SEARCH

SEARCH BY CITATION

References

  • 1
    De Salegui M, Pigman W. The existence of an acid-active hyaluronidase in serum. Arch Biochem Biophys 1967;120:6067.
  • 2
    Afify AM, Stern M, Guntenhoner M, Stern R. Purification and characterization of human serum hyaluronidase. Arch Biochem Biophys 1993;305:434441.
  • 3
    Frost GI, Csoka AB, Wong T, Stern R. Purification, cloning, and expression of human plasma hyaluronidase. Biochem Biophys Res Commun 1997;236:1015.
  • 4
    Stern R, Jedrzejas MJ. Hyaluronidases: their genomics, structures, and mechanisms of action. Chem Rev 2006;106:818839.
  • 5
    Girish KS, Kemparaju K. The magic glue hyaluronan and its eraser hyaluronidase: a biological overview. Life Sci 2007;80:19211943.
  • 6
    Hofinger ES, Spickenreither M, Oschmann J, Bernhardt G, Rudolph R, Buschauer A. Recombinant human hyaluronidase Hyal-1: insect cells versus Escherichia coli as expression system and identification of low molecular weight inhibitors. Glycobiology 2007;17:444453.
  • 7
    Hofinger ES, Bernhardt G, Buschauer A. Kinetics of Hyal-1 and PH-20 hyaluronidases: comparison of minimal substrates and analysis of the transglycosylation reaction. Glycobiology 2007;17:963971.
  • 8
    Fiszer-Szafarz B. Hyaluronidase polymorphism detected by polyacrylamide gel electrophoresis. Application to hyaluronidases from bacteria, slime molds, bee and snake venoms, bovine testes, rat liver lysosomes, and human serum. Anal Biochem 1984;143:7681.
  • 9
    Aronson NN Jr, Davidson EA. Lysosomal Hyaluronidase. J Biol Chem 1965;240:PC3222PC3224.
  • 10
    Natowicz MR, Short MP, Wang Y, Dickersin GR, Gebhardt MC, Rosenthal DI, Sims KB, Rosenberg AE. Clinical and biochemical manifestations of hyaluronidase deficiency. N Engl J Med 1996;335:10291033.
  • 11
    Triggs-Raine B, Salo TJ, Zhang H, Wicklow BA, Natowicz MR. Mutations in HYAL1, a member of a tandemly distributed multigene family encoding disparate hyaluronidase activities, cause a newly described lysosomal disorder, mucopolysaccharidosis IX. Proc Natl Acad Sci U S A 1999;96:62966300.
  • 12
    Guntenhoner MW, Pogrel MA, Stern R. A substrate-gel assay for hyaluronidase activity. Matrix 1992;12:388396.
  • 13
    Gasingirwa MC, Thirion J, Mertens-Strijthagen J, Wattiaux-De Coninck S, Flamion B, Wattiaux R, Jadot M. Endocytosis of hyaluronidase-1 by the liver. Biochem J 2010;430:305313.
  • 14
    Wattiaux R, Wibo M, Baudhuin P. Influence of the injection of Triton WR1339 on the properties of rat liver lysosomes. In: de Reuck AVS, Cameron MP, editors. Lysosomes, Ciba Foundation Symposium. Boston, MA: Little Brown and Co; 1963, pp. 176196.
  • 15
    Ghosh P, Dahms NM, Kornfeld S. Mannose 6-phosphate receptors: new twists in the tale. Nat Rev Mol Cell Biol 2003;4:202212.
  • 16
    Braulke T, Bonifacino JS. Sorting of lysosomal proteins. Biochim Biophys Acta 2009;1793:605614.
  • 17
    Maynard Y, Baenziger JU. Oligosaccharide specific endocytosis by isolated rat hepatic reticuloendothelial cells. J Biol Chem 1981;256:80638068.
  • 18
    Shepherd VL, Konish MG, Stahl P. Dexamethasone increases expression of mannose receptors and decreases extracellular lysosomal enzyme accumulation in macrophages. J Biol Chem 1985;260:160164.
  • 19
    Elvevold K, Simon-Santamaria J, Hasvold H, McCourt P, Smedsrod B, Sorensen KK. Liver sinusoidal endothelial cells depend on mannose receptor-mediated recruitment of lysosomal enzymes for normal degradation capacity. Hepatology 2008;48:20072015.
  • 20
    Imundo L, Leduc CA, Guha S, Brown M, Perino G, Gushulak L, Triggs-Raine B, Chung WK. A complete deficiency of Hyaluronoglucosaminidase 1 (HYAL1) presenting as familial juvenile idiopathic arthritis. J Inherit Metab Dis 2011;34:10131022.
  • 21
    De Duve C, Pressman BC, Gianetto R, Wattiaux R, Appelmans F. Tissue fractionation studies. 6. Intracellular distribution patterns of enzymes in rat-liver tissue. Biochem J 1955;60:604617.
  • 22
    DeCourcy K, Storrie B. Osmotic swelling of endocytic compartments induced by internalized sucrose is restricted to mature lysosomes in cultured mammalian cells. Exp Cell Res 1991;192:5260.
  • 23
    Hamer I, Jadot M. Endolysosomal transport of newly-synthesized cathepsin D in a sucrose model of lysosomal storage. Exp Cell Res 2005;309:284295.
  • 24
    Csoka AB, Frost GI, Heng HH, Scherer SW, Mohapatra G, Stern R. The hyaluronidase gene HYAL1 maps to chromosome 3p21.2-p21.3 in human and 9 F1-F2 in mouse, a conserved candidate tumor suppressor locus. Genomics 1998;48:6370.
  • 25
    Piemonti L, Monti P, Allavena P, Leone BE, Caputo A, Di Carlo V. Glucocorticoids increase the endocytic activity of human dendritic cells. Int Immunol 1999;11:15191526.
  • 26
    Shepherd VL, Cowan HB, Abdolrasulnia R, Vick S. Dexamethasone blocks the interferon-gamma-mediated downregulation of the macrophage mannose receptor. Arch Biochem Biophys 1994;312:367374.
  • 27
    Qian M, Sleat DE, Zheng H, Moore D, Lobel P. Proteomics analysis of serum from mutant mice reveals lysosomal proteins selectively transported by each of the two mannose 6-phosphate receptors. Mol Cell Proteomics 2008;7:5870.
  • 28
    Sun P, Sleat DE, Lecocq M, Hayman AR, Jadot M, Lobel P. Acid phosphatase 5 is responsible for removing the mannose 6-phosphate recognition marker from lysosomal proteins. Proc Natl Acad Sci U S A 2008;105:1659016595.
  • 29
    Gelfman CM, Vogel P, Issa TM, Turner CA, Lee WS, Kornfeld S, Rice DS. Mice lacking alpha/beta subunits of GlcNAc-1-phosphotransferase exhibit growth retardation, retinal degeneration, and secretory cell lesions. Invest Ophthalmol Vis Sci 2007;48:52215228.
  • 30
    Sleat DE, Wang Y, Sohar I, Lackland H, Li Y, Li H, Zheng H, Lobel P. Identification and validation of mannose 6-phosphate glycoproteins in human plasma reveal a wide range of lysosomal and non-lysosomal proteins. Mol Cell Proteomics 2006;5:19421956.
  • 31
    Sleat DE, Lackland H, Wang Y, Sohar I, Xiao G, Li H, Lobel P. The human brain mannose 6-phosphate glycoproteome: a complex mixture composed of multiple isoforms of many soluble lysosomal proteins. Proteomics 2005;5:15201532.
  • 32
    Csoka AB, Frost GI, Wong T, Stern R. Purification and microsequencing of hyaluronidase isozymes from human urine. FEBS Lett 1997;417:307310.
  • 33
    Zhang L, Bharadwaj AG, Casper A, Barkley J, Barycki JJ, Simpson MA. Hyaluronidase activity of human Hyal1 requires active site acidic and tyrosine residues. J Biol Chem 2009;284:94339442.
  • 34
    Chao KL, Muthukumar L, Herzberg O. Structure of human hyaluronidase-1, a hyaluronan hydrolyzing enzyme involved in tumor growth and angiogenesis. Biochemistry 2007;46:69116920.
  • 35
    Arunachalam B, Phan UT, Geuze HJ, Cresswell P. Enzymatic reduction of disulfide bonds in lysosomes: characterization of a gamma-interferon-inducible lysosomal thiol reductase (GILT). Proc Natl Acad Sci U S A 2000;97:745750.
  • 36
    Sleat DE, Della Valle MC, Zheng H, Moore DF, Lobel P. The mannose 6-phosphate glycoprotein proteome. J Proteome Res 2008;7:30103021.
  • 37
    Hemming R, Martin DC, Slominski E, Nagy JI, Halayko AJ, Pind S, Triggs-Raine B. Mouse Hyal3 encodes a 45- to 56-kDa glycoprotein whose overexpression increases hyaluronidase 1 activity in cultured cells. Glycobiology 2008;18:280289.
  • 38
    Atmuri V, Martin DC, Hemming R, Gutsol A, Byers S, Sahebjam S, Thliveris JA, Mort JS, Carmona E, Anderson JE, Dakshinamurti S, Triggs-Raine B. Hyaluronidase 3 (HYAL3) knockout mice do not display evidence of hyaluronan accumulation. Matrix Biol 2008;27:653660.
  • 39
    Gushulak L, Hemming R, Martin D, Seyrantepe V, Pshezhetsky A, Triggs-Raine B. Hyaluronidase 1 and beta-hexosaminidase have redundant functions in hyaluronan and chondroitin sulfate degradation. J Biol Chem 2012;287:1668916697.
  • 40
    Jadot M, Dubois F, Wattiaux-De Coninck S, Wattiaux R. Supramolecular assemblies from lysosomal matrix proteins and complex lipids. Eur J Biochem 1997;249:862869.
  • 41
    Fiszer-Szafarz B, Czartoryska B, Tylki-Szymanska A. Serum hyaluronidase aberrations in metabolic and morphogenetic disorders. Glycoconj J 2005;22:395400.
  • 42
    Natowicz MR, Wang Y. Plasma hyaluronidase activity in mucolipidoses II and III: marked differences from other lysosomal enzymes. Am J Med Genet 1996;65:209212.
  • 43
    Harada H, Takahashi M. CD44-dependent intracellular and extracellular catabolism of hyaluronic acid by hyaluronidase-1 and -2. J Biol Chem 2007;282:55975607.
  • 44
    Andre B, Duterme C, Van Moer K, Mertens-Strijthagen J, Jadot M, Flamion B. Hyal2 is a glycosylphosphatidylinositol-anchored, lipid raft-associated hyaluronidase. Biochem Biophys Res Commun 2011;411:175179.
  • 45
    Haka AS, Grosheva I, Chiang E, Buxbaum AR, Baird BA, Pierini LM, Maxfield FR. Macrophages create an acidic extracellular hydrolytic compartment to digest aggregated lipoproteins. Mol Biol Cell 2009;20:49324940.
  • 46
    Esko JD, Kimata K, Lindahl U. Proteoglycans and sulfated glycosaminoglycans. In: Varki A, Cummings RD, Esko JD, Freeze HH, Stanley P, Bertozzi CR, Hart GW, Etzler ME, editors. Essentials of Glycobiology, 2 edn. New York: Cold Spring Harbor; 2009.
  • 47
    Martin DC, Atmuri V, Hemming RJ, Farley J, Mort JS, Byers S, Hombach-Klonisch S, Csoka AB, Stern R, Triggs-Raine BL. A mouse model of human mucopolysaccharidosis IX exhibits ostearthritis. Hum Mol Genet 2008;17:19041915.