Literature DB >> 7015344

Sulfated and nonsulfated glycosaminoglycans and glycopeptides are synthesized by kidney in vivo and incorporated into glomerular basement membranes.

M C Lemkin, M G Farquhar.   

Abstract

The biosynthesis of glycosaminoglycans (GAG) and glycopeptides was studied in rat kidney cortex, glomeruli, and isolated glomerular basement membranes (GBM). Rats were given four intraperitoneal injections of [(35)S]sulfate and [(3)H]glucosamine (over 10 hr) and sacrificed 14 hr after the last injection. Fractions of kidney glomeruli and purified GBM were prepared. The percent of the label incorporated into specific GAG or into glycopeptides was determined by selective degradative techniques in conjunction with gel filtration chromatography using the methods of Hart [Hart, G. W. (1976) J. Biol. Chem. 251, 6513-6521; Hart, G. W. (1978) Dev. Biol. 62, 78-98]. After digestion with Pronase and chromatography on Sephadex G-50, approximately 68% of the total (35)S radioactivity and 10-15% of the total (3)H radioactivity incorporated into cortex, glomeruli, or GBM was found in the GAG fraction, and the remainder ( approximately 32% of (35)S radioactivity and 85-90% of the (3)H radioactivity) was found in glycopeptide fractions. Treatment of GAG fractions isolated from the three sources (cortex, glomeruli, and GBM) with nitrous acid (which degrades heparan sulfates) indicated that the majority (85%, 65%, and 87%) of the (35)S radioactivity as well as the majority (60%, 50%, and 91%) of the (3)H radioactivity from all three sources was degraded by this treatment. When nitrous acid-resistant GAG from GBM were subjected to digestion with Streptomyces hyaluronidase (which degrades hyaluronic acid), approximately 6% of the (3)H-labeled material was sensitive to this treatment. The remaining (35)S- and (3)H-labeled GAG isolated from GBM were digested with chondroitinase ABC (which degrades chondroitin sulfates A and C and dermatan sulfate). Although the ratios of the types of GAG synthesized by all three sources were similar, in GBM the ratios of (35)S- to (3)H-labeled GAG and of (3)H-labeled glycopeptides to (3)H-labeled GAG were higher (2.5 times) than those found for glomeruli. The data demonstrate the synthesis of both sulfated and nonsulfated GAG by rat kidney cortex and glomeruli and their transport to and incorporation into the GBM. Heparan sulfate is the major GAG synthesized by glomeruli, but the glomeruli also synthesize smaller amounts of hyaluronic acid and chondroitin sulfates, which are in part incorporated into GBM. In addition, the renal cortex and the glomeruli synthesize glycopeptides, some of which are sulfated, and incorporate them into GBM.

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Year:  1981        PMID: 7015344      PMCID: PMC319206          DOI: 10.1073/pnas.78.3.1726

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  24 in total

1.  Heparan sulfate biosynthesis by embryonic tissues and primary fibroblast populations.

Authors:  G W Conrad; G W Hart
Journal:  Dev Biol       Date:  1975-06       Impact factor: 3.582

2.  Localization of the nephrotoxic antigen within the isolated renal glomerulus.

Authors:  C A KRAKOWER; S A GREENSPON
Journal:  AMA Arch Pathol       Date:  1951-06

3.  Synthesis of sulfated glycosaminoglycans by embryonic corneal epithelium.

Authors:  S Meier; E D Hay
Journal:  Dev Biol       Date:  1973-12       Impact factor: 3.582

4.  The distribution of 2-acetamido-2-deoxy-D-glucose residues in mammalian heparins.

Authors:  J A Cifonelli; J King
Journal:  Carbohydr Res       Date:  1972-02       Impact factor: 2.104

5.  Sulfated glycopeptides from rat brain glycoproteins.

Authors:  R K Margolis; R U Margolis
Journal:  Biochemistry       Date:  1970-10-27       Impact factor: 3.162

6.  Structural studies on heparins with unusually high N-acetylglucosamine contents.

Authors:  J A Cifonelli; J King
Journal:  Biochim Biophys Acta       Date:  1973-09-14

7.  Fluorescamine: a reagent for assay of amino acids, peptides, proteins, and primary amines in the picomole range.

Authors:  S Udenfriend; S Stein; P Böhlen; W Dairman; W Leimgruber; M Weigele
Journal:  Science       Date:  1972-11-24       Impact factor: 47.728

8.  Purification and properties of bacterial chondroitinases and chondrosulfatases.

Authors:  T Yamagata; H Saito; O Habuchi; S Suzuki
Journal:  J Biol Chem       Date:  1968-04-10       Impact factor: 5.157

9.  Glycosaminoglycan synthesis by embryonic inductors: neural tube, notochord, and lens.

Authors:  E D Hay; S Meier
Journal:  J Cell Biol       Date:  1974-09       Impact factor: 10.539

10.  Epithelial collagens and glycosaminoglycans in the embryonic cornea. Macromolecular order and morphogenesis in the basement membrane.

Authors:  R L Trelstad; K Hayashi; B P Toole
Journal:  J Cell Biol       Date:  1974-09       Impact factor: 10.539

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  16 in total

1.  Basement membrane heparan sulfate proteoglycan is the main proteoglycan synthesized by glomerular epithelial cells in culture.

Authors:  J L Stow; C J Soroka; K MacKay; L Striker; G Striker; M G Farquhar
Journal:  Am J Pathol       Date:  1989-10       Impact factor: 4.307

2.  Basement membrane heparan sulfate proteoglycans are concentrated in the laminae rarae and in podocytes of the rat renal glomerulus.

Authors:  J L Stow; H Sawada; M G Farquhar
Journal:  Proc Natl Acad Sci U S A       Date:  1985-05       Impact factor: 11.205

Review 3.  Antigens of the human glomerular basement membrane.

Authors:  L S Fouser; A F Michael
Journal:  Springer Semin Immunopathol       Date:  1987

4.  Tissue distribution of amyloid P component as defined by a monoclonal antibody produced by immunization with human glomerular basement membranes.

Authors:  H al-Mutlaq; J Wheeler; H Robertson; C Watchorn; A R Morley
Journal:  Histochem J       Date:  1993-03

5.  Cell associated glycoproteins synthesized by cultured renal tubular cells.

Authors:  W W Minuth
Journal:  Histochemistry       Date:  1982

6.  Histochemical localization of skin glycosaminoglycans during feather development in the chick embryo.

Authors:  Colin A B Jahoda; Annick Mauger; Philippe Sengel
Journal:  Rouxs Arch Dev Biol       Date:  1987-07

7.  Chondroitin sulfate proteoglycan is a constituent of the basement membrane in the rat embryo parietal yolk sac.

Authors:  R V Iozzo; C C Clark
Journal:  Histochemistry       Date:  1987

8.  Renal glomerular proteoglycans. An investigation of their synthesis in vivo using a technique for fixation in situ.

Authors:  L A Beavan; M Davies; R M Mason
Journal:  Biochem J       Date:  1988-04-15       Impact factor: 3.857

9.  Glomerular anionic site distribution in nonproteinuric rats. A computer-assisted morphometric analysis.

Authors:  P A Pilia; R P Swain; A V Williams; C B Loadholt; S K Ainsworth
Journal:  Am J Pathol       Date:  1985-12       Impact factor: 4.307

10.  Regulation of glomerular endothelial cell proteoglycans by glucose.

Authors:  Tae-Sun Ha; Senthil Duraisamy; Jennifer L Faulkner; Balakuntalam S Kasinath
Journal:  J Korean Med Sci       Date:  2004-04       Impact factor: 2.153

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