Department of Periodontics and Oral Medicine, University of Michigan School of Dentistry, 1011 N. University Ave., Ann Arbor, MI, 48109, USA.
Department of Biomedical Engineering, University of Michigan College of Engineering, 1101 Beal Ave., Ann Arbor, MI, 48109, USA.
Adv Healthc Mater. 2018 Nov;7(22):e1800750. doi: 10.1002/adhm.201800750. Epub 2018 Oct 19.
Periodontal disease destroys supporting structures of teeth. However, tissue engineering strategies offer potential to enhance regeneration. Here, the strategies of patterned topography, spatiotemporally controlled growth factor gene delivery, and cell-based therapy to repair bone-periodontal ligament (PDL) interfaces are combined. Micropatterned scaffolds are fabricated for the ligament regions using polycaprolactone (PCL)/polylactic-co-glycolic acid and combined with amorphous PCL scaffolds for the bone region. Scaffolds are modified using chemical vapor deposition, followed by spatially controlled immobilization of vectors encoding either platelet-derived growth factor-BB or bone morphogenetic protein-7, respectively. The scaffolds are seeded with human cells and delivered to large alveolar bone defects in athymic rats. The effects of dual and single gene delivery with and without micropatterning are assessed after 3, 6, and 9 weeks. Gene delivery results in greater bone formation at three weeks. Micropatterning results in regenerated ligamentous tissues similar to native PDL. The combination results in more mature expression of collagen III and periostin, and with elastic moduli of regenerated tissues that are statistically indistinguishable from those of native tissue, while controls are less stiff than native tissues. Thus, controlled scaffold microtopography combined with localized growth factor gene delivery improves the regeneration of periodontal bone-PDL interfaces.
牙周病破坏了牙齿的支持组织。然而,组织工程策略提供了增强再生的潜力。在这里,将图案化形貌、时空控制的生长因子基因传递和基于细胞的治疗策略结合起来,用于修复骨-牙周韧带(PDL)界面。使用聚己内酯(PCL)/聚乳酸-共-羟基乙酸为韧带区域制造微图案化支架,并与无定形 PCL 支架结合用于骨区域。支架通过化学气相沉积进行修饰,然后分别通过空间控制固定编码血小板衍生生长因子-BB 或骨形态发生蛋白-7 的载体。将支架接种人类细胞并递送至无胸腺大鼠的大牙槽骨缺损中。在 3、6 和 9 周后评估双基因和单基因传递以及微图案化的效果。基因传递导致 3 周时骨形成增加。微图案化导致再生的韧带组织类似于天然 PDL。组合结果导致胶原 III 和骨桥蛋白的表达更成熟,并且再生组织的弹性模量与天然组织统计学上无差异,而对照组织比天然组织更柔软。因此,控制支架微形貌结合局部生长因子基因传递可改善牙周骨-PDL 界面的再生。