Expression of bone matrix proteins during de novo bone formation using a bovine collagen and platelet-rich plasma (prp) - an immunohistochemical analysis

被引:88
作者
Thorwarth, M
Rupprecht, S
Falk, S
Felszeghy, E
Wiltfang, J
Schlegel, KA
机构
[1] Univ Erlangen Nurnberg, Dept Maxillofacial Surg, D-91054 Erlangen, Germany
[2] Univ Erlangen Nurnberg, Dept Operat Dent & Periodontol, D-91054 Erlangen, Germany
[3] Semmelweis Ovostudomanyi Egyetem, Inst Forens Med, HU-1091 Budapest, Hungary
[4] Univ Schleswig Holstein, Dept Maxillofacial Surg, D-24105 Kiel, Germany
关键词
platelet-rich plasma; bovine collagen; bone regeneration; prospective study; bone substitutes; bone matrix proteins;
D O I
10.1016/j.biomaterials.2004.07.041
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
This animal study (domestic pig) examined the bone formation after filling defined defects with autogenous bone or a collagen lyophilisat in combination with Platelet-rich-plasma (PRP) by evaluating bone matrix proteins. Six groups, both materials with and without PRP in two concentrations (+1, +2) were compared to untreated bone by means of immunohistochemistry at 2, 4, 12 and 26 weeks. BMP-2 expression was increased at 2 weeks in the collagen +1 group and after 4 weeks in the collagen +1 and + 2 group. Collagen-I expression was increased at 2 weeks in all collagen groups. After 4 weeks raised levels were observed after adding the higher concentrated PRP to bone and the collagen material. Osteocalcin expression was enhanced at 2 weeks in all collagen groups and the autogenous bone + PRP1 group, after 4 weeks in the bone and collagen +2 groups. At 12 weeks higher values were observed after adding higher concentrated PRP to bone. Osteonectin and especially osteopontin were confirmed to be effective markers of early bone formation in all specimens. The described setting allows to combine established techniques (microradiography, light microscopy) with approaches to explore the underlying biology (immunohistochemistry) on the same specimen. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2575 / 2584
页数:10
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