryo fibroblasts have been isolated and characterized. Cells grown in the presence of [35S]sulfate secreted a large amount of radiolabeled macromolecules into the culture medium of which only a small proportion was identified as HSPG. However, the majority of radiolabeled proteoglycans isolated from the cell layer were HSPGs. Here, two types of HSPG were detected. One type had an Mr of 5-8 X 10(5) as estimated by gel chromatography on Sepharose CL-4B in the presence of 0.1% sodium dodecyl sulfate and lacked hydrophobic properties in that it showed no affinity for octyl-Sepharose and could not be inserted into liposomes. The other HSPG type had an estimated Mr of 3-5 X 10(5), was retained on octyl-Sepharose, and could be inserted into liposomes. In addition, the cells contained low molecular weight heparan sulfate oligosaccharides. Treatment of living cells with 0.2% Triton X-100, which retained stress fibers and extracellular matrix but solubilized cell membranes, released a proportion of the smaller HSPG together with the heparan sulfate oligosaccharides. The cytoskeleton-matrix residue remaining after detergent extraction of the cell contained the larger species of HSPG in addition to the smaller HSPG. The presence of the smaller hydrophobic HSPG in the detergent-treated cytoskeleton-matrix preparations suggests that it may form part of a transmembrane cytoskeleton-matrix linkage.

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Year:  1985        PMID: 3161884

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  31 in total

1.  Kinetic analysis of the effects of glycosaminoglycans and lipoproteins on urokinase-mediated plasminogen activation.

Authors:  J M Edelberg; M Weissler; S V Pizzo
Journal:  Biochem J       Date:  1991-06-15       Impact factor: 3.857

Review 2.  Biological functions of proteoglycans: use of specific inhibitors of proteoglycan synthesis.

Authors:  D J Carey
Journal:  Mol Cell Biochem       Date:  1991 May 29-Jun 12       Impact factor: 3.396

3.  Phosphorylation of a membrane-intercalated proteoglycan, syndecan-2, expressed in a stroma-inducing clone from a mouse Lewis lung carcinoma.

Authors:  N Itano; K Oguri; Y Nagayasu; Y Kusano; H Nakanishi; G David; M Okayama
Journal:  Biochem J       Date:  1996-05-01       Impact factor: 3.857

4.  Extracellular accumulation of small dermatan sulphate proteoglycan II by interference with the secretion-recapture pathway.

Authors:  G Schmidt; H Hausser; H Kresse
Journal:  Biochem J       Date:  1990-03-01       Impact factor: 3.857

Review 5.  Fell-Muir Lecture: Syndecans: from peripheral coreceptors to mainstream regulators of cell behaviour.

Authors:  John R Couchman; Sandeep Gopal; Hooi Ching Lim; Steffen Nørgaard; Hinke A B Multhaupt
Journal:  Int J Exp Pathol       Date:  2014-12-26       Impact factor: 1.925

6.  Identification of a 64 kDa heparan sulphate proteoglycan core protein from human lung fibroblast plasma membranes with a monoclonal antibody.

Authors:  H de Boeck; V Lories; G David; J J Cassiman; H van den Berghe
Journal:  Biochem J       Date:  1987-11-01       Impact factor: 3.857

Review 7.  Interaction of the cytoskeleton with the plasma membrane.

Authors:  V Niggli; M M Burger
Journal:  J Membr Biol       Date:  1987       Impact factor: 1.843

8.  Membrane associated proteoglycans in rat testicular peritubular cells.

Authors:  L Bichoualne; B Thiébot; M Langris; P Barbey; H Oulhaj; J Bocquet
Journal:  Mol Cell Biochem       Date:  1994-11-09       Impact factor: 3.396

9.  Accumulation of heparan sulfate in the culture of human melanoma cells with different metastatic ability.

Authors:  M Moczar; F Caux; M Bailly; O Berthier; J F Doré
Journal:  Clin Exp Metastasis       Date:  1993-11       Impact factor: 5.150

10.  Syndecan 4 heparan sulfate proteoglycan is a selectively enriched and widespread focal adhesion component.

Authors:  A Woods; J R Couchman
Journal:  Mol Biol Cell       Date:  1994-02       Impact factor: 4.138

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