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抗牙本质磷蛋白单克隆抗体的研制:一种研究成牙本质细胞活性的工具。

Development of a monoclonal antibody against dentin phosphophoryn: a tool to study odontoblastic activity.

作者信息

Laboux O, Menanteau J, Pelhate S, Aubry J, Blottiere H M, Pouezat D, Jean A, Pouezat J A

机构信息

Laboratoire de Recherche sur les Tissus Calcifiés et les Biomatériaux, UFR d'Odontologie, Nantes, France.

出版信息

Hybridoma. 1994 Apr;13(2):143-6. doi: 10.1089/hyb.1994.13.143.

Abstract

The role played by phosphophoryn, one of the major noncollagenous proteins of dentin extracellular matrix, in the mineralization process has not been fully characterized. The purpose of our work was to produce monoclonal antibodies (MAbs) against dentin phosphophoryn and to test their reactivity with primary culture of odontoblasts. Dentin phosphophoryn (DPP) was extracted after the mechanical dissociation of teeth and dialyzed against guanidine and EDTA solutions followed by CaC1(2) precipitation. These extracts were characterized by SDS-PAGE and staining with Coomassie blue and Stains-All. After immunization of mice with these extracts, we produced MAb 7G4, which reacted with dentin phosphophoryn as revealed by Western blot. MAb 7G4 reactivity was tested against a primary culture of pig odontoblasts, revealing filaments specifically stained by the anti-DPP antibody. This antibody will be of great interest to study the mineralization process and dental pulp reaction after capping with various calcium phosphate materials.

摘要

牙本质细胞外基质的主要非胶原蛋白之一——磷蛋白在矿化过程中所起的作用尚未完全明确。我们研究的目的是制备抗牙本质磷蛋白的单克隆抗体(MAb),并检测其与成牙本质细胞原代培养物的反应性。牙齿经机械解离后提取牙本质磷蛋白(DPP),并先后用胍溶液和EDTA溶液进行透析,然后用CaC1₂沉淀。这些提取物通过SDS-PAGE以及考马斯亮蓝和全染染色进行表征。用这些提取物免疫小鼠后,我们制备了单克隆抗体7G4,蛋白质印迹显示该抗体与牙本质磷蛋白发生反应。针对猪成牙本质细胞原代培养物检测了单克隆抗体7G4的反应性,结果显示有细丝被抗DPP抗体特异性染色。该抗体对于研究用各种磷酸钙材料盖髓后的矿化过程和牙髓反应将具有重要意义。

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