Hashmi Basma, Mammoto Tadanori, Weaver James, Ferrante Thomas, Jiang Amanda, Jiang Elisabeth, Feliz Juani, Ingber Donald E
Vascular Biology Program and Department of Surgery, Boston Children's Hospital and Harvard Medical School, Boston, MA 02115, USA.
Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02115, USA.
Stem Cell Res. 2017 Oct;24:55-60. doi: 10.1016/j.scr.2017.08.011. Epub 2017 Aug 17.
Tooth formation during embryogenesis is controlled through a complex interplay between mechanical and chemical cues. We have previously shown that physical cell compaction of dental mesenchyme cells during mesenchymal condensation is responsible for triggering odontogenic differentiation during embryogenesis, and that expression of Collagen VI stabilizes this induction. In addition, we have shown that synthetic polymer scaffolds that artificially induce cell compaction can induce embryonic mandible mesenchymal cells to initiate tooth differentiation both in vitro and in vivo. As embryonic cells would be difficult to use for regenerative medicine applications, here we explored whether compressive scaffolds coated with Collagen VI can be used to induce adult bone marrow stromal cells (BMSCs) to undergo an odontogenic lineage switch. These studies revealed that when mouse BMSCs are compressed using these scaffolds they increase expression of critical markers of tooth differentiation in vitro, including the key transcription factors Pax9 and Msx1. Implantation under the kidney capsule of contracting scaffolds bearing these cells in mice also resulted in local mineralization, calcification and production of dentin-like tissue. These findings show that these chemically-primed compressive scaffolds can be used to induce adult BMSCs to undergo a lineage switch and begin to form dentin-like tissue, thus raising the possibility of using adult BMSCs for future tooth regeneration applications.
胚胎发育过程中的牙齿形成是通过机械信号和化学信号之间复杂的相互作用来控制的。我们之前已经表明,间充质凝聚过程中牙间充质细胞的物理性细胞压实负责在胚胎发育过程中触发牙源性分化,并且胶原蛋白VI的表达稳定了这种诱导作用。此外,我们还表明,人工诱导细胞压实的合成聚合物支架能够在体外和体内诱导胚胎下颌间充质细胞启动牙齿分化。由于胚胎细胞难以用于再生医学应用,因此我们在此探讨了涂有胶原蛋白VI的压缩支架是否可用于诱导成年骨髓基质细胞(BMSC)发生牙源性谱系转换。这些研究表明,当使用这些支架对小鼠BMSC进行压缩时,它们会在体外增加牙齿分化关键标志物的表达,包括关键转录因子Pax9和Msx1。将携带这些细胞的收缩支架植入小鼠肾囊下也会导致局部矿化、钙化以及牙本质样组织的产生。这些发现表明,这些化学预处理的压缩支架可用于诱导成年BMSC发生谱系转换并开始形成牙本质样组织,从而增加了将成年BMSC用于未来牙齿再生应用的可能性。