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PMID: 1860887 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Induced expression of syndecan in healing wounds.

The Journal of cell biology ·Vol. 114 ·No. 3 ·1991-08-00 ·Pages 585-95

Elenius K, Vainio S, Laato M, Salmivirta M, Thesleff I, Jalkanen M

Abstract

We have studied the expression of an integral cell surface proteoglycan, syndecan, during the healing of cutaneous wounds, using immunohistochemical and in situ hybridization methods. In normal mouse skin, both syndecan antigen and mRNA were found to be expressed exclusively by epidermal and hair follicle cells. After incision and subsequent suturing, remarkably increased amounts of syndecan on the cell surfaces of migrating and proliferating epidermal cells and on hair follicle cells adjacent to wound margins were noted. This increased syndecan expression was shown to be a consequence of greater amounts of syndecan mRNA. Induction was observed already 1 d after wounding, was most significant at the time of intense cell proliferation, and was still observable 14 d after incision. The migrating cells of the leading edge of the epithelium also showed enhanced syndecan expression, although clearly less than that seen in the proliferating epithelium. The merging epithelial cells at the site of incision showed little or no syndecan expression; increased syndecan expression, however, was detected during later epithelial stratification. When wounds were left unsutured, in situ hybridization experiments also revealed scattered syndecan-positive signals in the granulation tissue near the migrating epidermal sheet. By immunohistochemical analysis, positive staining in granulation tissue was observed around vascular endothelial cells in a subpopulation of growing capillaries. Induction of syndecan in granulation tissue both at the protein and mRNA levels was temporally and spatially highly restricted. Granulation tissue, which formed in viscose cellulose sponge cylinders placed under the skin of rats, was also found to produce 3.4 and 2.6 kb mRNA species of syndecan similar to that observed in the normal murine mammary epithelial cell line, NMuMG. These results suggest that syndecan may have a unique and important role as a cell adhesion and a growth factor-binding molecule not only during embryogenesis but also during tissue regeneration in mature tissues.

MeSH Terms
Animals Cell Differentiation Cell Line Cell Movement Endothelium, Vascular/metabolism Granulation Tissue/metabolism Immunohistochemistry Keratinocytes/cytology Male Membrane Glycoproteins/biosynthesis Mice Mice, Inbred BALB C Nucleic Acid Hybridization Proteoglycans/biosynthesis Skin/cytology,injuries,metabolism Syndecans Wound Healing
Chemicals
Membrane Glycoproteins Proteoglycans Syndecans
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Elenius K
Department of Medical Biochemistry, University of Turku, Finland.
Vainio S
Laato M
Salmivirta M
Thesleff I
Jalkanen M
References (53)
53 references, click to expand
  1. Binding of human syndecan to extracellular matrix proteins.
    J Biol Chem. 1990 Oct 15;265(29):17837-43 PMID: 1698781
  2. Oxygen and carbon dioxide tensions in experimental wounds.
    Surg Gynecol Obstet. 1971 Dec;133(6):1003-7 PMID: 5117384
  3. Proteoglycans as modulators of growth factor activities.
    Cell. 1991 Mar 8;64(5):867-9 PMID: 2001586
  4. Cell surface proteoglycan expression correlates with epithelial-mesenchymal interaction during tooth morphogenesis.
    Dev Biol. 1988 Oct;129(2):565-72 PMID: 3417053
  5. Accelerated healing of incisional wounds in rats induced by transforming growth factor-beta.
    Science. 1987 Sep 11;237(4820):1333-6 PMID: 2442813
  6. Cell surface proteoglycan binds mouse mammary epithelial cells to fibronectin and behaves as a receptor for interstitial matrix.
    J Cell Biol. 1988 Feb;106(2):423-30 PMID: 2963012
  7. A method for the covalent attachment of cells to glass slides for use in immunohistochemical assays.
    Am J Clin Pathol. 1985 Mar;83(3):356-63 PMID: 2579542
  8. Urokinase- and tissue-type plasminogen activators in keratinocytes during wound reepithelialization in vivo.
    J Invest Dermatol. 1988 Jun;90(6):790-5 PMID: 3131440
  9. The heparin-binding (fibroblast) growth factor family of proteins.
    Annu Rev Biochem. 1989;58:575-606 PMID: 2549857
  10. The local effect of neutral salt-soluble collagen on the formation of granulation tissue.
    Ann Med Exp Biol Fenn. 1962;40:118-27 PMID: 13925971
  11. Syndecan from embryonic tooth mesenchyme binds tenascin.
    J Biol Chem. 1991 Apr 25;266(12):7733-9 PMID: 1708391
  12. Heparan sulfate-mediated binding of epithelial cell surface proteoglycan to thrombospondin.
    J Biol Chem. 1989 Feb 15;264(5):2885-9 PMID: 2521631
  13. Induction of tenascin in healing wounds.
    J Cell Biol. 1988 Dec;107(6 Pt 2):2757-67 PMID: 2462568
  14. Immunocytochemistry of cell surface heparan sulfate proteoglycan in mouse tissues. A light and electron microscopic study.
    J Histochem Cytochem. 1987 Oct;35(10):1079-88 PMID: 2957423
  15. Hormonal modification of epithelial differentiation and expression of cell surface heparan sulfate proteoglycan in the mouse vaginal epithelium. An immunohistochemical and electron microscopic study.
    Lab Invest. 1988 Jan;58(1):68-76 PMID: 2961930
  16. Mouse mammary epithelial cells produce basement membrane and cell surface heparan sulfate proteoglycans containing distinct core proteins.
    J Cell Biol. 1988 Mar;106(3):953-62 PMID: 2964452
  17. Heparan sulfate proteoglycans from mouse mammary epithelial cells. Cell surface proteoglycan as a receptor for interstitial collagens.
    J Biol Chem. 1985 Jul 5;260(13):8157-62 PMID: 3159726
  18. Heparan sulfate proteoglycans from mouse mammary epithelial cells: localization on the cell surface with a monoclonal antibody.
    J Cell Biol. 1985 Sep;101(3):976-84 PMID: 3161899
  19. The cell surface proteoglycan from mouse mammary epithelial cells bears chondroitin sulfate and heparan sulfate glycosaminoglycans.
    J Biol Chem. 1985 Sep 15;260(20):11046-52 PMID: 3161889
  20. New perspectives in cell adhesion: RGD and integrins.
    Science. 1987 Oct 23;238(4826):491-7 PMID: 2821619
  21. Integrins: a family of cell surface receptors.
    Cell. 1987 Feb 27;48(4):549-54 PMID: 3028640
  22. Cell surface proteoglycan associates with the cytoskeleton at the basolateral cell surface of mouse mammary epithelial cells.
    J Cell Biol. 1986 Dec;103(6 Pt 2):2683-96 PMID: 3025223
  23. Potential roles of fibronectin in cutaneous wound repair.
    Arch Dermatol. 1988 Feb;124(2):201-6 PMID: 3124772
  24. Molecular polymorphism of a cell surface proteoglycan: distinct structures on simple and stratified epithelia.
    Proc Natl Acad Sci U S A. 1988 Dec;85(24):9562-6 PMID: 3144000
  25. Modulation of sulfated proteoglycan synthesis by bovine aortic endothelial cells during migration.
    J Cell Biol. 1986 Mar;102(3):679-87 PMID: 3081523
  26. Morphoregulatory molecules.
    Biochemistry. 1988 May 17;27(10):3533-43 PMID: 3044445
  27. Syndecan and tenascin expression is induced by epithelial-mesenchymal interactions in embryonic tooth mesenchyme.
    J Cell Biol. 1989 May;108(5):1945-53 PMID: 2469682
  28. Angiogenic factors.
    Science. 1987 Jan 23;235(4787):442-7 PMID: 2432664
  29. Molecular cloning of syndecan, an integral membrane proteoglycan.
    J Cell Biol. 1989 Apr;108(4):1547-56 PMID: 2494194
  30. Regulation of cell adhesion receptors by transforming growth factor-beta. Concomitant regulation of integrins that share a common beta 1 subunit.
    J Biol Chem. 1989 Jan 5;264(1):380-8 PMID: 2491849
  31. Wound repair.
    Curr Opin Cell Biol. 1989 Oct;1(5):1000-8 PMID: 2697286
  32. Expression pattern of the FGF-related proto-oncogene int-2 suggests multiple roles in fetal development.
    Development. 1989 Jan;105(1):131-6 PMID: 2680421
  33. Proteoglycans in cell regulation.
    J Biol Chem. 1989 Aug 15;264(23):13369-72 PMID: 2668264
  34. Epithelial-mesenchymal interactions regulate the stage-specific expression of a cell surface proteoglycan, syndecan, in the developing kidney.
    Dev Biol. 1989 Aug;134(2):382-91 PMID: 2663574
  35. Reappearance of an embryonic pattern of fibronectin splicing during wound healing in the adult rat.
    J Cell Biol. 1989 Aug;109(2):903-14 PMID: 2760116
  36. Cell surface proteoglycan of mouse mammary epithelial cells is shed by cleavage of its matrix-binding ectodomain from its membrane-associated domain.
    J Cell Biol. 1987 Dec;105(6 Pt 2):3087-96 PMID: 3320062
  37. Ligand-affinity cloning and structure of a cell surface heparan sulfate proteoglycan that binds basic fibroblast growth factor.
    Proc Natl Acad Sci U S A. 1990 Sep;87(18):6985-9 PMID: 2144898
  38. Integrins and other cell adhesion molecules.
    FASEB J. 1990 Aug;4(11):2868-80 PMID: 2199285
  39. Sequence of human syndecan indicates a novel gene family of integral membrane proteoglycans.
    J Biol Chem. 1990 Apr 25;265(12):6884-9 PMID: 2324102
  40. Novel function for beta 1 integrins in keratinocyte cell-cell interactions.
    J Cell Biol. 1990 Mar;110(3):803-15 PMID: 1689734
  41. Fibronectin matrix deposition and fibronectin receptor expression in healing and normal skin.
    J Invest Dermatol. 1990 Jun;94(6 Suppl):128S-134S PMID: 2161886
  42. Cadherins: a molecular family important in selective cell-cell adhesion.
    Annu Rev Biochem. 1990;59:237-52 PMID: 2197976
  43. Polarized integrin mediates human keratinocyte adhesion to basal lamina.
    Proc Natl Acad Sci U S A. 1990 Sep;87(17):6888-92 PMID: 2395883
  44. Transient expression of a cell surface heparan sulfate proteoglycan (syndecan) during limb development.
    Dev Biol. 1990 Jul;140(1):83-92 PMID: 2358126
  45. Use of avidin-biotin-peroxidase complex (ABC) in immunoperoxidase techniques: a comparison between ABC and unlabeled antibody (PAP) procedures.
    J Histochem Cytochem. 1981 Apr;29(4):577-80 PMID: 6166661
  46. Basement membrane components in healing rabbit corneal epithelial wounds: immunofluorescence and ultrastructural studies.
    J Cell Biol. 1984 Jan;98(1):128-38 PMID: 6368566
  47. A cell-surface molecule involved in organ-specific homing of lymphocytes.
    Nature. 1983 Jul 7-13;304(5921):30-4 PMID: 6866086
  48. Detection of basement membrane zone antigens during epidermal wound healing in pigs.
    J Invest Dermatol. 1981 Aug;77(2):240-3 PMID: 7024426
  49. Effects of cytochalasins B and D and colchicine on migration of the corneal epithelium.
    Invest Ophthalmol Vis Sci. 1982 May;22(5):633-42 PMID: 7200475
  50. Migrating epidermis produces AB2 collagen and requires continual collagen synthesis for movement.
    Nature. 1979 Jan 18;277(5693):229-32 PMID: 551251
  51. Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease.
    Biochemistry. 1979 Nov 27;18(24):5294-9 PMID: 518835
  52. Inability of colchicine to inhibit newt epidermal cell migration or prevent concanavalin A-mediated inhibition of migration. Studies in vivo.
    Exp Cell Res. 1978 Oct 1;116(1):15-9 PMID: 699988
  53. Steroid-induced epithelial-fibroblastic conversion associated with syndecan suppression in S115 mouse mammary tumor cells.
    Cell Regul. 1991 Jan;2(1):1-11 PMID: 2007184
Article Info
Journal
The Journal of cell biology
Abbr.
J Cell Biol
ISSN
0021-9525
Published
1991-08-00
Pages
585-95
Language
English
Region
United States
NLM ID
0375356
PMCID
PMC2289093
Subset
IM
Grants
NIDCR NIH HHS · DE09399-01 · United States
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