Molecular Control of the Hyaluronan Biosynthesis

REFERENCES

• Toole B.P., Wight T.N., Tammi M.I. Hyaluronan-cell interactions in cancer and vascular disease. J. Biol. Chem. 2002; 277: 4593–4596
   PubMed Web of Science ®Google Scholar
• Itano N., Sawai T., Yoshida M., Lenas P., Yamada Y., Imagawa M., Shinomura T., Hamaguchi M., Yoshida Y., Ohnuki Y., Miyauchi S., Spicer A.P., McDonald J.A., Kimata K. Three isoforms of mammalian hyaluronan synthases have distinct enzymatic properties. J. Biol. Chem. 1999; 274: 25085–25092
   PubMed Web of Science ®Google Scholar
• Tien J.Y., Spicer A.P. Three vertebrate hyaluronan synthases are expressed during mouse development in distinct spatial and temporal patterns. Dev. Dyn. 2005; 233: 130–141
   PubMed Web of Science ®Google Scholar
• Turley E.A., Noble P.W., Bourguignon L.Y.W. Signaling properties of hyaluronan receptors. J. Biol. Chem. 2002; 277: 4589–4592
   PubMed Web of Science ®Google Scholar
• Cuff C.A., Kothapalli D., Azonobi I., Chun S., Zhang Y., Belkin R., Yeh C., Secreto A., Assoian R.K., Rader D.J., Pure E. The adhesion receptor CD44 promotes atherosclerosis by mediating inflammatory cell recruitment and vascular cell activation. J. Clin. Invest. 2001; 108: 1031–1040
   PubMed Web of Science ®Google Scholar
• Nedvetzki S., Gonen E., Assayag N., Reich R., Williams R.O., Thurmond R.L., Huang J., Neudecker B.A., Wang F., Turley E.A., Naor D. RHAMM, a receptor for hyaluronan-mediated motility, compensates for CD44 in inflamed CD44-knockout mice: a different interpretation of redundancy. Proc. Natl. Acad. Sci. USA 2004; 101: 18081–18086
   PubMed Web of Science ®Google Scholar
• Jackson D.G. The lymphatics revisited: new perspectives from the hyaluronan receptor LYVE-1. Trends Cardiovasc. Med. 2003; 13: 1–7
   PubMed Web of Science ®Google Scholar
• Harris E.N., Kyosseva S.V., Weigel J.A., Weigel P.H. Expression, processing, and glycosaminoglycan binding activity of the recombinant human 315-kDa hyaluronic acid receptor for endocytosis (HARE). J. Biol. Chem. 2007; 282: 2785–9277
   PubMed Web of Science ®Google Scholar
• Jiang D., Liang J., Fan J, Yu S., Chen S., Luo Y., Prestwich G.D., Mascarenhas M.M., Garg H.G., Quinn D.A., Homer R.J., Goldstein D.R., Bucala R., Lee P.J., Medzhitov R., Noble P W. Regulation of lung injury and repair by Toll-like receptors and hyaluronan. Nat. Med. 2005; 11: 1173–1179
   PubMed Web of Science ®Google Scholar
• de la Motte C.A., Hascall V.C., Drazba J., Bandyopadhyay S.K., Strong S.A. Mononuclear leukocytes bind to specific hyaluronan structures on colon mucosal smooth muscle cells treated with polyinosinic acid:polycytidylic acid: inter-alpha-trypsin inhibitor is crucial to structure and function. Am. J. Pathol. 2003; 163: 121–133
   PubMed Web of Science ®Google Scholar
• Majors A.K., Austin R.C., de la Motte C.A., Pyeritz R.E., Hascall V.C., Kessler S.P., Sen G., Strong S.A. Endoplasmic reticulum stress induces hyaluronan deposition and leukocyte adhesion. J. Biol. Chem. 2003; 278: 47223–47231
   PubMed Web of Science ®Google Scholar
• Hascall V.C., Majors A.K., De La Motte C.A., Evanko S.P., Wang A., Drazba J.A., Strong S.A., Wight T.N. Intracellular hyaluronan: a new frontier for inflammation?. Biochim. Biophys. Acta. 2004; 1673: 3–12
   PubMed Web of Science ®Google Scholar
• Heldin P. Importance of hyaluronan biosynthesis and degradation in cell differentiation and tumor formation. Braz. J. Med. Biol. Res. 2003; 36: 967–973
   PubMed Web of Science ®Google Scholar
• Riessen R., Wight T.N., Pastore C., Henley C., Isner J.M. Distribution of hyaluronan during extracellular matrix remodeling in human restenotic arteries and balloon-injured rat carotid arteries. Circulation 1996; 93: 1141–1147
   PubMed Web of Science ®Google Scholar
• Tzircotis G., Thorne R.F., Isacke C.M. Chemotaxis towards hyaluronan is dependent on CD44 expression and modulated by cell type variation in CD44-hyaluronan binding. J. Cell Sci. 2005; 118: 5119–5128
   PubMed Web of Science ®Google Scholar
• Chai S., Chai Q., Danielsen C.C., Hjorth P., Nyengaard J.R., Ledet T., Yamaguchi Y., Rasmussen L.M., Wogensen L. Overexpression of hyaluronan in the tunica media promotes the development of atherosclerosis. Circ. Res. 2005; 96: 583–591
   PubMed Web of Science ®Google Scholar
• Vigetti D., Moretto P., Viola M., Genasetti A., Rizzi M., Karousou E., Pallotti F., De Luca G., Passi A. Matrix metalloproteinase 2 and tissue inhibitors of metalloproteinases regulate human aortic smooth muscle cell migration during in vitro aging. FASEB J 2006; 20: 1118–1130
   PubMed Web of Science ®Google Scholar
• Vigetti D., Viola M., Karousou E., Rizzi M., Moretto P., Genasetti A., Clerici M., Hascall V.C., De Luca G., Passi A. Hyaluronan-CD44-ERK1/2 regulate human aortic smooth muscle cell motility during aging. J. Biol. Chem. 2008; 263: 4448–4458
   Web of Science ®Google Scholar
• Ge X., Penney L. C., van de Rijn I., Tanner M. E. Active site residues and mechanism of UDP-glucose dehydrogenase. Eur. J. Biochem. 2004; 271: 14–22
   PubMedGoogle Scholar
• Iozzo R. V., San Antonio J. D. Heparan sulfate proteoglycans: heavy hitters in the angiogenesis arena. J. Clin. Investig. 2001; 108: 349–355
   PubMed Web of Science ®Google Scholar
• Selva E.M., Perrimon N. Role of heparan sulfate proteoglycans in cell signaling and cancer. Adv. Cancer Res. 2001; 83: 67–80
   PubMed Web of Science ®Google Scholar
• Princivalle M., de Agostini A. Developmental roles of heparan sulfate proteoglycans: a comparative review in Drosophila, mouse and human. Int. J. Dev. Biol. 2002; 46: 267–278
   PubMed Web of Science ®Google Scholar
• Hacker U., Lin X., Perrimon N. The Drosophila sugarless gene modulates Wingless signaling and encodes an enzyme involved in polysaccharide biosynthesis. Development 1997; 124: 3565–3573
   PubMed Web of Science ®Google Scholar
• Hwang H.Y., Horvitz H.R. The Caenorhabditis elegans vulval morphogenesis gene sqv-4 encodes a UDP-glucose dehydrogenase that is temporally and spatially regulated. Proc. Natl. Acad. Sci. USA 2002; 99: 14224–14229
   PubMed Web of Science ®Google Scholar
• Hwang H.Y., Olson S.K., Esko J.D., Horvitz H.R. Caenorhabditis elegans early embryogenesis and vulval morphogenesis require chondroitin biosynthesis. Nature 2003; 423: 439–443
   PubMed Web of Science ®Google Scholar
• Walsh E.C., Stainier D.Y. UDP-glucose dehydrogenase required for cardiac valve formation in zebrafish. Science 2001; 293: 1670–1673
   PubMed Web of Science ®Google Scholar
• Garcia-Garcia M. J., Anderson K. V. Essential role of glycosaminoglycans in Fgf signaling during mouse gastrulation. Cell 2003; 114: 727–737
   PubMed Web of Science ®Google Scholar
• Galli A., Roure A., Zeller R., Dono R. Glypican 4 modulates FGF signalling and regulates dorsoventral forebrain patterning in Xenopus embryos. Development 2003; 130: 4919–4929
   PubMed Web of Science ®Google Scholar
• Latinkic B.V., Mercurio S., Bennett B., Hirst E.M., Xu Q., Lau L.F., Mohun T.J., Smith J.C. Xenopus Cyr61 regulates gastrulation movements and modulates Wnt signalling. Development 2003; 130: 2429–2441
   PubMed Web of Science ®Google Scholar
• Sander V., Mullegger J., Lepperdinger G. Xenopus brevican is expressed in the notochord and the brain during early embryogenesis. Mech. Dev. 2001; 102: 251–253
   PubMed Web of Science ®Google Scholar
• Anderson R.B., Walz A., Holt C.E., Key B. Chondroitin sulfates modulate axon guidance in embryonic Xenopus brain. Dev. Biol. 1998; 202: 235–243
   PubMed Web of Science ®Google Scholar
• Somasekhar T., Nordlander R.H. Selective early innervation of a subset of epidermal cells in Xenopus may be mediated by chondroitin sulfate proteoglycans. Brain Res. Dev. Brain Res. 1997; 99: 208–215
   PubMedGoogle Scholar
• Grunz H., Tacke L. Extracellular matrix components prevent neural differentiation of disaggregated Xenopus ectoderm cells. Cell Differ. Dev. 1990; 32: 117–123
   PubMedGoogle Scholar
• Mullegger J., Lepperdinger G. Hyaluronan is an abundant constituent of the extracellular matrix of Xenopus embryos. Mol. Reprod. Dev. 2002; 61: 312–316
   PubMed Web of Science ®Google Scholar
• Koprunner M., Mullegger J., Lepperdinger G. Synthesis of hyaluronan of distinctly different chain length is regulated by differential expression of Xhas1 and 2 during early development of Xenopus laevis. Mech. Dev. 2000; 90: 275–278
   PubMed Web of Science ®Google Scholar
• Haddon C. M., Lewis J. H. Hyaluronan as a propellant for epithelial movement: the development of semicircular canals in the inner ear of Xenopus. Development 1991; 112: 541–550
   PubMed Web of Science ®Google Scholar
• Vigetti D., Ori M., Viola M., Genasetti A., Karousou E., Rizzi M., Pallotti F., Nardi I., Hascall V.C., De Luca G., Passi A. Molecular cloning and characterization of UDP-glucose dehydrogenase from the amphibian xenopus laevis and its involvement in hyaluronan synthesis. J. Biol. Chem. 2006; 281: 8254–8263
   PubMed Web of Science ®Google Scholar
• Vigetti D., Viola M., Gornati R., Ori M., Nardi I., Passi A., De Luca G., Bernardini G. Molecular cloning, genomic organization and developmental expression of the Xenopus laevis hyaluronan synthase 3. Matrix Biol. 2003; 22: 511–517
   PubMed Web of Science ®Google Scholar
• Goentzel B.J., Weigel P.H., Steinberg R.A. Recombinant human hyaluronan synthase 3 is phosphorylated in mammalian cells. Biochem. J. 2006; 396: 347–354
   PubMed Web of Science ®Google Scholar
• Li L., Asteriou T., Bernert B., Heldin C.H., Heldin P. Growth factor regulation of hyaluronan synthesis and degradation in human dermal fibroblasts: importance of hyaluronan for the mitogenic response of PDGF-BB. Biochem. J. 2007; 404: 327–336
   PubMed Web of Science ®Google Scholar