[体外培养小鼠胎儿顶骨初始钙化的超微结构研究]。

T Oshiro
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引用次数: 0

摘要

从妊娠后期小鼠胎骨(去骨膜)中提取的顶骨碎片(1.5 mm平方)在含有10%胎牛血清的α - mem中培养10天,随后利用电镜和组织化学方法检查初始钙化部位。在初始钙化部位,观察到所谓的“基质囊泡”(宽度100 nm),来自诱导基质形成的成骨细胞,以及来自退化或死亡细胞的更大的囊泡结构(宽度100-600 nm)。此外,死亡的成骨细胞样细胞吞噬骨晶体参与了骨结节的形成。在退化或破坏细胞与功能细胞之间的边界区域,经常观察到多层结构(主要由磷脂组成)。同时得出结论,在某些情况下,上述细胞表面可能存在钙盐的部分沉积。通过选择性脱钙,确定骨小梁是由各自的骨结节和降解的胶原原纤维融合形成的,胶原原纤维填充间隙。从以上结果可以看出,来自功能成骨细胞的基质囊泡和来自同时吞噬针状体和胶原原纤维的退化或死亡细胞的囊泡结构都参与了体外膜性骨的初始钙化过程。
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[Ultrastructural studies of initial calcification of mouse fetal parietal bone in vitro].

The parietal bone fragment (1.5 mm square) extracted from murine fetal calvaria (periosteum was removed) in the latter stage of gestation was cultured in alpha-MEM containing 10% fetal bovine serum over 10-day period, and the initial calcification site was subsequently examined utilizing both electron microscopy and histochemical methods. At the initial calcification site, the so-called "matrix vesicle" (width 100 nm), derived from osteoblasts which induce matrix formation, and the larger vesicular structures (width 100-600 nm) which originated from degenerated or dead cells were observed. Additionally dead osteoblast-like cells phagocytosing bone crystals participated in bone nodul formation. In the border region between the degenerated or disrupted cells and the functioning cells, multilamellar structures (mainly composed of phospholipids) were frequently observed. Concurrently it was concluded that there is a possibility of partial deposition of calcium salts on the surface of the above mentioned cells under some circumstances. Through selective decalcification, it was determined that bone trabecule was formed by fusion of respective bone noduli and degraded collagen fibrils which filled the intervening spaces. From the above results, it was evident that both the matrix vesicles derived from functioning osteoblast, and the vesicular structures derived from the degenerated or dead cells concurrently phagocytosing spicules and collagen fibrils were involved in the initial calcification process of the membranous bone in vitro.

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