Literature DB >> 3292336

Formation of extracellular matrix in normal rat liver: lipocytes as a major source of proteoglycan.

D M Arenson1, S L Friedman, D M Bissell.   

Abstract

Proteoglycans are a major component of the normal hepatic extracellular matrix and undergo quantitative and qualitative changes in hepatic fibrosis. The cellular sources of proteoglycans are as yet incompletely defined. We examined this question using primary cultures of hepatocytes and lipocytes isolated from normal rat liver. Proteoglycan synthesis was assessed by measuring production of sulfated glycosaminoglycan, the polysaccharide moiety of proteoglycans. The findings indicate that lipocytes produce sixfold more glycosaminoglycan, per cell, than do hepatocytes. Two-thirds of the newly synthesized material is cell- or matrix-associated. Of the individual glycosaminoglycan species produced by lipocytes, dermatan sulfate represents 60% of the total; heparan sulfate and chondroitin sulfate are measurable but relatively minor. In hepatocyte cultures, heparan sulfate accounted for essentially all of the glycosaminoglycan detected. We conclude that lipocytes are an important source of proteoglycan in normal liver and may be the principal source of dermatan sulfate associated with hepatic fibrosis.

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Year:  1988        PMID: 3292336     DOI: 10.1016/0016-5085(88)90502-1

Source DB:  PubMed          Journal:  Gastroenterology        ISSN: 0016-5085            Impact factor:   22.682


  22 in total

1.  Soluble Arg-Gly-Asp peptides reduce collagen accumulation in cultured rat hepatic stellate cells.

Authors:  H Iwamoto; H Sakai; K Kotoh; M Nakamuta; H Nawata
Journal:  Dig Dis Sci       Date:  1999-05       Impact factor: 3.199

2.  Effects of glycyrrhetinic acid on collagen metabolism of hepatic stellate cells at different stages of liver fibrosis in rats.

Authors:  J Y Wang; Q S Zhang; J S Guo; M Y Hu
Journal:  World J Gastroenterol       Date:  2001-02       Impact factor: 5.742

3.  One of the major sulphated proteins secreted by rat hepatocytes contains low-sulphated chondroitin sulphate.

Authors:  E M Sjöberg; E Fries
Journal:  Biochem J       Date:  1990-11-15       Impact factor: 3.857

Review 4.  Matrix metalloproteinases, the pros and cons, in liver fibrosis.

Authors:  Yuan-Ping Han
Journal:  J Gastroenterol Hepatol       Date:  2006-10       Impact factor: 4.029

5.  Contribution to the study of septal fibrosis of the liver.

Authors:  Z A Andrade
Journal:  Int J Exp Pathol       Date:  1991-10       Impact factor: 1.925

6.  Immunolocalization of proliferating perisinusoidal cells in rat liver.

Authors:  S J Johnson; J E Hines; A D Burt
Journal:  Histochem J       Date:  1992-02

Review 7.  Molecular mechanisms of hepatic fibrosis and principles of therapy.

Authors:  S L Friedman
Journal:  J Gastroenterol       Date:  1997-06       Impact factor: 7.527

8.  Activation of cultured rat hepatic lipocytes by Kupffer cell conditioned medium. Direct enhancement of matrix synthesis and stimulation of cell proliferation via induction of platelet-derived growth factor receptors.

Authors:  S L Friedman; M J Arthur
Journal:  J Clin Invest       Date:  1989-12       Impact factor: 14.808

9.  Lipocytes from normal rat liver release a neutral metalloproteinase that degrades basement membrane (type IV) collagen.

Authors:  M J Arthur; S L Friedman; F J Roll; D M Bissell
Journal:  J Clin Invest       Date:  1989-10       Impact factor: 14.808

10.  Purification and partial characterization of the major cell-associated heparan sulphate proteoglycan of rat liver.

Authors:  M Lyon; J T Gallagher
Journal:  Biochem J       Date:  1991-01-15       Impact factor: 3.857

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