Department of Biomedical Sciences, Texas A&M University College of Dentistry, Dallas, Texas 75246, United States.
ACS Appl Mater Interfaces. 2022 Aug 17;14(32):36451-36461. doi: 10.1021/acsami.2c09420. Epub 2022 Aug 7.
Periodontal ligament (PDL) is assembled from highly organized collagen fiber bundles (PDL principal fibers) that are crucial in supporting teeth and buffering mechanical force. Therefore, regeneration of PDL needs to reconstruct these well-ordered fiber bundles to restore PDL functions. However, the formation of PDL principal fibers has long been a challenge due to the absence of an effective three-dimensional (3D) matrix to guide the growth of periodontal ligament stem cells (PDLSCs) and to inhibit the osteogenic differentiation of PDLSCs during the PDL principal fibers deposition. In this work, we designed and fabricated a bio-inspired tubular 3D matrix to guide the migration and growth of human PDLSCs and form well-aligned PDL principal fibers. As a biomimetic 3D template, the tubular matrix controlled PDLSCs migration inside the tubules and aligned the cells to the designated direction. Inside the tubular matrix, the PDLSCs expressed PDL markers and formed oriented fiber bundles with the same size and density as those of natural PDL principal fibers. Furthermore, the tubular matrix downregulated the osteogenic differentiation of PDLSCs. A mechanism study revealed that the Yap1/Twist1 signaling pathway was involved in the inhibition of PDLSCs osteogenesis within the tubular matrix. This work provides an effective approach to induce PDLSCs to form principal fibers and gives insight into the underlying mechanism of inhibiting the osteogenic differentiation of PDLSCs in biomimetic tubular matrices.
牙周韧带(PDL)由高度有序的胶原纤维束(PDL 主纤维)组成,对于支撑牙齿和缓冲机械力至关重要。因此,牙周韧带的再生需要重建这些有序的纤维束,以恢复牙周韧带的功能。然而,由于缺乏有效的三维(3D)基质来指导牙周韧带干细胞(PDLSCs)的生长并抑制 PDLSCs 在 PDL 主纤维沉积过程中的成骨分化,PDL 主纤维的形成一直是一个挑战。在这项工作中,我们设计并制造了一种仿生管状 3D 基质,以指导人牙周韧带干细胞的迁移和生长,并形成排列整齐的 PDL 主纤维。作为一种仿生 3D 模板,管状基质控制着 PDLSCs 在管内的迁移,并将细胞排列到指定的方向。在管状基质内,PDLSCs 表达 PDL 标志物,并形成与天然 PDL 主纤维具有相同大小和密度的定向纤维束。此外,管状基质下调了 PDLSCs 的成骨分化。机制研究表明,Yap1/Twist1 信号通路参与了管状基质内 PDLSCs 成骨的抑制。这项工作为诱导 PDLSCs 形成主纤维提供了一种有效的方法,并深入了解了在仿生管状基质中抑制 PDLSCs 成骨分化的潜在机制。