Department of Biomedical Sciences, Texas A&M University College of Dentistry, Dallas, Texas 75246, United States.
ACS Appl Mater Interfaces. 2020 Dec 9;12(49):54481-54488. doi: 10.1021/acsami.0c17730. Epub 2020 Nov 30.
Dental pulp stem cells (DPSCs) are the primary stem cell source for regenerative endodontics. DPSCs need to undergo a polarization process and retain the permanent polarization status to perform the function of odontoblasts. However, the factors that control DPSC polarization and its underlying mechanism remain unknown. In this study, we established a unique nanofibrous tubular three-dimensional (3D) platform to explore DPSC polarization. The 3D platform has a "clean" background and confines one single DPSC in each microisland of the platform; therefore, it is capable of deciphering any signal that initiates or regulates DPSC polarization. Using the biomimetic platform, we identified that the nanofibrous tubular architecture is the crucial factor to initiate DPSC polarization. Dynamic morphological observation showed that the cellular process of the polarized DPSCs continuously extended and reached a plateau at 72 h. Meanwhile, Golgi apparatus, a cell polarization marker, continuously moved from a juxtanuclear region, passed the nucleus, and eventually settled down at a final position that was a few micrometers away from the nucleus. Inhibition of microfilament and microtubule polymerization demonstrated the indispensable role of cytoskeleton reorganization in modulating DPSC polarization. In addition, cell tension was involved in the regulation of DPSC polarization. The findings of this work expand the in-depth understanding of DPSC polarization, which helps design new bioinspired materials for regenerative endodontics.
牙髓干细胞(DPSCs)是再生牙髓学的主要干细胞来源。DPSCs 需要经历极化过程并保持永久极化状态才能发挥成牙本质细胞的功能。然而,控制 DPSC 极化的因素及其潜在机制尚不清楚。在这项研究中,我们建立了一个独特的纳米纤维管状三维(3D)平台来探索 DPSC 极化。该 3D 平台具有“干净”的背景,将每个微岛上的单个 DPSCs 限制在微岛上;因此,它能够破译任何启动或调节 DPSC 极化的信号。使用仿生平台,我们确定纳米纤维管状结构是启动 DPSC 极化的关键因素。动态形态观察表明,极化 DPSCs 的细胞过程不断延伸,在 72 小时达到平台期。同时,高尔基体是细胞极化的标志物,从核周区域不断移动,穿过核,并最终在离核几微米的最终位置定居。微丝和微管聚合的抑制表明细胞骨架重排在调节 DPSC 极化中的不可或缺作用。此外,细胞张力参与 DPSC 极化的调节。这项工作的发现扩展了对 DPSC 极化的深入理解,有助于为再生牙髓学设计新的仿生材料。