McKee M D, Zalzal S, Nanci A
Department of Stomatology, Faculty of Dentistry, Université de Montréal, Quebec, Canada.
Anat Rec. 1996 Jun;245(2):293-312. doi: 10.1002/(SICI)1097-0185(199606)245:2<293::AID-AR13>3.0.CO;2-K.
Noncollagenous proteins (NCPs) are considered to have multiple functions related to the formation, turnover, and repair of the collagen-based mineralized tissues. Collectively, they comprise a class of generally acidic, mineral-binding proteins showing extensive posttranslational modifications, including glycosylation, phosphorylation, and sulfation. METHODS. We have used colloidal-gold immunocytochemistry and lectin-gold cytochemistry, together with transmission electron microscopy, to examine the organic matrix composition of tooth cementum and the subjacent mantle dentin in rodent molar teeth. Molars were processed for immunocytochemistry using antibodies against osteopontin (OPN), osteocalcin (OC), bone sialoprotein (BSP), bone acidic glycoprotein-75 (BAG-75), albumin (ALB), and alpha 2HS-glycoprotein (alpha 2HS-GP), or for glycoconjugate cytochemistry using lectin-gold complexes.
Ultrastructurally, at the advancing root edge in developing molars, OPN and BSP initially were associated with small calcification foci in the mantle dentin. With progressing mineralization, OC and alpha 2HS-GP appeared diffusely distributed throughout the calcified mantle dentin, and diminished as a gradient toward the circumpulpal dentin. Immediately following disruption of Hertwig's epithelial root sheath, cementum deposition commenced at the root surface occasionally with the appearance of a cement line rich in OPN. Cementum matrix proper contained abundant OPN, BSP, OC, and alpha 2HS-GP, but no or little BAG-75 or ALB. Protein immunolabeling, as well as lectin labeling for beta-D-galactose and N-acetyl-neuraminic acid and/or N-glycolyl-neuraminic acid, both being prominent sugars of certain NCPs, was primarily concentrated between, and at the surface of, collagen fibrils in acellular extrinsic fiber cementum. OPN, BSP, OC, and alpha 2HS-GP were also prominent components of cellular cementum and of Sharpey's fibers. In cellular cementum, laminae limitantes sometimes present delimiting cementocyte lacunae and cell process-containing canaliculi were also rich in OPN. Along the root surface, occasional cementoblasts exhibited intracellular labeling for OPN over the Golgi apparatus and secretory granules.
We have identified OPN, BSP, OC, and alpha 2HS-GP as being prominent organic constituents of both mantle dentin and acellular and cellular cementum, and, have elucidated the details of their distribution at the ultrastructural level. The temporal appearance and spatial distribution of these organic moieties in the teeth root are similar to those seen during bone formation and are consistent with proposals that certain NCPs may be involved in regulating calcification and/or participating in cell-matrix and matrix-matrix/mineral adhesion events.
非胶原蛋白(NCPs)被认为具有多种与基于胶原蛋白的矿化组织的形成、更新和修复相关的功能。它们共同构成了一类通常呈酸性的矿质结合蛋白,显示出广泛的翻译后修饰,包括糖基化、磷酸化和硫酸化。方法:我们使用胶体金免疫细胞化学和凝集素-金细胞化学,结合透射电子显微镜,来检查啮齿动物磨牙牙骨质和相邻罩牙本质的有机基质组成。使用针对骨桥蛋白(OPN)、骨钙素(OC)、骨唾液蛋白(BSP)、骨酸性糖蛋白-75(BAG-75)、白蛋白(ALB)和α2HS-糖蛋白(α2HS-GP)的抗体对磨牙进行免疫细胞化学处理,或使用凝集素-金复合物进行糖缀合物细胞化学处理。
在超微结构上,在发育中的磨牙的牙根前缘,OPN和BSP最初与罩牙本质中的小钙化灶相关。随着矿化进展,OC和α2HS-GP呈弥漫性分布于整个钙化的罩牙本质中,并向牙髓周围牙本质呈梯度减少。赫特维希上皮根鞘破坏后立即开始,牙骨质在牙根表面沉积,偶尔会出现富含OPN的牙骨质线。牙骨质基质本身含有丰富的OPN、BSP、OC和α2HS-GP,但没有或几乎没有BAG-75或ALB。蛋白质免疫标记以及针对β-D-半乳糖和N-乙酰神经氨酸和/或N-糖基神经氨酸的凝集素标记,这两种都是某些NCPs的主要糖类标记,主要集中在无细胞外源性纤维牙骨质中胶原纤维之间及其表面。OPN、BSP、OC和α2HS-GP也是细胞性牙骨质和沙比纤维的主要成分。在细胞性牙骨质中,有时存在的限制牙骨质细胞陷窝和含有细胞突起的小管的界膜也富含OPN。沿着牙根表面,偶尔的成牙骨质细胞在高尔基体和分泌颗粒上显示出OPN的细胞内标记。
我们已确定OPN、BSP、OC和α2HS-GP是罩牙本质以及无细胞和细胞性牙骨质的主要有机成分,并在超微结构水平上阐明了它们分布的细节。这些有机成分在牙根中的出现时间和空间分布与骨形成过程中所见相似,并且与某些NCPs可能参与调节钙化和/或参与细胞-基质和基质-基质/矿物质粘附事件的提议一致。