Center for Biomedical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.
PLoS One. 2010 Apr 22;5(4):e10305. doi: 10.1371/journal.pone.0010305.
We here report the development of two peptide scaffolds designed for periodontal ligament fibroblasts. The scaffolds consist of one of the pure self-assembling peptide scaffolds RADA16 through direct coupling to short biologically active motifs. The motifs are 2-unit RGD binding sequence PRG (PRGDSGYRGDS) and laminin cell adhesion motif PDS (PDSGR). RGD and laminin have been previously shown to promote specific biological activities including periodontal ligament fibroblasts adhesion, proliferation and protein production. Compared to the pure RADA16 peptide scaffold, we here show that these designer peptide scaffolds significantly promote human periodontal ligament fibroblasts to proliferate and migrate into the scaffolds (for approximately 300 microm/two weeks). Moreover these peptide scaffolds significantly stimulated periodontal ligament fibroblasts to produce extracellular matrix proteins without using extra additional growth factors. Immunofluorescent images clearly demonstrated that the peptide scaffolds were almost completely covered with type I and type III collagens which were main protein components of periodontal ligament. Our results suggest that these designer self-assembling peptide nanofiber scaffolds may be useful for promoting wound healing and especially periodontal ligament tissue regeneration.
我们在此报告了两种专为牙周韧带成纤维细胞设计的肽支架的开发。这些支架由一种纯自组装肽支架 RADA16 通过直接偶联到短的生物活性基序组成。这些基序是 2 个单位的 RGD 结合序列 PRG(PRGDSGYRGDS)和层粘连蛋白细胞黏附基序 PDS(PDSGR)。RGD 和层粘连蛋白先前已被证明可促进特定的生物活性,包括牙周韧带成纤维细胞的黏附、增殖和蛋白质产生。与纯 RADA16 肽支架相比,我们在此表明,这些设计肽支架可显著促进人牙周韧带成纤维细胞增殖并迁移到支架中(大约 300 微米/两周)。此外,这些肽支架可显著刺激牙周韧带成纤维细胞产生细胞外基质蛋白,而无需使用额外的生长因子。免疫荧光图像清楚地表明,肽支架几乎完全被 I 型和 III 型胶原覆盖,胶原是牙周韧带的主要蛋白成分。我们的结果表明,这些设计的自组装肽纳米纤维支架可能有助于促进伤口愈合,特别是牙周韧带组织再生。