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鸡生长板软骨细胞原代培养物在含抗坏血酸培养基中诱导矿物质沉积。基质小泡与胶原蛋白之间关联的证据。

Induction of mineral deposition by primary cultures of chicken growth plate chondrocytes in ascorbate-containing media. Evidence of an association between matrix vesicles and collagen.

作者信息

Wu L N, Sauer G R, Genge B R, Wuthier R E

机构信息

Department of Chemistry, University of South Carolina, Columbia 29208.

出版信息

J Biol Chem. 1989 Dec 15;264(35):21346-55.

PMID:2592380
Abstract

A serum-free primary culture system for chicken growth plate chondrocytes has been developed which consistently undergoes mineral deposition. Upon attainment of confluency, the chondrocytes develop locally into multilayer cellular nodules leading to matrix calcification. Mineralization first occurs in matrix vesicles (MV) that are abundant in the extraterritorial matrix between the hypertrophic cells. Studies with 45Ca reveal that significant accumulation of Ca2+ occurs as early as day 12, continuing progressively throughout the culture period. By day 24, the nodules become densely calcified. Fourier transform infrared spectroscopy reveals the mineral to be similar to apatite, with features essentially identical to those of mineral formed by MV in vitro. The presence of ascorbate is critical to the culture system; in its absence, calcification is rarely observed. Ascorbate stimulates MV formation and synthesis of cellular protein, alkaline phosphatase, and especially types II and X collagens. In addition, there is strong evidence that the types II and X collagens are associated with MV. 1) Electron microscopy reveals MV embedded in a type II collagenous network; 2) Western blots of sodium dodecyl sulfate-polyacrylamide gel electrophoresis of MV using monospecific antibodies to types X and II collagen indicate that both collagens are present in specific MV fractions; 3) sucrose gradient purification of MV does not remove associated collagens; 4) graded salt extraction selectively releases type II collagen from MV; and 5) incubation of radiolabeled types II and X collagens with MV leads to their cosedimentation upon subsequent centrifugation. Taken together, the data suggest that coordinated synthesis of the collagens, alkaline phosphatase, MV formation, and Ca2+ accumulation by the cultures combine to induce mineral deposition in the multilayer nodules.

摘要

已开发出一种用于鸡生长板软骨细胞的无血清原代培养系统,该系统持续发生矿物质沉积。达到汇合状态时,软骨细胞局部发育成多层细胞结节,导致基质钙化。矿化首先发生在肥大细胞之间域外基质中丰富的基质小泡(MV)中。用45Ca进行的研究表明,早在第12天就发生了Ca2+的显著积累,并在整个培养期持续逐渐增加。到第24天,结节变得密集钙化。傅里叶变换红外光谱显示该矿物质类似于磷灰石,其特征与体外由MV形成的矿物质基本相同。抗坏血酸的存在对培养系统至关重要;没有抗坏血酸时,很少观察到钙化。抗坏血酸刺激MV形成以及细胞蛋白、碱性磷酸酶,尤其是II型和X型胶原蛋白的合成。此外,有强有力的证据表明II型和X型胶原蛋白与MV相关。1)电子显微镜显示MV嵌入II型胶原网络中;2)使用针对X型和II型胶原蛋白的单特异性抗体对MV进行十二烷基硫酸钠-聚丙烯酰胺凝胶电泳的蛋白质印迹表明,两种胶原蛋白都存在于特定的MV组分中;3)MV的蔗糖梯度纯化并未去除相关的胶原蛋白;4)分级盐提取选择性地从MV中释放II型胶原蛋白;5)用放射性标记的II型和X型胶原蛋白与MV一起孵育,随后离心会导致它们共同沉降。综上所述,数据表明培养物中胶原蛋白、碱性磷酸酶、MV形成和Ca2+积累的协同合成共同诱导多层结节中的矿物质沉积。

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