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苯那明的递送增强了BMP-2诱导的脂肪来源干细胞的成骨分化及颅骨缺损中的骨形成。

Delivery of Phenamil Enhances BMP-2-Induced Osteogenic Differentiation of Adipose-Derived Stem Cells and Bone Formation in Calvarial Defects.

作者信息

Fan Jiabing, Im Choong Sung, Cui Zhong-Kai, Guo Mian, Bezouglaia Olga, Fartash Armita, Lee Ju-Yeon, Nguyen John, Wu Benjamin M, Aghaloo Tara, Lee Min

机构信息

1 Division of Advanced Prosthodontics, UCLA School of Dentistry , Los Angeles, California.

2 Department of Neurosurgery, the 2nd Affiliated Hospital of Harbin Medical University , Harbin, China .

出版信息

Tissue Eng Part A. 2015 Jul;21(13-14):2053-65. doi: 10.1089/ten.TEA.2014.0489. Epub 2015 May 20.

Abstract

Bone morphogenetic proteins (BMPs) have been widely used for bone repair in the craniofacial region. However, its high dose requirement in clinical applications revealed adverse effects and inefficient bone formation, along with high cost. Here, we report a novel osteoinductive strategy to effectively complement the osteogenic activity of BMP-2 using phenamil, a small molecule that can induce osteogenic differentiation via stimulation of BMP signaling. Treatment of adipose-derived stem cells (ASCs) with BMP-2 in combination with phenamil significantly promoted the in vitro osteogenic differentiation of ASCs. The efficacy of the combination strategy of phenamil+BMP-2 was further confirmed in a mouse calvarial defect model using scaffolds consisting of poly(lactic-co-glycolic acid) and apatite layer on their surfaces designed to slowly release phenamil and BMP-2. Six weeks after implantation, the scaffolds treated with phenamil+BMP-2 significantly promoted mouse calvarial regeneration as demonstrated by micro-computerized tomography and histology, compared with the groups treated with phenamil or BMP-2 alone. Moreover, the combination treatment reduced the BMP-2 dose without compromising calvarial healing efficacy. These results suggest promising complementary therapeutic strategies for bone repair in more efficient and cost-effective manners.

摘要

骨形态发生蛋白(BMPs)已被广泛应用于颅面部骨修复。然而,其在临床应用中的高剂量需求显示出不良反应、骨形成效率低下以及成本高昂。在此,我们报告一种新型的骨诱导策略,使用苯那明(一种可通过刺激BMP信号诱导成骨分化的小分子)有效补充BMP-2的成骨活性。用BMP-2联合苯那明处理脂肪来源干细胞(ASCs)可显著促进ASCs的体外成骨分化。在小鼠颅骨缺损模型中,使用表面设计为可缓慢释放苯那明和BMP-2的聚乳酸-乙醇酸共聚物和磷灰石层组成的支架,进一步证实了苯那明+BMP-2联合策略的有效性。植入六周后,与单独使用苯那明或BMP-2处理的组相比,经苯那明+BMP-2处理的支架通过微计算机断层扫描和组织学显示显著促进了小鼠颅骨再生。此外,联合治疗降低了BMP-2的剂量,同时不影响颅骨愈合效果。这些结果表明,有望以更高效和经济有效的方式为骨修复提供互补性治疗策略。

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