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PMID: 2886511 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Proteoglycans and glycosaminoglycans induce gap junction synthesis and function in primary liver cultures.

The Journal of cell biology ·Vol. 105 ·No. 1 ·1987-07-00 ·Pages 541-51

Spray DC, Fujita M, Saez JC, Choi H, Watanabe T, Hertzberg E, Rosenberg LC, Reid LM

Abstract

Intercellular communication via gap junctions, as measured by dye and electrical coupling, disappears within 12 h in primary rat hepatocytes cultured in serum-supplemented media or within 24 h in cells in a serum-free, hormonally defined medium (HDM) designed for hepatocytes. Glucagon and linoleic acid/BSA were the primary factors in the HDM responsible for the extended life span of the electrical coupling. After 24 h of culture, no hormone or growth factor tested could restore the expression of gap junctions. After 4-5 d of culture, the incidence of coupling was undetectable in a serum-supplemented medium and was only 4-5% in HDM alone. However, treatment with glycosaminoglycans or proteoglycans of 24-h cultures, having no detectable gap junction protein, resulted in synthesis of gap junction protein and of reexpression of electrical and dye coupling within 48 h. Most glycosaminoglycans were inactive (heparan sulfates, chondroitin-6 sulfates) or only weakly active (dermatan sulfates, chondroitin 4-sulfates, hyaluronates), the weakly active group increasing the incidence of coupling to 10-30% with the addition of 50-100 micrograms/ml of the factor. Treatment of the cells with 50-100 micrograms/ml of heparins derived from lung or intestine resulted in cells with intermediate levels of coupling (30-50%). By contrast, 10-20 micrograms/ml of chondroitin sulfate proteoglycan, dermatan sulfate proteoglycan, or liver-derived heparin resulted in dye coupling in 80-100% of the cells, with numerous cells showing dye spread from a single injected cell. Sulfated polysaccharides of glucose (dextran sulfates) or of galactose (carrageenans) were inactive or only weakly active except for lambda-carrageenan, which induced up to 70% coupling (albeit no multiple coupling in the cultures). The abundance of mRNA (Northern blots) encoding gap junction protein and the amounts of the 27-kD gap junction polypeptide (Western blots) correlated with the degree of electrical and dye coupling indicating that the active glycosaminoglycans and proteoglycans are inducing synthesis and expression of gap junctions. Thus, proteoglycans and glycosaminoglycans, especially those found in abundance in the extracellular matrix of liver cells, are important in the regulation of expression of gap junctions and, thereby, in the regulation of intercellular communication in the liver. The relative potencies of heparins from different tissue sources at inducing gap junction expression are suggestive of functional tissue specificity for these glycosaminoglycans.

MeSH Terms
Animals Cell Communication/drug effects Cells, Cultured Coloring Agents/metabolism Connexins Culture Media/analysis Gene Expression Regulation/drug effects Glycosaminoglycans/pharmacology Intercellular Junctions/drug effects,metabolism Kinetics Liver/cytology Liver Regeneration Male Membrane Potentials/drug effects Membrane Proteins/biosynthesis Polysaccharides/pharmacology Proteoglycans/pharmacology Rats Rats, Inbred Strains
Chemicals
Coloring Agents Connexins Culture Media Glycosaminoglycans Membrane Proteins Polysaccharides Proteoglycans
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Spray D C
Fujita M
Saez J C
Choi H
Watanabe T
Hertzberg E
Rosenberg L C
Reid L M
References (43)
43 references, click to expand
  1. Physiology of electrotonic junctions.
    Ann N Y Acad Sci. 1966 Jul 14;137(2):509-39 PMID: 5229812
  2. Electrophysiological properties of gap junctions between dissociated pairs of rat hepatocytes.
    J Cell Biol. 1986 Jul;103(1):135-44 PMID: 3722262
  3. Heparan sulfates of cultured cells. II. Acid-soluble and -precipitable species of different cell lines.
    Biochemistry. 1971 Apr 13;10(8):1445-51 PMID: 4253010
  4. Proteoglycans from bovine proximal humeral articular cartilage. Structural basis for the polydispersity of proteoglycan subunit.
    J Biol Chem. 1976 Oct 25;251(20):6439-44 PMID: 977583
  5. Suppression by heparin of smooth muscle cell proliferation in injured arteries.
    Nature. 1977 Feb 17;265(5595):625-6 PMID: 859561
  6. Loss and reappearance of gap junctions in regenerating liver.
    J Cell Biol. 1978 Aug;78(2):554-64 PMID: 690179
  7. Liver cells.
    Methods Enzymol. 1979;58:536-44 PMID: 423789
  8. Cytological changes in gap junctions during liver regeneration.
    J Ultrastruct Res. 1979 Jun;67(3):229-42 PMID: 458923
  9. Proteoglycans from bovine nasal cartilage. Properties of a soluble form of link protein.
    J Biol Chem. 1979 Oct 25;254(20):10523-31 PMID: 114526
  10. Number and evolutionary conservation of alpha- and beta-tubulin and cytoplasmic beta- and gamma-actin genes using specific cloned cDNA probes.
    Cell. 1980 May;20(1):95-105 PMID: 6893015
  11. Metabolism of sulfated glycosaminoglycans in rat hepatocytes. Synthesis of heparan sulfate and distribution into cellular and extracellular pools.
    Biochim Biophys Acta. 1980 Jul 3;630(3):402-13 PMID: 6446940
  12. Protein synthesis requires cell-surface contact while nuclear events respond to cell shape in anchorage-dependent fibroblasts.
    Cell. 1980 Sep;21(2):365-72 PMID: 6157481
  13. Liver plasma membranes and proteoglycan prepared therefrom inhibit the growth of hepatoma cells in vitro.
    Biochim Biophys Acta. 1981 Aug 6;646(1):161-8 PMID: 7023539
  14. Cartilage proteoglycans inhibit fibronectin-mediated adhesion.
    Nature. 1981 Sep 17-23;293(5829):224-6 PMID: 6792545
  15. Cultured endothelial cells produce a heparinlike inhibitor of smooth muscle cell growth.
    J Cell Biol. 1981 Aug;90(2):372-9 PMID: 7287812
  16. Five-hour half-life of mouse liver gap-junction protein.
    J Cell Biol. 1981 Aug;90(2):521-6 PMID: 7287816
  17. Intercellular communication in normal and regenerating rat liver: a quantitative analysis.
    J Cell Biol. 1981 Nov;91(2 Pt 1):505-23 PMID: 7309793
  18. Cell junction and cyclic AMP: 1. Upregulation of junctional membrane permeability and junctional membrane particles by administration of cyclic nucleotide or phosphodiesterase inhibitor.
    J Membr Biol. 1981;63(1-2):105-21 PMID: 6273566
  19. The extracellular matrix of the liver.
    Coll Relat Res. 1982 Mar;2(2):151-75 PMID: 7049553
  20. Co-existence of vinculin and a vinculin-like protein of higher molecular weight in smooth muscle.
    J Biol Chem. 1982 Sep 25;257(18):11024-31 PMID: 6809764
  21. Isolation and characterization of a 35,000 molecular weight subunit fetal cartilage matrix protein.
    J Biol Chem. 1983 Jan 10;258(1):655-61 PMID: 6401297
  22. Anti-HLA antibodies of predetermined specificity: a chemically synthesized peptide induces antibodies specific for HLA-A,B heavy chain.
    Proc Natl Acad Sci U S A. 1983 Jan;80(1):255-8 PMID: 6571999
  23. Cell surface heparan sulfate mediates some adhesive responses to glycosaminoglycan-binding matrices, including fibronectin.
    J Cell Biol. 1983 Jan;96(1):112-23 PMID: 6219115
  24. Regulation of growth and differentiation of a rat hepatoma cell line by the synergistic interactions of hormones and collagenous substrata.
    J Cell Biol. 1983 Oct;97(4):1179-90 PMID: 6137487
  25. Structure and properties of an under-sulfated heparan sulfate proteoglycan synthesized by a rat hepatoma cell line.
    J Cell Biol. 1984 Mar;98(3):946-53 PMID: 6230367
  26. Hepatocyte proliferation in vitro: its dependence on the use of serum-free hormonally defined medium and substrata of extracellular matrix.
    Proc Natl Acad Sci U S A. 1984 Mar;81(5):1411-5 PMID: 6584889
  27. Culturing hepatocytes and other differentiated cells.
    Hepatology. 1984 May-Jun;4(3):548-59 PMID: 6373552
  28. "A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum.
    Anal Biochem. 1984 Feb;137(1):266-7 PMID: 6329026
  29. A detergent-independent procedure for the isolation of gap junctions from rat liver.
    J Biol Chem. 1984 Aug 10;259(15):9936-43 PMID: 6086660
  30. Determination of synaptic phenotype: insulin and cAMP independently initiate development of electrotonic coupling between cultured sympathetic neurons.
    Proc Natl Acad Sci U S A. 1984 Oct;81(19):6235-9 PMID: 6091144
  31. A protein homologous to the 27,000 dalton liver gap junction protein is present in a wide variety of species and tissues.
    Cell. 1984 Nov;39(1):61-9 PMID: 6091916
  32. Posttranscriptional modulation of gene expression in cultured rat hepatocytes.
    Mol Cell Biol. 1984 Sep;4(9):1929-34 PMID: 6333585
  33. Heparin regulates the collagen phenotype of vascular smooth muscle cells: induced synthesis of an Mr 60,000 collagen.
    J Cell Biol. 1985 Feb;100(2):613-9 PMID: 3968183
  34. Heparinlike molecules with anticoagulant activity are synthesized by cultured endothelial cells.
    Biochem Biophys Res Commun. 1985 Jan 16;126(1):365-72 PMID: 3970699
  35. An antiproliferative heparan sulfate species produced by postconfluent smooth muscle cells.
    J Cell Biol. 1985 Apr;100(4):1041-9 PMID: 3156864
  36. Physiology and pharmacology of gap junctions.
    Annu Rev Physiol. 1985;47:281-303 PMID: 2859833
  37. Isolation of dermatan sulfate proteoglycans from mature bovine articular cartilages.
    J Biol Chem. 1985 May 25;260(10):6304-13 PMID: 3997823
  38. Regulation of gap junctional conductance.
    Am J Physiol. 1985 Jun;248(6 Pt 2):H753-64 PMID: 2408489
  39. Platelet-derived growth factor and heparin-like glycosaminoglycans regulate thrombospondin synthesis and deposition in the matrix by smooth muscle cells.
    J Cell Biol. 1985 Sep;101(3):1059-70 PMID: 4030891
  40. A unique heparan sulfate in the nuclei of hepatocytes: structural changes with the growth state of the cells.
    J Cell Biol. 1986 Feb;102(2):587-99 PMID: 2935544
  41. cAMP increases junctional conductance and stimulates phosphorylation of the 27-kDa principal gap junction polypeptide.
    Proc Natl Acad Sci U S A. 1986 Apr;83(8):2473-7 PMID: 3010311
  42. Molecular cloning of cDNA for rat liver gap junction protein.
    J Cell Biol. 1986 Jul;103(1):123-34 PMID: 3013898
  43. High-yield preparation of isolated rat liver parenchymal cells: a biochemical and fine structural study.
    J Cell Biol. 1969 Dec;43(3):506-20 PMID: 4900611
Article Info
Journal
The Journal of cell biology
Abbr.
J Cell Biol
ISSN
0021-9525
Published
1987-07-00
Pages
541-51
Language
English
Region
United States
NLM ID
0375356
PMCID
PMC2114879
Subset
IM
Grants
NIADDK NIH HHS · AM17702-12 · United States
NIADDK NIH HHS · AM34614-01 · United States
NCI NIH HHS · P30-CA13330 · United States
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