The sequential seeding of epithelial and mesenchymal cells for tissue-engineered tooth regeneration

Biomaterials

Volumn 28, Issue 4, 2007, Pages 680-689

  Honda, Masaki J ^a   Tsuchiya, Shuhei ^a   Sumita, Yoshinori ^a   Sagara, Hiroshi ^b   Ueda, Minoru ^a,c  

^a THE UNIVERSITY OF TOKYO   (Japan)

^b UNIVERSITY OF TOKYO   (Japan)

^c NAGOYA UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

Author keywords

Cell cell interaction; Postnatal tooth cells; Sequential seeding; TEM (transmission electron microscopy); Tooth morphology; Tooth tissue engineering

Indexed keywords

CELLS; ENZYME KINETICS; MORPHOLOGY; TISSUE; TISSUE CULTURE; TRANSMISSION ELECTRON MICROSCOPY;

CELL-CELL INTERACTION; POSTNATAL TOOTH CELLS; SEQUENTIAL SEEDING; TOOTH MORPHOLOGY;

DENTISTRY;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CELL INTERACTION; CELL TYPE; COMPARATIVE STUDY; CONTROLLED STUDY; ENZYME ACTIVITY; EPITHELIUM CELL; IN VIVO STUDY; MESENCHYME; MESENCHYME CELL; MOLAR TOOTH; NONHUMAN; PRIORITY JOURNAL; RAT; SWINE; TISSUE ENGINEERING; TISSUE REGENERATION; TOOTH DEVELOPMENT; TRANSMISSION ELECTRON MICROSCOPY;

ALKALINE PHOSPHATASE; ANIMALS; CELL DIFFERENTIATION; CELL PROLIFERATION; CELLS, CULTURED; COCULTURE TECHNIQUES; EPITHELIAL CELLS; MESODERM; MICROSCOPY, ELECTRON, TRANSMISSION; RATS; REGENERATION; SWINE; TIME FACTORS; TISSUE ENGINEERING; TOOTH;

SUIDAE;

EID: 33750482568     PISSN: 01429612     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.biomaterials.2006.09.039     Document Type: Article

References (29)

1. Young C.S., Terada S., Vacanti J.P., Honda M., Bartlett J.D., and Yelick P.C. Tissue engineering of complex tooth structures on biodegradable polymer scaffolds. J Dent Res 81 (2002) 695-700
2. Honda M.J., Ohara T., Sumita Y., Ogaeri T., Kagami H., and Ueda M. Preliminary study of tissue-engineered odontogenesis in the canine jaw. J Oral Maxillofac Surg 64 (2006) 283-289
3. Sumita Y., Honda M.J., Ohara T., Tsuchiya S., Sagara H., Kagami H., et al. Performance of collagen sponge as a 3-D scaffold for tooth-tissue engineering. Biomaterials 27 (2006) 3238-3248
4. Honda M.J., Shinohara Y., Sumita Y., Tonomura A., Kagami H., and Ueda M. Shear stress facilitates tissue-engineered odontogenesis. Bone 39 (2006) 125-133
5. Honda M.J., Sumita Y., Kagami H., and Ueda M. Histological and immunohistochemical studies of tissue engineered odontogenesis. Arch Histol Cytol 68 (2005) 89-101
6. Young C.S., Kim S.W., Qin C., Baba O., Butler W.T., Taylor R.R., et al. Developmental analysis and computer modelling of bioengineered teeth. Arch Oral Biol 50 (2005) 259-265
7. Ohazama A., Modino S.A., Miletich I., and Sharpe P.T. Stem-cell-based tissue engineering of murine teeth. J Dent Res 83 (2004) 518-522
8. Yamamoto H., Kim E.J., Cho S.W., and Jung H.S. Analysis of tooth formation by reaggregated dental mesenchyme from mouse embryo. J Electron Microsc (Tokyo) 52 (2003) 559-566
9. Ye L., Mishina Y., Chen D., Huang H., Dallas S.L., Dallas M.R., et al. Dmp1-deficient mice display severe defects in cartilage formation responsible for a chondrodysplasia-like phenotype. J Biol Chem 280 (2005) 6197-6203
10. Slavkin H.C., Snead M.L., Zeichner-David M., Jaskoll T.F., and Smith B.T. Concepts of epithelial-mesenchymal interactions during development: tooth and lung organogenesis. J Cell Biochem 26 (1984) 117-125
11. Kusu N., Laurikkala J., Imanishi M., Usui H., Konishi M., Miyake A., et al. Sclerostin is a novel secreted osteoclast-derived bone morphogenetic protein antagonist with unique ligand specificity. J Biol Chem 278 (2003) 24113-24117
12. Jernvall J., and Thesleff I. Reiterative signaling and patterning during mammalian tooth morphogenesis. Mech Dev 92 (2000) 19-29
13. Thesleff I., Lehtonen E., and Saxen L. Basement membrane formation in transfilter tooth culture and its relation to odontoblast differentiation. Differentiation 10 (1978) 71-79
14. Thesleff I., and Hurmerinta K. Tissue interactions in tooth development. Differentiation 18 (1981) 75-88
15. Hsu S.M., Raine L., and Fanger H. Use of avidin-biotin-peroxidase complex (ABC) in immunoperoxidase techniques: a comparison between ABC and unlabeled antibody (PAP) procedures. J Histochem Cytochem 29 (1981) 577-580
16. Chen J., Zhang Q., McCulloch C.A., and Sodek J. Immunohistochemical localization of bone sialoprotein in foetal porcine bone tissues: comparisons with secreted phosphoprotein 1 (SPP-1, osteopontin) and SPARC (osteonectin). Histochem J 23 (1991) 281-289
17. Chai Y., and Slavkin H.C. Prospects for tooth regeneration in the 21st century: a perspective. Microsc Res Tech 60 (2003) 469-479
18. Earthman J.C., Sheets C.G., Paquette J.M., Kaminishi R.M., Nordland W.P., Keim R.G., et al. Tissue engineering in dentistry. Clin Plast Surg 30 (2003) 621-639
19. Nakashima M., and Reddi A.H. The application of bone morphogenetic proteins to dental tissue engineering. Nat Biotechnol 21 (2003) 1025-1032
20. Pavasant P., Yongchaitrakul T., Pattamapun K., and Arksornnukit M. The synergistic effect of TGF-beta and 1,25-dihydroxyvitamin D3 on SPARC synthesis and alkaline phosphatase activity in human pulp fibroblasts. Arch Oral Biol 48 (2003) 717-722
21. Alliot-Licht B., Bluteau G., Magne D., Lopez-Cazaux S., Lieubeau B., Daculsi G., et al. Dexamethasone stimulates differentiation of odontoblast-like cells in human dental pulp cultures. Cell Tissue Res 321 (2005) 391-400
22. Shiba H., Nakanishi K., Rashid F., Mizuno N., Hino T., Ogawa T., et al. Proliferative ability and alkaline phosphatase activity with in vivo cellular aging in human pulp cells. J Endod 29 (2003) 9-11
23. Nuki K., and Bonting S.L. Quantitative histochemistry of the developing hamster tooth: alkaline phosphatase and lactic dehydrogenase. J Histochem Cytochem 9 (1961) 117-125
24. Yoshiki S., and Kurahashi Y. A light and electron microscopic study of alkaline phosphatase activity in the early stage of dentinogenesis in the young rat. Arch Oral Biol 16 (1971) 1143-1154
25. Thesleff I. Tooth morphogenesis. Adv Dent Res 9 (1995) 12
26. Hay E.D., and Dodson J.W. Secretion of collagen by corneal epithelium. I. Morphology of the collagenous products produced by isolated epithelia grown on frozen-killed lens. J Cell Biol 57 (1973) 190-213
27. Pierce G.B. The development of basement membranes of the mouse embryo. Dev Biol 13 (1966) 231-249
28. Banerjee S.D., Cohn R.H., and Bernfield M.R. Basal lamina of embryonic salivary epithelia. Production by the epithelium and role in maintaining lobular morphology. J Cell Biol 73 (1977) 445-463
29. Thesleff I. Role of the basement membrane in odontoblast differentiation. J Biol Buccale 6 (1978) 241-249