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PCL-DA/PLLA 半互穿网络形状记忆聚合物支架的固有成骨活性。

Intrinsic osteoinductivity of PCL-DA/PLLA semi-IPN shape memory polymer scaffolds.

机构信息

Department of Biomedical Engineering, Rensselaer Polytechnic Institute (RPI), Troy, New York, USA.

Center for Biotechnology and Interdisciplinary Studies, Rensselaer Polytechnic Institute (RPI), Troy, New York, USA.

出版信息

J Biomed Mater Res A. 2021 Nov;109(11):2334-2345. doi: 10.1002/jbm.a.37216. Epub 2021 May 14.

Abstract

Engineering osteoinductive, self-fitting scaffolds offers a potential treatment modality to repair irregularly shaped craniomaxillofacial bone defects. Recently, we innovated on osteoinductive poly(ε-caprolactone)-diacrylate (PCL-DA) shape memory polymers (SMPs) to incorporate poly-L-lactic acid (PLLA) into the PCL-DA network, forming a semi-interpenetrating network (semi-IPN). Scaffolds formed from these PCL-DA/PLLA semi-IPNs display stiffnesses within the range of trabecular bone and accelerated degradation relative to scaffolds formed from slowly degrading PCL-DA SMPs. Herein, we demonstrate for the first time that PCL-DA/PLLA semi-IPN SMP scaffolds show increased intrinsic osteoinductivity relative to PCL-DA. We also confirm that application of a bioinspired polydopamine (PD) coating further improves the osteoinductive capacity of these PCL-DA/PLLA semi-IPN SMPs. In the absence of osteogenic supplements, protein level assessment of human mesenchymal stem cells (h-MSCs) cultured in PCL-DA/PLLA scaffolds revealed an increase in expression of osteogenic markers osterix, bone morphogenetic protein-4 (BMP-4), and collagen 1 alpha 1 (COL1A1), relative to PCL-DA scaffolds and osteogenic medium controls. Likewise, the expression of runt-related transcription factor 2 (RUNX2) and BMP-4 was elevated in the presence of PD-coating. In contrast, the chondrogenic and adipogenic responses associated with the scaffolds matched or were reduced relative to osteogenic medium controls, indicating that the scaffolds display intrinsic osteoinductivity.

摘要

工程化具有成骨诱导性、自适应性的支架为修复形状不规则的颅颌面骨缺损提供了一种潜在的治疗方法。最近,我们对具有成骨诱导性的聚(ε-己内酯)-二丙烯酸酯(PCL-DA)形状记忆聚合物(SMP)进行了创新,将聚 L-乳酸(PLLA)纳入 PCL-DA 网络中,形成半互穿网络(semi-IPN)。由这些 PCL-DA/PLLA 半互穿网络形成的支架的刚度在小梁骨的范围内,并相对于由缓慢降解的 PCL-DA SMP 形成的支架加速降解。在此,我们首次证明 PCL-DA/PLLA 半互穿网络 SMP 支架比 PCL-DA 具有更高的固有成骨诱导性。我们还证实,应用仿生聚多巴胺(PD)涂层进一步提高了这些 PCL-DA/PLLA 半互穿网络 SMP 的成骨诱导能力。在没有成骨补充剂的情况下,在 PCL-DA/PLLA 支架中培养的人间充质干细胞(h-MSCs)的蛋白水平评估显示,与 PCL-DA 支架和成骨培养基对照相比,成骨标志物osterix、骨形态发生蛋白 4(BMP-4)和胶原 1 型α 1(COL1A1)的表达增加。同样,在 PD 涂层存在的情况下,RUNX2 和 BMP-4 的表达升高。相比之下,支架的软骨形成和脂肪形成反应与成骨培养基对照相匹配或降低,表明支架具有内在的成骨诱导性。

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