Characteristics of high-molecular-weight hyaluronic acid as a brain-derived neurotrophic factor scaffold in periodontal tissue regeneration

Tissue Engineering - Part A

Volumn 17, Issue 7-8, 2011, Pages 955-967

  Takeda, Katsuhiro ^a   Sakai, Noriyuki ^a   Shiba, Hideki ^a   Nagahara, Takayoshi ^a   Fujita, Tsuyoshi ^a   Kajiya, Mikihito ^a   Iwata, Tomoyuki ^a   Matsuda, Shinji ^a   Kawahara, Kazuko ^a   Kawaguchi, Hiroyuki ^a   Kurihara, Hidemi ^a  

^a HIROSHIMA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

BONE; CELL CULTURE; ENZYME INHIBITION; LIGAMENTS; ORGANIC ACIDS;

ALVEOLAR BONES; ATELOCOLLAGEN; BOVINE COLLAGEN; BRAIN-DERIVED NEUROTROPHIC FACTORS; CLINICAL APPLICATION; GLYCOLIC ACIDS; HIGH MOLECULAR WEIGHT; HUMAN PERIODONTAL LIGAMENT CELLS; HYALURONIC ACIDS; IN-VITRO; MRNA EXPRESSION; PERIODONTAL TISSUE; POLY(LACTIC-CO-GLYCOLIC ACID); REGENERATIVE CAPACITY;

SCAFFOLDS (BIOLOGY);

BOVINAE; CANIS FAMILIARIS;

BRAIN DERIVED NEUROTROPHIC FACTOR; HYALURONIC ACID; TISSUE SCAFFOLD;

ANIMAL; ARTICLE; CATTLE; CELL ADHESION; CELL CULTURE; CHEMISTRY; CYTOLOGY; DRUG EFFECT; FLUORESCENCE MICROSCOPY; GENETICS; HUMAN; IMMUNOHISTOCHEMISTRY; MOLECULAR WEIGHT; PERIODONTIUM; PHYSIOLOGY; REGENERATION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION;

ANIMALS; BRAIN-DERIVED NEUROTROPHIC FACTOR; CATTLE; CELL ADHESION; CELLS, CULTURED; HUMANS; HYALURONIC ACID; IMMUNOHISTOCHEMISTRY; MICROSCOPY, FLUORESCENCE; MOLECULAR WEIGHT; PERIODONTIUM; REGENERATION; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; TISSUE SCAFFOLDS;

EID: 79952935665     PISSN: 19373341     EISSN: 1937335X     Source Type: Journal    
DOI: 10.1089/ten.tea.2010.0070     Document Type: Article

References (50)

1. Johnson, D., Lanahan, A., Buck, C.R., Sehagal, A., Morgan, C., Mercer, E., Bothwell, M., and Chao, M. Expression and structure of the human NGF receptor. Cell 47, 545, 1986.
2. Radeke, M.J., Misko, T.P., Hsu, C., Herzenberg, L.A., and Shooter, E.M. Gene transfer and molecular cloning of the rat nerve growth factor receptor. Nature 325, 593, 1987.
3. Barbacid, M. The Trk family of neurotrophin receptors. J Neurobiol 25, 1386, 1994.
4. Ebendal, T. Function and evolution in the NGF family and its receptors. J Neurosci Res 32, 461, 1992.
5. Takeda, K., Shiba, H., Mizuno, N., Hasegawa, N., Mouri, Y., Hirachi, A., Yoshino, H., Kawaguchi, H., and Kurihara, H. Brain-derived neurotrophic factor enhances periodontal tissue regeneration. Tissue Eng 11, 1618, 2005.
6. Kajiya, M., Shiba, H., Fujita, T., Ouhara, K., Takeda, K., Mizuno, N., Kawaguchi, H., Kitagawa, M., Takata, T., Tsuji, K., and Kurihara, H. Brain-derived neurotrophic factor stimulates bone/cementum-related protein gene expression in cementoblasts. J Biol Chem 283, 16259, 2008.
7. Kajiya, M., Shiba, H., Fujita, T., Takeda, K., Uchida, Y., Kawaguchi, H., Kitagawa, M., Takata, T., and Kurihara, H. Brain-derived neurotrophic factor protects cementoblasts from serum starvation-induced cell death. J Cell Physiol 221, 696, 2009.
8. Nakahashi, T., Fujimura, H., Altar, C.A., Li, J., Kambayashi, J., Tandon, N.N., and Sun, B. Vascular endothelial cells synthesize and secrete brain-derived neurotrophic factor. FEBS Lett 470, 113, 2000.
9. Nakanishi, T., Takahashi, K., Aoki, C., Nishikawa, K., Hattori, T., and Taniguchi, S. Expressions of nerve growth factor family neurotrophins in a mouse osteoblastic cell line. Biochem Biophys Res Commun 198, 891, 1994.
10. Kerschensteiner, M., Gallmeier, E., Behrens, L., Leal, V.V., Misgeld, T., Klinkert, W.E., Kolbeck, R., Hoppe, E., Oropeza-Wekerle, R.L., Bartke, I., Stadelmann, C., Lassmann, H., Wekerle, H., and Hohlfeld, R. Activated human T cells, B cells, and monocytes produce brain-derived neurotrophic factor in vitro and in inflammatory brain lesions: a neuroprotective role of inflammation? J Exp Med 189, 865, 1999.
11. Somerman, M.J., Ouyang, H.J., Berry, J.E., Saygin, N.E., Strayhorn, C.L., D'Errico, J.A., Hullinger, T., and Giannobile, W.V. Evolution of periodontal regeneration: from the roots' point of view. J Periodontal Res 34, 420, 1999.
12. Somerman, M.J., Young, M.F., Foster, R.A., Moehring, J.M., Imm, G., and Sauk, J.J. Characteristics of human periodontal ligament cells in vitro. Arch Oral Biol 35, 241, 1990.
13. McCulloch, C.A.G., and Bordin, S. Role of fibroblast subpopulations in periodontal physiology and pathology. J Periodontal Res 26, 144, 1991.
14. Nohutcu, R.M., McCauley, L.K., Koh, A.J., and Somerman, M.J. Expression of extracellular matrix proteins in human periodontal ligament cells during mineralization in vitro. J Periodontal 68, 320, 1997.
15. Taba, M., Jr., Jin, Q., Sugai, J.V., and Giannobile, W.V. Current concepts in periodontal bioengineering. Orthod Craniofac Res 8, 292, 2005.
16. Hardingham, T.E., and Fosang, A.J. Proteoglycans: many forms and many functions. FASEB J 6, 861, 1992.
17. Chen, W.Y., and Abatangelo, G. Functions of hyaluronan in wound repair. Wound Repair Regen 7, 79, 1999.
18. Goa, K.L., and Benfield, P. Hyaluronic acid. A review of its pharmacology and use as a surgical aid in ophthalmology, and its therapeutic potential in joint disease and wound healing. Drugs 47, 536, 1994.
19. Weigel, P.H., Fuller, G.M., and Le Boeuf, R.D. A model for the role of hyaluronic acid and fibrin in the early events during the inflammatory response and wound healing. J Theor Biol 119, 219, 1986.
20. Weigel, P.H., Hascall, V.C., and Tammi, M. Hyaluronan synthases. J Biol Chem 272, 13997, 1997.
21. Toole, B.P. Hyaluronan: from extracellular glue to pericellular cue. Nat Rev Cancer 4, 528, 2004.
22. Noble, P.W. Hyaluronan and its catabolic products in tissue injury and repair. Matrix Biol 21, 25, 2002.
23. David-Raoudi, M., Tranchepain, F., Deschrevel, B., Vincent, J.C., Bogdanowicz, P., Boumediene, K., and Pujol, J.P. Differential effects of hyaluronan and its fragments on fibroblasts: relation to wound healing. Wound Repair Regen 16, 274, 2008.
24. Kato, Y., Nakamura, S., and Nishimura, M. Beneficial actions of hyaluronan (HA) on arthritic joints: effects of molecular weight of HA on elasticity of cartilage matrix. Biorheology 43, 347, 2006.
25. Mitsui, Y., Gotoh, M., Nakama, K., Yamada, T., Higuchi, F., and Nagata, K. Hyaluronic acid inhibits mRNA expression of proinflammatory cytokines and cyclooxygenase-2/ prostaglandin E(2) production via CD44 in interleukin-1- stimulated subacromial synovial fibroblasts from patients with rotator cuff disease. J Orthop Res 26, 1032, 2008.
26. Aruffo, A., Stamenkovic, I., Melnick, M., Underhill, C.B., and Seed, B. CD44 is the principal cell surface receptor for hyaluronate. Cell 61, 1303, 1990.
27. Laurent, T.C., and Fraser, J.R. Hyaluronan. FASEB J 6, 2397, 1992.
28. Chen, W.Y., and Abatangelo, G. Functions of hyaluronan in wound repair. Wound Repair Regen 7, 79, 1999.
29. Puré, E., and Cuff, C.A. A crucial role for CD44 in inflammation. Trends Mol Med 7, 213, 2001.
30. Ponta, H., Sherman, L., and Herrlich, P.A. CD44: from adhesion molecules to signalling regulators. Nat Rev Mol Cell Biol 4, 33, 2003.
31. Polimeni, G., Xiropaidis, A.V., and Wikesjö, U.M. Biology and principles of periodontal wound healing/regeneration. Periodontol 2000 41, 30, 2006.
32. Pasquinelli, G., Orrico, C., Foroni, L., Bonafè, F., Carboni, M., Guarnieri, C., Raimondo, S., Penna, C., Geuna, S., Pagliaro, P., Freyrie, A., Stella, A., Caldarera, C.M., and Muscari, C. Mesenchymal stem cell interaction with a non-woven hyaluronan-based scaffold suitable for tissue repair. J Anat 213, 520, 2008.
33. West, D.C., and Kumar, S. The effect of hyaluronate and its oligosaccharides on endothelial cell proliferation and monolayer integrity. Exp Cell Res 183, 179, 1989.
34. Mast, B.A., Diegelmann, R.F., Krummel, T.M., and Cohen, I.K. Hyaluronic acid modulates proliferation, collagen and protein synthesis of cultured fetal fibroblasts. Matrix 13, 441, 1993.
35. Bodo, M., Pezzetti, F., Baroni, T., Carinci, F., Arena, N., Nicoletti, I., and Becchetti, E. Hyaluronic acid modulates growth, morphology and cytoskeleton in embryonic chick skin fibroblasts. Int J Dev Biol 37, 349, 1993.
36. Hehenberger, K., Kratz, G., Hansson, A., and Brismar, K. Fibroblasts derived from human chronic diabetic wounds have a decreased proliferation rate, which is recovered by the addition of heparin. J Dermatol Sci 16, 144, 1998.
37. Moon, S.O., Lee, J.H., and Kim, T.J. Changes in the expression of cmyc, RB and tyrosine-phosphorylated proteins during proliferation of NIH 3T3 cells induced by hyaluronic acid. Exp Mol Med 30, 29, 1998.
38. Wang, C.K., Ho, M.L., Wang, G.J., Chang, J.K., Chen, C.H., Fu, Y.C., and Fu, H.H. Controlled-release of rhBMP-2 carriers in the regeneration of osteonecrotic bone. Biomaterials 30, 4178, 2009.
39. Lu, H.H., Vo, J.M., Chin, H.S., Lin, J., Cozin, M., Tsay, R., Eisig, S., and Landesberg, R. Controlled delivery of plateletrich plasma-derived growth factors for bone formation. J Biomed Mater Res A 86, 1128, 2008.
40. Lesley, J., Schulte, R., and Hyman, R. Binding of hyaluronic acid to lymphoid cell lines is inhibited by monoclonal antibodies against Pgp-1. Exp Cell Res 187, 224, 1990.
41. Miyake, K., Underhill, C.B., Lesley, J., and Kincade, P.W. Hyaluronate can function as a cell adhesion molecule and CD44 participates in hyaluronate recognition. J Exp Med 172, 69, 1990.
42. Lee, J.Y., and Spicer, A.P. Hyaluronan: a multifunctional, megaDalton, stealth molecule. Curr Opin Cell Biol 12, 581, 2000.
43. Nakamura, H., Kenmotsu, S., Sakai, H., and Ozawa, H. Localization of CD44, the hyaluronate receptor, on the plasma membrane of osteocytes and osteoclasts in rat tibiae. Cell Tissue Res 280, 225, 1995.
44. Cieślik, M., Mertas, A., Morawska-Chochól, A., Sabat, D., Orlicki, R., Owczarek, A., Król, W., and Cieślik, T. The evaluation of the possibilities of using PLGA co-polymer and its composites with carbon fibers or hydroxyapatite in the bone tissue regeneration process-in vitro and in vivo examinations. Int J Mol Sci 10, 3224, 2009.
45. Taylor, M.S., Daniels, A.U., Andriano, K.P., and Heller, J. Six bioabsorbable polymers: in vitro acute toxicity of accumulated degradation products. J Appl Biomater 5, 151, 1994.
46. Klompmaker, J., Jansen, H.W., Veth, R.P., de Groot, J.H., Nijenhuis, A.J., and Pennings, A.J. Porous polymer implant for repair of meniscal lesions: a preliminary study in dogs. Biomaterials 12, 810, 1991.
47. Kawaguchi, H., Ogawa, T., Kurihara, H., and Nanci, A. Immunodetection of noncollagenous matrix proteins during periodontal tissue regeneration. J Periodontal Res 36, 205, 2001.
48. Nandasena, B.G., Suzuki, A., Aita, M., Kawano, Y., Nozawa-Inoue, K., and Maeda, T. Immunolocalization of aquaporin-1 in the mechanoreceptive Ruffini endings in the periodontal ligament. Brain Res 1157, 32, 2007.
49. Yamada, S., Terada, K., Ueno, Y., Sugiyama, T., Seno, M., and Kojima, I. Differentiation of adult hepatic stem-like cells into pancreatic endocrine cells. Cell Transplant 14, 647, 2005.
50. Yokoyama-Hayashi, K., Takahashi, T., Kakita, A., and Yamashina, S. Expression of PGP9.5 in ductal cells of the rat pancreas during development and regeneration: can it be a marker for pancreatic progenitor cells? Endocr J 49, 61, 2002.