The effect of basic fibroblast growth factor on regeneration in a surgical wound model of rat submandibular glands

Fumitaka Kobayashi , Kenichi Matsuzaka , Takashi Inoue

International Journal of Oral Science ›› 2015, Vol. 7 ›› Issue (1) : 16 -23.

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International Journal of Oral Science ›› 2015, Vol. 7 ›› Issue (1) : 16 -23. DOI: 10.1038/ijos.2015.36
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The effect of basic fibroblast growth factor on regeneration in a surgical wound model of rat submandibular glands

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Abstract

Collagen gel containing basic fibroblast growth factor could assist the regeneration of submandibular glands after damage during surgery. The slow healing of these large salivary glands, which lie beneath the floor of the mouth, causes difficulties with speaking, swallowing and digestion, and an increased susceptibility to oral infection. These problems can significantly impair a patient's quality of life. Fumitaka Kobayashi at Tokyo Dental College and co-workers explored the healing potential of basic fibroblast growth factor in collagen gel using rats that had been wounded to model surgical damage. They also monitored the proliferation and development of the specific types of cell involved in repairing the wounded tissue. Treating the wounds using collagen containing growth factor accelerated and improved healing to a greater extent than using collagen gel alone.

Keywords

animal model / basic fibroblast growth factor / collagen / immunohistochemistry / salivary gland / wound healing

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Fumitaka Kobayashi, Kenichi Matsuzaka, Takashi Inoue. The effect of basic fibroblast growth factor on regeneration in a surgical wound model of rat submandibular glands. International Journal of Oral Science, 2015, 7(1): 16-23 DOI:10.1038/ijos.2015.36

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References

[1]

Atkinson JC, Fox PC. Salivary gland dysfunction. Clin Geriatr Med, 1992, 8(3): 499-511.

[2]

Fox PC. Acquired salivary dysfunction. Drugs and radiation. Ann N Y Acad Sci, 1998, 842: 132-137.

[3]

Ship JA, Pillemer SR, Baum BJ. Xerostomia and the geriatric patient. J Am Geriatr Soc, 2002, 50(3): 535-543.

[4]

Magee DF. Salivary gland. Physiology and biophysics, 1965 Philadelphia, London

[5]

Carlson E, Ord R. Textbook and color atlas of salivary gland pathology: diagnosis and management, 2008 Hoboken

[6]

Provenza DV. Oral histology inheritance and development, 1964 Philadelphia, Montreal

[7]

Vissink A, Burlage FR, Spijkervet FK. Prevention and treatment of the consequences of head and neck radiotherapy. Crit Rev Oral Biol Med, 2003, 14(3): 213-225.

[8]

Vissink A, Jansma J, Spijkervet FK. Oral sequelae of head and neck radiotherapy. Crit Rev Oral Biol Med, 2003, 14(3): 199-212.

[9]

Takahashi S, Schoch E, Walker NI. Origin of acinar cell regeneration after atrophy of the rat parotid induced by duct obstruction. Int J Exp Pathol, 1998, 79(5): 293-301.

[10]

Man YG, Ball WD, Marchetti L. Contributions of intercalated duct cells to the normal parenchyma of submandibular glands of adult rats. Anat Rec, 2001, 263(2): 202-214.

[11]

Matsubara H, Kajiyama M. [An experimental study of wound healing after partial extirpation of Wistar rat submandibular gland.]. Kyushu-Shika-Gakkai-zasshi, 1992, 46(6): 818-831.

[12]

Parry DAD, Creamer LK. Fibrous proteins: scientific, industrial and medical aspects, 1980 Amsterdam

[13]

Gospodarowicz D, Greenburg G, Birdwell CR. Determination of cellular shape by the extracellular matrix and its correlation with the control of cellular growth. Cancer Res, 1978, 38(11 Pt 2): 4155-4171.

[14]

Wicha MS, Liotta LA, Garbisa S. Basement membrane collagen requirements for attachment and growth of mammary epithelium. Exp Cell Res, 1979, 124(1): 181-190.

[15]

Murray JC, Stingl G, Kleinman HK. Epidermal cells adhere preferentially to type IV (basement membrane) collagen. J Cell Biol, 1979, 80(1): 197-202.

[16]

Sattler CA, Michalopoulos G, Sattler GL. Ultrastructure of adult rat hepatocytes cultured on floating collagen membranes. Cancer Res, 1978, 38(6): 1539-1549.

[17]

Auger FA, Rouabhia M, Goulet F. Tissue-engineered human skin substitutes developed from collagen-populated hydrated gels: clinical and fundamental applications. Med Biol Eng Comput, 1998, 36(6): 801-812.

[18]

Yang W, Both SK, van Osch GJ. Performance of different three-dimensional scaffolds for in vivo endochondral bone generation. Eur Cell Mater, 2014, 27: 350-364.

[19]

Bornstein P, Traub W, Neurath H, Hill R. The chemistry and biology of collagen//. The proteins, 1979 Amsterdam 411-632.

[20]

Yoneda T, Imamoto A, Sakuda M. [Primary culture of mouse submandibular gland epithelial cells embedded in collagen gel matrix.]. Jpn J Oral Biol, 1986, 28: 12-18.

[21]

Rifkin DB, Moscatelli D. Recent developments in the cell biology of basic fibroblast growth factor. J Cell Biol, 1989, 109(1): 1-6.

[22]

Cuevas P, Burgos J, Baird A. Basic fibroblast growth factor (FGF) promotes cartilage repair in vivo. Biochem Biophys Res Commun, 1988, 156(2): 611-618.

[23]

Mazué G, Bertolero F, Jacob C. Preclinical and clinical studies with recombinant human basic fibroblast growth factor. Ann N Y Acad Sci, 1991, 638: 329-340.

[24]

Hoppenreijs VP, Pels E, Vrensen GF. Basic fibroblast growth factor stimulates corneal endothelial cell growth and endothelial wound healing of human corneas. Invest Ophthalmol Vis Sci, 1994, 35(3): 931-944.

[25]

Fina M, Baird A, Ryan A. Direct application of basic fibroblast growth factor improves tympanic membrane perforation healing. Laryngoscope, 1993, 103(7): 804-809.

[26]

Thula TT, Schultz G, Tran-Son-Tay R. Effects of EGF and bFGF on irradiated parotid glands. Ann Biomed Eng, 2005, 33(5): 685-695.

[27]

Cotrim AP, Sowers A, Mitchell JB. Prevention of irradiation-induced salivary hypofunction by microvessel protection in mouse salivary glands. Mol Ther, 2007, 15(12): 2101-2106.

[28]

Kojima T, Kanemaru S, Hirano S. The protective efficacy of basic fibroblast growth factor in radiation-induced salivary gland dysfunction in mice. Laryngoscope, 2011, 121(9): 1870-1875.

[29]

Ishii Y, Fujita T, Okubo N. Effect of basic fibroblast growth factor (FGF-2) in combination with beta tricalcium phosphate on root coverage in dog. Acta Odontol Scand, 2013, 71(2): 325-332.

[30]

Furuya H, Tabata Y, Kaneko K. Bone regeneration for murine femur fracture by gelatin hydrogels incorporating basic fibroblast growth factor with different release profiles. Tissue Eng Part A, 2014, 20(9/10): 1531-1541.

[31]

Hiramatsu Y, Kagami H, Horie K. Effects of basic fibroblast growth factor on cultured rat and human submandibular salivary gland cells. Arch Oral Biol, 2000, 45(7): 593-599.

[32]

Lee EY, Xia Y, Kim WS. Hypoxia-enhanced wound-healing function of adipose-derived stem cells: increase in stem cell proliferation and up-regulation of VEGF and bFGF. Wound Repair Regen, 2009, 17(4): 540-547.

[33]

Ihrler S, Zietz C, Sendelhofert A. A morphogenetic concept of salivary duct regeneration and metaplasia. Virchows Arch, 2002, 440(5): 519-526.

[34]

Matsuzaki T, Suzuki T, Koyama H. Aquaporin-5 (AQP5), a water channel protein, in the rat salivary and lacrimal glands: immunolocalization and effect of secretory stimulation. Cell Tissue Res, 1999, 295(3): 513-521.

[35]

Ma T, Song Y, Gillespie A. Defective secretion of saliva in transgenic mice lacking aquaporin-5 water channels. J Biol Chem, 1999, 274(29): 20071-20074.

[36]

Cotroneo E, Proctor GB, Paterson KL. Early markers of regeneration following ductal ligation in rat submandibular gland. Cell Tissue Res, 2008, 332(2): 227-235.

[37]

Nanduri LS, Maimets M, Pringle SA. Regeneration of irradiated salivary glands with stem cell marker expressing cells. Radiother Oncol, 2011, 99(3): 367-372.

[38]

Lombaert IM, Brunsting JF, Wierenga PK. Rescue of salivary gland function after stem cell transplantation in irradiated glands. PLoS One, 2008, 3(4): e2063.

[39]

Petrakova OS, Terskikh VV, Chernioglo ES. Comparative analysis reveals similarities between cultured submandibular salivary gland cells and liver progenitor cells. Springerplus, 2014, 3: 183.

[40]

Okumura K, Nakamura K, Hisatomi Y. Salivary gland progenitor cells induced by duct ligation differentiate into hepatic and pancreatic lineages. Hepatology, 2003, 38(1): 104-113.

[41]

Matsumoto S, Okumura K, Ogata A. Isolation of tissue progenitor cells from duct-ligated salivary glands of swine. Cloning Stem Cells, 2007, 9(2): 176-190.

[42]

Takahashi S, Kohgo T, Nakamura S. Biological behavior of myoepithelial cells in the regeneration of rat atrophied sublingual glands following release from duct ligation. J Mol Histol, 2005, 36(5): 373-379.

[43]

Warburton MJ, Ormerod EJ, Monaghan P. Characterization of a myoepithelial cell line derived from a neonatal rat mammary gland. J Cell Biol, 1981, 91(3 Pt 1): 827-836.

[44]

Warburton MJ, Ferns SA, Rudland PS. Enhanced synthesis of basement membrane proteins during the differentiation of rat mammary tumour epithelial cells into myoepithelial-like cells in vitro. Exp Cell Res, 1982, 137(2): 373-380.

[45]

Aumailley M, Timpl R, Sonnenberg A. Antibody to integrin alpha 6 subunit specifically inhibits cell-binding to laminin fragment 8. Exp Cell Res, 1990, 188(1): 55-60.

[46]

Okumura N, Takimoto K, Okada M. C6 glioma cells produce basic fibroblast growth factor that can stimulate their own proliferation. J Biochem, 1989, 106(5): 904-909.

[47]

Haimovitz-Friedman A, Balaban N, McLoughlin M. Protein kinase C mediates basic fibroblast growth factor protection of endothelial cells against radiation-induced apoptosis. Cancer Res, 1994, 54(10): 2591-2597.

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