[1] Yamamura T. Differentiation of pulpal cells and inductive influences of various matrices with reference to pulpal wound healing[J]. J Dent Res, 1985, 64（spec）: 530-540.
[2] Nakashima M. Establishment of primary cultures of pulp cells from bovine permanent incisors[J]. Arch Oral Biol, 1991, 36(9): 655-663.
[3] Nakashima M, Nagasawa H, Yamada Y, et al. Regulatory role of transforming growth factor-β, bone morphogenetic protein-2, and protein-4 on gene expression of extracellular matrix proteins and differentiation of dental pulp cells[J]. Dev Biol, 1994, 162(1): 18-28.
[4] Kettunen P, Karavanova I, Thesleff I. Responsiveness of developing dental tissues to fibroblast growth factors: expression of splicing alternatives of FGFR1,‐2,‐3, and of FGFR4; and stimulation of cell proliferation by FGF‐2,‐4,‐8, and‐9[J]. Dev Genet, 1998, 22(4): 374-385.
[5] Buchaille R, Couble ML, Magloire H, et al. A substractive PCR-based cDNA library from human odontoblast cells: identification of novel genes expressed in tooth forming cells[J]. Matrix Biol, 2000, 19(5): 421-430.
[6] Yokose S, Kadokura H, Tajima Y, et al. Establishment and characterization of a culture system for enzymatically released rat dental pulp cells[J]. Calcif Tissue Int, 2000, 66(2): 139-144.
[7] About I, Bottero MJ, de Denato P, et al. Human Dentin Production in Vitro[J]. Exp Cell Res, 2000, 258(1): 33-41.
[8] Gronthos S, Mankani M, Brahim J, et al. Postnatal human dental pulp stem cells (DPSCs) in vitro and in vivo[J]. Proc Nat Acad Sci USA, 2000, 97(25): 13625-13630.
[9] Huang GT, Yamaza T, Shea LD, et al. Stem/progenitor cell-mediated de novo regeneration of dental pulp with newly deposited continuous layer of dentin in an in vivo model[J]. Tissue Eng Part A, 2010, 16(2): 605-615.
[10] Torabinejad M, Watson TF, Pitt Ford TR. Sealing ability of a mineral trioxide aggregate when used as a root end filling material[J]. J Endod, 1993, 19(12): 591-595.
[11] Paranjpe A, Zhang H, Johnson JD. Effects of mineral trioxide aggregate on human dental pulp cells after pulp-capping procedures[J]. J Endod, 2010, 36(6): 1042-1047.
[12] Aeinehchi M, Eslami B, Ghanbariha M, et al. Mineral trioxide aggregate (MTA) and calcium hydroxide as pulp‐capping agents in human teeth: a preliminary report[J]. Int End J, 2003, 36(3): 225-231.
[13] Zhao W, Wang J, Zhai W, et al. The self-setting properties and in vitro bioactivity of tricalcium silicate[J]. Biomaterials, 2005, 26(31): 6113-6121.
[14 ] 林开利, 常江, 汪正. 多孔硅酸钙生物陶瓷的制备及体外活性和降解性研究[J]. 无机材料学报, 2005, 20(3): 692-698.
[15] Mathieu S, El-Battari A, Dejou J. Role of injured endothelial cells in the recruitment of human pulp cells[J]. Arch Oral Biol, 2005, 50(2): 109-113.
[16] Pierdomenico L, Bonsi L, Calvitti M, et al. Multipotent mesenchymal stem cells with immunosuppressive activity can be easily isolated from dental pulp[J]. Transplantation, 2005, 80(6): 836-842.
[17] Butler W T, Ritchie H. The nature and functional significance of dentin extracellular matrix proteins[J]. Int J Dev Biol, 1995, 39(1): 169-179.
[18] MacDougall M, Gu TT, Simmons D. Dentin matrix protein-1, a candidate gene for dentinogenesis imperfecta[J]. Connect Tissue Res, 1996, 35(1-4): 267-272.
[19] Narayanan K, Gajjeraman S, Ramachandran A, et al. Dentin matrix protein 1 regulates dentin sialophosphoprotein gene transcription during early odontoblast differentiation[J]. J Biol Chem 2006, 281(28): 19064-19071.
[20] Garimella R, Bi X, Anderson H C, et al. Nature of phosphate substrate as a major determinant of mineral type formed in matrix vesicle-mediated in vitro mineralization: An FTIR imaging study[J]. Bone, 2006, 38(6): 811-817. |