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骨骺生长板矿物质形成初期的电子显微镜微探针分析

Electron-microscopic microprobe analysis on the initial stages of mineral formation in the epiphyseal growth plate.

作者信息

Barckhaus R H, Krefting E R, Althoff J, Quint P, Höhling H J

出版信息

Cell Tissue Res. 1981;217(3):661-6. doi: 10.1007/BF00219372.

DOI:10.1007/BF00219372
PMID:7249054
Abstract

Dry thin sections (300-500 nm thick) of shock-frozen, freeze-dried and embedded epiphyseal growth plates from the proximal tibia of guinea pigs were cut longitudinally from the plate. Dark round bodies (phi less than 0.5 micron) were observed using the scanning transmission mode of the electron microscope initially directly in the vicinity of the chondrocytes. They gradually spread out in the direction of the metaphysis to the center of the longitudinal septum and represent most probably the matrix vesicles. By use of a microscan of 0.25 X 0.25 micron the element-concentrations of these bodies were measured. The measurements started on those bodies that could be clearly recognized and were extended to a length of 30-40 micron in the metaphyseal direction. To obtain approximate quantitative results the registered CaK alpha and PK alpha x-ray counts were directly compared with counts of fully mineralized regions, the Ca and P contents of which are known. Ca as well as p could be detected in the first visible vesicle-like structures (Ca approximately 0.2%, P approximately 0.4%) and increased steeply in the metaphyseal direction, amounting to approximately 6% Ca and 3% P. These results may lead to the conclusion that Pi becomes split from phosphate esters and transformed into the matrix vesicles already in a very early stage of enrichment. Incorporation of Ca may be coupled with this process.

摘要

将豚鼠胫骨近端经冲击冷冻、冻干并包埋的骨骺生长板制成干燥薄片(300 - 500纳米厚),从生长板纵向切片。最初在软骨细胞附近直接使用电子显微镜的扫描透射模式观察到暗圆形物体(直径小于0.5微米)。它们逐渐向干骺端方向扩散至纵向隔膜中心,很可能代表基质小泡。通过使用0.25×0.25微米的微扫描测量这些物体的元素浓度。测量从那些能够清晰识别的物体开始,并在干骺端方向延伸至30 - 40微米的长度。为了获得近似定量结果,将记录的钙Kα和磷Kα x射线计数直接与完全矿化区域的计数进行比较,已知其钙和磷含量。在最初可见的囊泡状结构中可检测到钙和磷(钙约0.2%,磷约0.4%),并在干骺端方向急剧增加,钙含量约为6%,磷含量约为3%。这些结果可能得出结论,即磷酸根离子在富集的非常早期阶段就从磷酸酯中分离出来并转化为基质小泡。钙的掺入可能与这个过程相关。

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引用本文的文献

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Calcif Tissue Int. 1994 Apr;54(4):296-303. doi: 10.1007/BF00295954.
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本文引用的文献

1
Mechanisms of calcification: role of collagen, polyphosphates, and phosphatase.钙化机制:胶原蛋白、多聚磷酸盐和磷酸酶的作用。
Am J Physiol. 1961 Jun;200:1296-300. doi: 10.1152/ajplegacy.1961.200.6.1296.
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Electron microscopic studies of induced cartilage development and calcification.诱导性软骨发育与钙化的电子显微镜研究。
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Isolation and characterization of calcifying matrix vesicles from epiphyseal cartilage.从骨骺软骨中分离和鉴定钙化基质小泡。
Proc Natl Acad Sci U S A. 1970 Nov;67(3):1513-20. doi: 10.1073/pnas.67.3.1513.
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A low-viscosity epoxy resin embedding medium for electron microscopy.一种用于电子显微镜的低粘度环氧树脂包埋介质。
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Chemical modifications in osteones during calcification.钙化过程中骨单位的化学修饰
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Fine structure of early cartilage calcification.早期软骨钙化的精细结构
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7
Loss of proteinpolysaccharides at sites where bone mineralization is initiated.在骨矿化起始部位蛋白多糖的缺失。
J Histochem Cytochem. 1972 Apr;20(4):279-92. doi: 10.1177/20.4.279.
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The sequence of calcium and phosphorus accumulation by matrix vesicles.
Calcif Tissue Res. 1977 May;22 Suppl:490-3. doi: 10.1007/BF02064139.
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Biosynthesis of matrix vesicles in epiphyseal cartilage. I. In vivo incorporation of 32P orthophosphate into phospholipids of chondroxyte, membrane, and matrix vesicle fractions.
Calcif Tissue Res. 1977 Jun 28;23(2):135-9. doi: 10.1007/BF02012778.
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Electrolytes of isolated epiphyseal chondrocytes, matrix vesicles, and extracellular fluid.分离的骨骺软骨细胞、基质小泡和细胞外液的电解质。
Calcif Tissue Res. 1977 Jun 28;23(2):125-33. doi: 10.1007/BF02012777.