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The inhibition of glycosaminoglycan incorporation influences the cell proliferation and cytodifferentiation in cultured embryonic mouse molars

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Abstract

The extracellular matrix (ECM) contains a variety of complex macromolecules including proteoglycans (PGs) and glycosaminoglycans (GAGs). PG consists of a protein core with covalently attached carbohydrate side chains called GAGs. Several PGs, including versican, biglycan, decorin and syndecan are involved in odontogenesis while the role of GAGs in those PGs in this process remains unclarified. The purpose of this study was to investigate the influence of GAGs on tooth development. The mandibular first molars at early bell stage were cultivated with or without 4-methylumbelliferyl-β-d-xyloside (Xyl-MU). The cultured tooth germs were metabolically labelled with [35S] Na2SO4, then PGs in tooth germs and cultured medium were extracted separately and analyzed by gel filtration. Morphological changes were evaluated on days 2, 4, 6, and histological changes were examined by hematoxylin-eosin (HE) staining and transmission electron microscope (TEM). Related proteins and genes of cytodifferentiation were further examined by immunohistochemistry (IHC) and quantitive real-time PCR (qPCR) respectively. Meanwhile, BrdU incorporation assay was used to explore the effect of Xyl-MU on the cell proliferation of cultured tooth germs. The results demonstrated that the incorporation of GAGs to PGs in cultured tooth germs was heavily inhibited by Xyl-MU. Accompanied by the inhibition of GAGs incorporation, Xyl-MU altered tooth morphogenesis and delayed the differentiation of ameloblasts and odontoblasts. Proliferation of inner enamel epithelium (IEE) was also inhibited. Therefore, we draw a conclusion that the inhibition of GAGs incorporation influences the cell proliferation and cytodifferentiation in cultured embryonic mouse molars.

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References

  • Berendsen AD, Fisher LW, Kilts TM, Owens RT, Robey PG, Gutkind JS et al (2011) Modulation of canonical wnt signaling by the extracellular matrix component biglycan. Proc Natl Acad Sci USA 108(41):17022–17027

    Article  CAS  Google Scholar 

  • Bishop JR, Schuksz M, Esko JD (2007) Heparan sulphate proteoglycans fine-tune mammalian physiology. Nature 446(7139):1030–1037

    Article  CAS  Google Scholar 

  • Carulli D, Laabs T, Geller HM, Fawcett JW (2005) Chondroitin sulfate proteoglycans in neural development and regeneration. Curr Opin Neurobiol 15(1):116–120

    Article  Google Scholar 

  • Chen XD, Fisher LW, Robey PG, Young MF (2004) The small leucine-rich proteoglycan biglycan modulates bmp-4-induced osteoblast differentiation. FASEB J 18(9):948–958

    Article  CAS  Google Scholar 

  • Cheng H, Caterson B, Yamauchi M (1999) Identification and immunolocalization of chondroitin sulfate proteoglycans in tooth cementum. Connect Tissue Res 40(1):37–47

    Article  CAS  Google Scholar 

  • Faassen AE, Mooradian DL, Tranquillo RT, Dickinson RB, Letourneau PC, Oegema TR et al (1993) Cell surface cd44-related chondroitin sulfate proteoglycan is required for transforming growth factor-beta-stimulated mouse melanoma cell motility and invasive behavior on type i collagen. J Cell Sci 105(2):501–511

    CAS  PubMed  Google Scholar 

  • Galbraith DB, Cutler LS, Kollar EJ (1992) The correlation of temporal regulation of glycosaminoglycan synthesis with morphogenetic events in mouse tooth development. Arch Oral Biol 37(8):623–628

    Article  CAS  Google Scholar 

  • Gao Z, Wang L, Wang F, Zhang C, Wang J, He J et al (2018) Expression of bmp2/4/7 during the odontogenesis of deciduous molars in miniature pig embryos. J Mol Histol 49(5):1–9

    Article  Google Scholar 

  • García­García MJ, Anderson KV (2003) Essential role of glycosaminoglycans in Fgf signaling during mouse gastrulation. Cell 114(6):727–737

    Article  Google Scholar 

  • Hamati HF, Britton EL, Carey DJ (1989) Inhibition of proteoglycan synthesis alters extracellular matrix deposition, proliferation, and cytoskeletal organization of rat aortic smooth muscle cells in culture. J Cell Biol 108(6):2495

    Article  CAS  Google Scholar 

  • He P, Zhang Y, Kim SO, Radlanski RJ, Butcher K, Schneider RA et al (2010) Ameloblast differentiation in the human developing tooth: effects of extracellular matrices. Matrix Biol 29(5):411–419

    Article  CAS  Google Scholar 

  • Inai T, Kukita T, Ohsaki Y, Nagata K, Kukita A, Kurisu K (1991) Immunohistochemical demonstration of amelogenin penetration toward the dental pulp in the early stages of ameloblast development in rat molar tooth germs. Anat Rec Adv Integr Anat Evolut Biol 229(2):259–270

    CAS  Google Scholar 

  • Jiang BZ, Yokohamatamaki T, Wang ZL, Obara N, Shibata S (2010) Expression, localisation and synthesis of versican by the enamel organ of developing mouse molar tooth germ: an in vivo and in vitro study. Arch Oral Biol 55(12):995–1006

    Article  CAS  Google Scholar 

  • Klein DJ, Brown DM, Moran A, Jr TRO, Platt JL (1989) Chondroitin sulfate proteoglycan synthesis and reutilization of beta-d-xyloside-initiated chondroitin/dermatan sulfate glycosaminoglycans in fetal kidney branching morphogenesis. Dev Biol 133(2):515–528

    Article  CAS  Google Scholar 

  • Lan Y, Jia S, Jiang R (2014) Molecular patterning of the mammalian dentition. Semin Cell Dev Biol 25–26:61–70

    Article  Google Scholar 

  • Landolt RM, Vaughan L, Winterhalter KH, Zimmermann DR (1995) Versican is selectively expressed in embryonic tissues that act as barriers to neural crest cell migration and axon outgrowth. Development 121(8):2303–2312

    CAS  PubMed  Google Scholar 

  • Lisi S, Peterkova R, Peterka M, Vonesch JL, Ruch JV, Lesot H et al (2003) Tooth morphogenesis and pattern of odontoblast differentiation. Connect Tissue Res 44(1):167–170

    Article  Google Scholar 

  • Liu L, Chen W, Li L, Xu F, Jiang B (2017) Inhibition of chondroitin sulfate glycosaminoglycans incorporation affected odontoblast differentiation in cultured embryonic mouse molars. J Mol Histol 48(5–6):1–9

    Article  Google Scholar 

  • Mark MP, Baker JR, Morrison K, Ruch JV (1990) Chondroitin sulfates in developing mouse tooth germs. Differentiation 43(1):37–50

    Article  CAS  Google Scholar 

  • Matsuura T, Duarte WR, Cheng H, Uzawa K, Yamauchi M (2001) Differential expression of decorin and biglycan genes during mouse tooth development. Matrix Biol 20(5–6):367–373

    Article  CAS  Google Scholar 

  • Melrose J, Isaacs MD, Smith SM, Hughes CE, Little CB, Caterson B et al (2012) Chondroitin sulphate and heparan sulphate sulphation motifs and their proteoglycans are involved in articular cartilage formation during human foetal knee joint development. Histochem Cell Biol 138(3):461–475

    Article  CAS  Google Scholar 

  • Milev P, Monnerie H, Popp S, Margolis RK, Margolis RU (1998) The core protein of the chondroitin sulfate proteoglycan phosphacan is a high-affinity ligand of fibroblast growth factor-2 and potentiates its mitogenic activity. J Biol Chem 273(34):21439–21442

    Article  CAS  Google Scholar 

  • Okahata S, Yamamoto R, Yamakoshi Y, Fukae M (2011) A large chondroitin sulfate proteoglycan, versican, in porcine predentin. J Oral Biosci 53(1):72–81

    Article  CAS  Google Scholar 

  • Rozario T, Desimone DW (2010) The extracellular matrix in development and morphogenesis: a dynamic view. Dev Biol 341(1):126–140

    Article  CAS  Google Scholar 

  • Ruch JV, Lesot H, Karcherdjuricic V, Meyer JM, Mark M (1983) Epithelial-mesenchymal interactions in tooth germs: mechanisms of differentiation. J Biol Buccale 11(3):173–193

    CAS  PubMed  Google Scholar 

  • Ruch JV, Lesot H, Bèguekirn C (1995) Odontoblast differentiation. Int J Dev Biol 39(1):51–68

    CAS  PubMed  Google Scholar 

  • Schwartz NB (1977) Regulation of chondroitin sulfate synthesis. Effect of beta-xylosides on synthesis of chondroitin sulfate proteoglycan, chondroitin sulfate chains, and core protein. J Biol Chem 252(18):6316–6321

    CAS  PubMed  Google Scholar 

  • Septier D, Hall RC, Embery G, Goldberg M (2001) Immunoelectron microscopic visualization of pro- and secreted forms of decorin and biglycan in the predentin and during dentin formation in the rat incisor. Calcif Tissue Int 69(1):38–45

    Article  CAS  Google Scholar 

  • Sherman LS, Back SA (2008) A ‘gag’ reflex prevents repair of the damaged cns. Trends Neurosci 31(1):44–52

    Article  CAS  Google Scholar 

  • Sotoodehnejadnematalahi F, Burke B (2013) Structure, function and regulation of versican: the most abundant type of proteoglycan in the extracellular matrix. Acta Med Iran 51(11):740–750

    CAS  PubMed  Google Scholar 

  • Takagaki K, Iwafune M, Kakizaki I, Ishido K, Kato Y, Endo M (2002) Cleavage of the xylosyl serine linkage between a core peptide and a glycosaminoglycan chain by cellulases. J Biol Chem 277(21):18397–18403

    Article  CAS  Google Scholar 

  • Tenãrio DM, Santos MF, Zorn TM (2003) Distribution of biglycan and decorin in rat dental tissue. Braz J Med Biol Res 36(8):1061–1065

    Article  Google Scholar 

  • Thesleff I (2003) Epithelial-mesenchymal signalling regulating tooth morphogenesis. J Cell Sci 116(9):1647–1648

    Article  CAS  Google Scholar 

  • Thesleff I, Nieminen P (1996) Tooth morphogenesis and cell differentiation. Curr Opin Cell Biol 8(6):844–850

    Article  CAS  Google Scholar 

  • Thesleff I, Jalkanen M, Vainio S, Bernfield M (1988) Cell surface proteoglycan expression correlates with epithelial-mesenchymal interaction during tooth morphogenesis. Dev Biol 129(2):565

    Article  CAS  Google Scholar 

  • Thompson HA, Spooner BS (1983) Proteoglycan and glycosaminoglycan synthesis in embryonic mouse salivary glands: effects of β-d-xyloside. an inhibitor of branching morphogenesis. J Cell Biol 96(5):1443–1450

    Article  CAS  Google Scholar 

  • Wang XP, Suomalainen M, Jorgez CJ, Matzuk MM, Wankell M, Werner S et al (2004) Modulation of activin/bone morphogenetic protein signaling by follistatin is required for the morphogenesis of mouse molar teeth. Dev Dyn 231(1):98–108

    Article  CAS  Google Scholar 

  • Wang H, Sun W, Ma J, Pan Y, Wang L, Zhang WB (2015) Biglycan mediates suture expansion osteogenesis via potentiation of wnt/β-catenin signaling. J Biomech 48(3):432–440

    Article  Google Scholar 

  • Wight TN (2002) Versican: a versatile extracellular matrix proteoglycan in cell biology. Curr Opin Cell Biol 14(5):617–623

    Article  CAS  Google Scholar 

  • Yamauchi S, Cheng H, Neame P, Caterson B, Yamauchi M (1997) Identification, partial characterization, and distribution of versican and link protein in bovine dental pulp. J Dent Res 76(11):1730–1736

    Article  CAS  Google Scholar 

  • Yan J, Stringer SE, Hamilton A, Charlton-Menys V, Götting C, Müller B et al (2011) Decorin gag synthesis and TGF-β signaling mediate ox-ldl-induced mineralization of human vascular smooth muscle cells. Arterioscler Thromb Vasc Biol 31(3):608–615

    Article  CAS  Google Scholar 

  • Yasuo T, Yamaguchi T, Kitaya K (2010) Progesterone induction of chondroitin sulfate proteoglycan aggrecan expression in human endometrial epithelial cells. J Steroid Biochem Mol Biol 122(4):159–163

    Article  CAS  Google Scholar 

Download references

Acknowledgements

Financial support for this study was provided by the Shanghai Science and Technology Commission Program (Nos. 15411965800) and Shanghai Municipal Commission of Health and Family Planning Program (Nos. 201740223).

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Correspondence to Beizhan Jiang.

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Jiang, B., Xu, F., Li, L. et al. The inhibition of glycosaminoglycan incorporation influences the cell proliferation and cytodifferentiation in cultured embryonic mouse molars. J Mol Hist 50, 11–19 (2019). https://doi.org/10.1007/s10735-018-9803-2

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  • DOI: https://doi.org/10.1007/s10735-018-9803-2

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