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Tissue engineering of bone: the reconstructive surgeon's point of view.骨组织工程:重建外科医生的观点。
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Angiogenic and cell survival functions of vascular endothelial growth factor (VEGF).血管内皮生长因子(VEGF)的血管生成及细胞存活功能
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Differentiation of osteoblasts in three-dimensional culture in processed cancellous bone matrix: quantitative analysis of gene expression based on real-time reverse transcription-polymerase chain reaction.在处理过的松质骨基质中三维培养的成骨细胞分化:基于实时逆转录-聚合酶链反应的基因表达定量分析。
Tissue Eng. 2005 May-Jun;11(5-6):855-64. doi: 10.1089/ten.2005.11.855.
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Engineering bone: challenges and obstacles.工程化骨组织:挑战与障碍
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Biomaterials. 2005 Jun;26(16):3173-85. doi: 10.1016/j.biomaterials.2004.08.020.
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Modulation of in vitro angiogenesis in a three-dimensional spheroidal coculture model for bone tissue engineering.用于骨组织工程的三维球体共培养模型中体外血管生成的调控
Tissue Eng. 2004 Sep-Oct;10(9-10):1536-47. doi: 10.1089/ten.2004.10.1536.
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Localized ridge augmentation with a block allograft followed by secondary implant placement: a case report.采用块状同种异体骨进行局部牙槽嵴增量并二期植入种植体:病例报告
Int J Periodontics Restorative Dent. 2004 Feb;24(1):11-7.
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Stimulation of in vivo angiogenesis by cytokine-loaded hyaluronic acid hydrogel implants.细胞因子负载透明质酸水凝胶植入物对体内血管生成的刺激作用。
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Long-term stability of bone tissues induced by an osteoinductive biomaterial, recombinant human bone morphogenetic protein-2 and a biodegradable carrier.一种骨诱导生物材料、重组人骨形态发生蛋白-2和可生物降解载体诱导的骨组织长期稳定性。
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Tissue engineering skin flaps: which vascular carrier, arteriovenous shunt loop or arteriovenous bundle, has more potential for angiogenesis and tissue generation?组织工程皮瓣:哪种血管载体,动静脉分流环还是动静脉束,在血管生成和组织形成方面具有更大的潜力?
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在临界大小颅骨缺损大鼠模型中对接种同基因成骨细胞的处理后牛松质骨基质进行评估。

Evaluation of processed bovine cancellous bone matrix seeded with syngenic osteoblasts in a critical size calvarial defect rat model.

作者信息

Kneser U, Stangenberg L, Ohnolz J, Buettner O, Stern-Straeter J, Möbest D, Horch R E, Stark G B, Schaefer D J

机构信息

Department of Plastic and Hand Surgery, University of Erlangen Medical Center, Erlangen, Germany.

出版信息

J Cell Mol Med. 2006 Jul-Sep;10(3):695-707. doi: 10.1111/j.1582-4934.2006.tb00429.x.

DOI:10.1111/j.1582-4934.2006.tb00429.x
PMID:16989729
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3933151/
Abstract

INTRODUCTION

Biologic bone substitutes may offer alternatives to bone grafting procedures. The aim of this study was to evaluate a preformed bone substitute based on processed bovine cancellous bone (PBCB) with or without osteogenic cells in a critical size calvarial defect rat model.

METHODS

Discs of PBCB (Tutobone) were seeded with second passage fibrin gel-immobilized syngenic osteoblasts (group A, n = 40). Cell-free matrices (group B, n = 28) and untreated defects (group C; n=28) served as controls. Specimens were explanted between day 0 and 4 months after implantation and were subjected to histological and morphometric evaluation.

RESULTS

At 1 month, bone formation was limited to small peripheral areas. At 2 and 4 months, significant bone formation, matrix resorption as well as integration of the implants was evident in groups A and B. In group C no significant regeneration of the defects was observed. Morphometric analysis did not disclose differences in bone formation in matrices from groups A and B. Carboxyfluorescine-Diacetate-Succinimidylester (CFDA) labeling demonstrated low survival rates of transplanted cells.

DISCUSSION

Osteoblasts seeded into PBCB matrix display a differentiated phenotype following a 14 days cell culture period. Lack of initial vascularization may explain the absence of added osteogenicity in constructs from group A in comparison to group B. PBCB is well integrated and represents even without osteogenic cells a promising biomaterial for reconstruction of critical size calvarial bone defects.

摘要

引言

生物骨替代物可能为骨移植手术提供替代方案。本研究的目的是在大鼠颅骨临界尺寸缺损模型中评估一种基于处理过的牛松质骨(PBCB)的预制骨替代物,该替代物添加或未添加成骨细胞。

方法

将第二代纤维蛋白凝胶固定的同基因成骨细胞接种到PBCB(Tutobone)圆盘上(A组,n = 40)。无细胞基质(B组,n = 28)和未处理的缺损(C组,n = 28)作为对照。在植入后0至4个月之间取出标本,进行组织学和形态计量学评估。

结果

1个月时,骨形成仅限于小的周边区域。在2个月和4个月时,A组和B组均有明显的骨形成、基质吸收以及植入物整合。C组未观察到缺损的明显再生。形态计量学分析未发现A组和B组基质中骨形成的差异。羧基荧光素二乙酸琥珀酰亚胺酯(CFDA)标记显示移植细胞的存活率较低。

讨论

接种到PBCB基质中的成骨细胞在14天的细胞培养期后表现出分化的表型。与B组相比,A组构建体中缺乏初始血管化可能解释了其额外成骨作用不足的原因。PBCB整合良好,即使没有成骨细胞,也是用于重建颅骨临界尺寸骨缺损的一种有前景的生物材料。