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Peptide drugs accelerate BMP-2-induced calvarial bone regeneration and stimulate osteoblast differentiation through mTORC1 signaling.肽类药物通过mTORC1信号通路加速BMP - 2诱导的颅骨再生并刺激成骨细胞分化。
Bioessays. 2016 Aug;38(8):717-25. doi: 10.1002/bies.201600104. Epub 2016 Jun 27.
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Bone regeneration in calvarial defects in a rat model by implantation of human bone marrow-derived mesenchymal stromal cell spheroids.通过植入人骨髓间充质基质细胞球体实现大鼠颅骨缺损的骨再生
J Mater Sci Mater Med. 2015 Nov;26(11):254. doi: 10.1007/s10856-015-5591-3. Epub 2015 Oct 8.
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Epigenetic Control of Skeletal Development by the Histone Methyltransferase Ezh2.组蛋白甲基转移酶Ezh2对骨骼发育的表观遗传调控
J Biol Chem. 2015 Nov 13;290(46):27604-17. doi: 10.1074/jbc.M115.672345. Epub 2015 Sep 30.
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Establishing criteria for human mesenchymal stem cell potency.建立人间充质干细胞效力标准。
Stem Cells. 2015 Jun;33(6):1878-91. doi: 10.1002/stem.1982.
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Induction of fully stabilized cortical bone defects to study intramembranous bone regeneration.诱导完全稳定的皮质骨缺损以研究膜内骨再生。
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Enhanced healing of rat calvarial defects with MSCs loaded on BMP-2 releasing chitosan/alginate/hydroxyapatite scaffolds.负载于释放骨形态发生蛋白-2的壳聚糖/海藻酸盐/羟基磷灰石支架上的间充质干细胞促进大鼠颅骨缺损的愈合
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Runx2 is required for early stages of endochondral bone formation but delays final stages of bone repair in Axin2-deficient mice.Runx2对于软骨内骨形成的早期阶段是必需的,但在Axin2基因缺陷小鼠中会延迟骨修复的最后阶段。
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Histological remodelling of demineralised bone matrix allograft in posterolateral fusion of the spine--an ex vivo study.脱矿骨基质同种异体移植物在脊柱后外侧融合中的组织学重塑——一项体外研究
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The influence of collagen and hyaluronan matrices on the delivery and bioactivity of bone morphogenetic protein-2 and ectopic bone formation.胶原和透明质酸基质对骨形态发生蛋白-2 的传递和生物活性及异位骨形成的影响。
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一种用于研究小鼠模型颅骨骨缺损愈合的多功能方案。

A Versatile Protocol for Studying Calvarial Bone Defect Healing in a Mouse Model.

机构信息

1 Department of Orthopedic Surgery, Mayo Clinic , Rochester, Minnesota.

2 Glycotherapeutics Group, Institute of Medical Biology , Agency for Science, Technology and Research (A*STAR), Singapore .

出版信息

Tissue Eng Part C Methods. 2017 Nov;23(11):686-693. doi: 10.1089/ten.TEC.2017.0205. Epub 2017 Jul 3.

DOI:10.1089/ten.TEC.2017.0205
PMID:28537529
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5689119/
Abstract

Animal models are vital tools for the preclinical development and testing of therapies aimed at providing solutions for several musculoskeletal disorders. For bone tissue engineering strategies addressing nonunion conditions, rodent models are particularly useful for studying bone healing in a controlled environment. The mouse calvarial defect model permits evaluation of drug, growth factor, or cell transplantation efficacy, together with offering the benefit of utilizing genetic models to study intramembranous bone formation within defect sites. In this study, we describe a detailed methodology for creating calvarial defects in mouse and present our results on bone morphogenetic protein-2-loaded fibrin scaffolds, thus advocating the utility of this functional orthotopic mouse model for the evaluation of therapeutic interventions (such as growth factors or cells) intended for successful bone regeneration therapies.

摘要

动物模型是针对几种肌肉骨骼疾病的治疗方法进行临床前开发和测试的重要工具。对于旨在解决骨不连的骨组织工程策略,啮齿动物模型特别有助于在受控环境中研究骨愈合。小鼠颅骨缺损模型允许评估药物、生长因子或细胞移植的疗效,同时还可以利用遗传模型来研究缺陷部位内的膜内骨形成。在这项研究中,我们描述了一种在小鼠中创建颅骨缺损的详细方法,并介绍了我们关于骨形态发生蛋白 2 负载纤维蛋白支架的结果,从而提倡使用这种功能性原位小鼠模型来评估旨在成功进行骨再生治疗的治疗干预(如生长因子或细胞)。