Sampath T K, Reddi A H
Proc Natl Acad Sci U S A. 1981 Dec;78(12):7599-603. doi: 10.1073/pnas.78.12.7599.
Subcutaneous implantation of demineralized diaphyseal bone matrix in allogeneic rats results in the local induction of endochondral bone differentiation. We have explored the potential of three dissociative extractants, 4 M guanidine hydrochloride (Gdn . HCl), 8 M urea/1 M NaCl, and 1% NaDodSO4 at pH 7.4, containing protease inhibitors to solubilize putative inductive molecules in the bone matrix. Extraction of bone matrix with any one of these extracts resulted in the loss of the bone inductive property. The solubilized extracts were then reconstituted with the residue by dialysis against water. The various reconstituted matrices were bioassayed for bone inductive potential by quantitation of alkaline phosphatase activity and 45Ca incorporation on day 12 after implantation. There was complete recovery of biological activity after reconstitution of the residues with each of the three extracts. Polyacrylamide gel electrophoresis of the extracts revealed similar protein profiles. Gel filtration of the 4 M Gdn. HCl extract on Sepharose CL-4B showed a heterogeneous broad peak. When fractions of that peak containing proteins less than 50,000 daltons were reconstituted with inactive 4 M Gdn . HCl-treated bone matrix and then implanted, new bone was induced. These observations demonstrate the dissociative extraction and successful biological reconstitution of bone inductive macromolecules in demineralized bone matrix.
在同种异体大鼠皮下植入脱矿骨干骨基质可导致软骨内骨分化的局部诱导。我们探索了三种解离萃取剂的潜力,即含有蛋白酶抑制剂的4M盐酸胍(Gdn.HCl)、8M尿素/1M氯化钠和pH7.4的1%十二烷基硫酸钠,以溶解骨基质中假定的诱导分子。用这些萃取剂中的任何一种萃取骨基质都会导致骨诱导特性丧失。然后通过对水进行透析,将溶解的萃取物与残渣重新组合。在植入后第12天,通过定量碱性磷酸酶活性和45Ca掺入量,对各种重新组合的基质进行骨诱导潜力的生物测定。用三种萃取剂中的每一种将残渣重新组合后,生物活性完全恢复。萃取物的聚丙烯酰胺凝胶电泳显示出相似的蛋白质谱。4M Gdn.HCl萃取物在琼脂糖CL-4B上进行凝胶过滤显示出一个异质性宽峰。当用无活性的4M Gdn.HCl处理的骨基质对该峰中分子量小于50,000道尔顿的蛋白质部分进行重组,然后植入时,可诱导出新骨。这些观察结果证明了脱矿骨基质中骨诱导大分子的解离萃取和成功的生物重组。