Oral Cells and Tissues. Philias R. Garant. Читать онлайн. Newlib. NEWLIB.NET

Автор: Philias R. Garant
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apparatus. Curr Opin Cell Biol 1995; 7:530–535.

      193. Kreis TE, Pepperkok R. Coat proteins in intracellular membrane transport. Curr Opin Cell Biol 1994;6:533–537.

      194. Kreis TE, Lowe M, Pepperkok R. COPs regulating membrane traffic. Annu Rev Cell Biol 1995;11:677–706.

      195. Salama NR, Schekman RW. The role of coat proteins in the biosynthesis of secretory proteins. Curr Opin Cell Biol 1995; 7:536–543.

      196. Beckers CJ, Balch WE. Calcium and GTP: Essential components in vesicular trafficking between the endoplasmic reticulum and Golgi apparatus. J Cell Biol 1989;108:1245–1256.

      197. Terrian DM, White MK. Phylogenetic analysis of membrane trafficking proteins: A family reunion and secondary structure predictions. Eur J Cell Biol 1997;73:198–204.

      198. Wilson DW, Whiteheart SW, Wiedmann M, Brunner M, Rothman JE. A multisubunit particle implicated in membrane fusion. J Cell Biol 1992;117:531–538.

      199. Kelly RB. Pathways of protein secretion in eucaryotes. Science 1985;230:25–32.

      200. Kelly RB. Secretory granule and synaptic vesicle formation. Curr Opin Cell Biol 1991;3:654–660.

      201. Arvan P, Castle D. Protein sorting and secretion granule formation in regulated secretory cells. Trends Cell Biol 1992;2: 327–331.

      202. Bi GQ, Morris RL, Liao GC, Alderton JM, Scholey JM, Steinhardt RA. Kinesin- and myosin-driven steps of vesicle recruitment for Ca2+-regulated exocytosis. J Cell Biol 1997;138: 999–1008.

      203. Romagnoli P, Mancini G, Galeotti F, Francini E, Pierleoni P. The crown odontoblasts of rat molars from primary dentinogenesis to complete eruption. J Dent Res 1990;69:1857–1862.

      204. Bjorndal L, Darvann T, Thylstrup A. A quantitative light microscopic study of the odontoblast and subodontoblastic reactions to active and arrested enamel caries without cavitation. Caries Res 1998;32:59–69.

      205. Farges JC, Joffre A, Lesot H, Bleicher F, Magloire H. Immunocytochemical localization of fibronectin and a 165-kDa membrane protein in the odontoblast layer under initial carious lesions in man. Arch Oral Biol 1995;40:1023–1028.

      206. D’Souza RN, Bachman T, Baumgardner KR, Butler WT, Litz M. Characterization of cellular responses involved in reparative dentinogenesis in rat molars. J Dent Res 1995;74: 702–709.

      207. Tziafas D, Panagiotakopoulos N, Komnenou A. Immunolocalization of fibronectin during the early response of dog dental pulp to demineralized dentine or calcium hydroxide-containing cement. Arch Oral Biol 1995;40:23–31.

      208. Bègue-Kirn C, Smith AJ, Ruch JV, Wozney JM, Purchio A, Hartmann D, Lesot H. Effects of dentin proteins, transforming growth factor β1 (TGF-β1) and bone morphogenetic protein 2 (BMP2) on the differentiation of odontoblasts in vitro. Int J Dev Biol 1992;36:491–503.

      209. Nakashima M, Nagasawa H, Yamada Y, Reddi AH. Regulatory role of transforming growth factor-beta, bone morphogenetic protein-2, and protein-4 on gene expression of extracellular matrix proteins and differentiation of dental pulp cells. Dev Biol 1994;162:18–28.

      210. Nakashima M. Induction of dentin formation on canine amputated pulp by recombinant human bone morphogenetic proteins (BMP)-2 and -4. J Dent Res 1994;73:1515–1522.

      211. Gu K, Smoke RH, Rutherford RB. Expression of genes for bone morphogenetic proteins and receptors in human dental pulp. Arch Oral Biol 1996;41:919–923.

      212. Takeda K, Oida S, Goseki M, Iimura T, Maruoka Y, Amagasa T, Sasaki S. Expression of bone morphogenetic protein genes in the human dental pulp cells. Bone 1994;15:467–470.

      213. Lesot H, Bègue-Kirn C, Kubler MD, Meyer JM, Smith AJ, Cassidy N, Ruch JV. Experimental induction of odontoblast differentiation and stimulation during reparative processes. Cells Materials 1993;3:201–217.

      214. Tziafas D. Basic mechanisms of cytodifferentiation and dentinogenesis during dental pulp repair. Int J Dev Biol 1995;39:281–290.

      215. Tziafas D, Papadimitriou S. Role of exogenous TGF-β in induction of reparative dentinogenesis in vivo. Eur J Oral Sci 1998;106:192–196.

      216. Yoshiba K, Yoshiba N, Nakamura H, Iwaku M, Ozawa H. Immunolocalization of fibronectin during reparative dentinogenesis in human teeth after pulp capping with calcium hydroxide. J Dent Res 1996;75:1590–1597.

      217. Rutherford RB, Spångberg L, Tucker M, Rueger D, Charette M. The time-course of the induction of reparative dentine formation in monkeys by recombinant human osteogenic protein-1. Arch Oral Biol 1994;39:833–838.

      218. Nakashima M. Induction of dentine in amputated pulp of dogs by recombinant human bone morphogenetic proteins-2 and -4 with collagen matrix. Arch Oral Biol 1994;39: 1085–1089.

      219. Rutherford B, Spångberg L, Tucker M, Charette M. Transdentinal stimulation of reparative dentine formation by osteogenic protein-1 in monkeys. Arch Oral Biol 1995;40:681–683.

      220. Sasaki T, Kawamata-Kido H. Providing an environment for reparative dentine induction in amputated rat molar pulp by high molecular–weight hyaluronic acid. Arch Oral Biol 1995;40:209–219.

      221. Imai Y, Akimoto T. A new method of treatment for dentin hypersensitivity by precipitation of calcium phosphate in situ. Dent Mater J 1990;9:167–172.

      222. Pashley DH. Dentin permeability, dentin sensitivity, and treatment through tubule occlusion. J Endod 1986;12:465–474.

      223. Ishikawa K, Suge T, Yoshiyama M, Kawasaki A, Asaoka K, Ebisu S. Occlusion of dentinal tubules with calcium phosphate using acidic calcium phosphate solution followed by neutralization. J Dent Res 1994;73:1197–1204.

      224. Bjorndal L, Thylstrup A. A structural analysis of approximal enamel caries lesions and subjacent dentin reactions. Scand J Dent Res 1995;103:25–31.

      225. Love RM, Jenkinson HF. Invasion of dentinal tubules by oral bacteria. Crit Rev Oral Biol Med 2002;13:171–183.

      226. Veis A. Phosphoproteins of dentin and bone: Do they have a role in matrix mineralization? In: Butler WT (ed). The Chemistry and Biology of Mineralized Tissues. Birmingham, AL: EBSCO Media, 1985:170–176.

       Enamel

      During the early stage of tooth formation, the enamel organ consists of the outer enamel epithelium (OEE), the cells of the stellate reticulum (SR), the stratum intermedium (SI), and the inner enamel epithelium (IEE) (see Fig 1-6). The cells of the outer enamel epithelium are generally cuboidal. They attach by hemidesmosomes to a basal lamina separating them from the adjacent dental sac, a connective tissue of ectomesenchymal origin. Cytoplasmic organelles in the OEE include a moderate number of mitochondria, a small number of cisterns of rough endoplasmic reticulum (RER) and smooth endoplasmic reticulum, and a poorly developed Golgi complex. The presence of coated vesicles in the peripheral cytoplasm and along the plasma membrane facing the basal lamina suggests that the OEE is involved in specific endocytosis of extracelluar substances.

      Soon after the onset of enamel formation, the OEE becomes convoluted by indentations of highly vascularized connective tissue. This structural change becomes pronounced during enamel maturation, when the OEE, the SR, and the SI form the papillary layer to increase the surface area between the enamel organ and the adjacent blood supply. This change is pronounced in the continuously developing incisor of the rat, the most thoroughly investigated model of tooth development.

      The cells of the