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脱矿骨基质在肌内植入物中的骨诱导作用:胶原合成的序列变化

Bone induction in intramuscular implants by demineralized bone matrix: sequential changes of collagen synthesis.

作者信息

Guterman I A, Boman T E, Wang G J, Balian G

机构信息

Department of Orthopaedics and Rehabilitation, University of Virginia School of Medicine, Charlottesville 22908.

出版信息

Coll Relat Res. 1988 Sep;8(5):419-31. doi: 10.1016/s0174-173x(88)80015-3.

Abstract

Implantation of rat demineralized bone matrix into intramuscular pouches has been shown to cause a complex cellular transition of mesenchymal-type cells into well developed mature bone. Demineralized bone matrix was surgically implanted into rat muscle pouches and removed at various intervals between 7 and 28 days. Histological sections of the implants revealed bone formation by endochondral ossification and appositional bone growth. Biochemical analysis of collagen synthesis demonstrated the following: (1) synthesis of type X collagen, a collagen produced by hypertrophic chondrocytes in the growth plate and in fracture callus. (2) Synthesis of a collagenase-sensitive 17k protein which seems to increase in the early stages of bone induction. Pulse chase analysis indicates that 17k is not a degradation product of another protein and appears to be synthesized without a large Mr precursor. The 17k component contains one or more collagenous domains that are partially resistant to proteolysis with pepsin. Our results confirm the appearance of a cartilage intermediate during demineralized bone matrix induced ossification and implicate the existence of proteins which may be useful markers in future studies on matrix mineralization and ossification.

摘要

已证明将大鼠脱矿骨基质植入肌袋会导致间充质型细胞发生复杂的细胞转变,进而形成发育良好的成熟骨。将脱矿骨基质通过手术植入大鼠肌袋,并在7至28天的不同时间间隔取出。植入物的组织学切片显示通过软骨内成骨和贴壁骨生长形成骨。胶原蛋白合成的生化分析表明:(1)X型胶原蛋白的合成,这种胶原蛋白由生长板和骨折痂中的肥大软骨细胞产生。(2)一种对胶原酶敏感的17k蛋白的合成,该蛋白似乎在骨诱导的早期阶段增加。脉冲追踪分析表明,17k不是另一种蛋白质的降解产物,并且似乎是在没有大分子量前体的情况下合成的。17k组分包含一个或多个对胃蛋白酶部分抗蛋白水解的胶原结构域。我们的结果证实了脱矿骨基质诱导骨化过程中软骨中间体的出现,并暗示了可能在未来基质矿化和骨化研究中作为有用标志物的蛋白质的存在。

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