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从血清到矿化相。成牙本质细胞在钙转运和矿化形成中的作用。

From serum to the mineral phase. The role of the odontoblast in calcium transport and mineral formation.

作者信息

Linde A, Lundgren T

机构信息

Department of Oral Biochemistry, Faculty of Odontology, Göteborg University, Sweden.

出版信息

Int J Dev Biol. 1995 Feb;39(1):213-22.

PMID:7626409
Abstract

Dentin may be considered as a calcified connective tissue and is in its composition as well as in its mode of formation closely related to bone. Dentin is formed by two simultaneous processes in which the odontoblasts are instrumental: the formation of the proteinaceous dentin matrix, and mineral crystal formation in this matrix. As part of this, the odontoblasts actively transport Ca2+ ions towards the site of mineral formation. The cells maintain a delicate intracellular Ca2+ ion balance by the concerted action of transmembraneous transport mechanisms, including Ca-ATPase, Na+/Ca2+ exchangers and calcium channels of the L-type, and possibly intracellular Ca(2+)-binding proteins. The net effect of this is a maintenance of a cytoplasmic sub-micromolar Ca2+ activity and an extracellular accumulation of Ca2+ ions at the mineralization front. In addition to the major matrix constituent, collagen, non-collagenous macromolecules, such as dentin phosphoprotein (phosphophoryn), dentin sialoprotein, and proteoglycan, are synthesized by the odontoblasts and deposited in the matrix. Such polyanionic macromolecules are presumably responsible for the extracellular induction of hydroxyapatite crystals, but may also function to inhibit mineral growth and to regulate crystal size. Accordingly, it can be concluded that dentinogenesis comprises an interplay between several factors in the tissue, cellular as well as extracellular.

摘要

牙本质可被视为一种钙化的结缔组织,其组成和形成方式与骨密切相关。牙本质由成牙本质细胞起作用的两个同时进行的过程形成:蛋白质性牙本质基质的形成以及该基质中矿物质晶体的形成。在此过程中,成牙本质细胞将Ca2+离子主动转运至矿物质形成部位。细胞通过跨膜转运机制(包括Ca-ATP酶、Na+/Ca2+交换体和L型钙通道,可能还有细胞内Ca(2+)结合蛋白)的协同作用维持细胞内Ca2+离子的微妙平衡。其最终结果是维持细胞质亚微摩尔Ca2+活性以及在矿化前沿细胞外积累Ca2+离子。除了主要的基质成分胶原蛋白外,成牙本质细胞还合成非胶原蛋白大分子,如牙本质磷蛋白(磷酸磷蛋白)、牙本质涎蛋白和蛋白聚糖,并将其沉积在基质中。这种多阴离子大分子可能负责细胞外诱导羟基磷灰石晶体,但也可能起到抑制矿物质生长和调节晶体大小的作用。因此,可以得出结论,牙本质形成包括组织中细胞和细胞外多种因素之间的相互作用。

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