Arany P R, Huang G X, Gadish O, Feliz J, Weaver J C, Kim J, Yuen W W, Mooney D J
Harvard School of Engineering and Applied Sciences, Cambridge, MA, USA Wyss Institute for Biologically Inspired Engineering, Harvard University, Cambridge, MA, USA Harvard School of Dental Medicine, Boston, MA, USA National Institute of Dental and Craniofacial Research, Bethesda, MD, USA.
Harvard School of Engineering and Applied Sciences, Cambridge, MA, USA.
J Dent Res. 2014 Dec;93(12):1250-7. doi: 10.1177/0022034514542272. Epub 2014 Aug 20.
Tissue loss due to oral diseases requires the healing and regeneration of tissues of multiple lineages. While stem cells are native to oral tissues, a current major limitation to regeneration is the ability to direct their lineage-specific differentiation. This work utilizes polymeric scaffold systems with spatiotemporally controlled morphogen cues to develop precise morphogen fields to direct mesenchymal stem cell differentiation. First, a simple three-layer scaffold design was developed that presented two spatially segregated, lineage-specific cues (Dentinogenic TGF-β1 and Osteogenic BMP4). However, this system resulted in diffuse morphogen fields, as assessed by the in vitro imaging of cell-signaling pathways triggered by the morphogens. Mathematical modeling was then exploited, in combination with incorporation of specific inhibitors (neutralizing antibodies or a small molecule kinase inhibitor) into each morphogen in an opposing spatial pattern as the respective morphogen, to design a five-layer scaffold that was predicted to yield distinct, spatially segregated zones of morphogen signaling. To validate this system, undifferentiated MSCs were uniformly seeded in these scaffold systems, and distinct mineralized tissue differentiation were noted within these morphogen zones. Finally, to demonstrate temporal control over morphogen signaling, latent TGF-β1 was incorporated into one region of a concentric scaffold design, and laser treatment was used to activate the morphogen on-demand and to induce dentin differentiation solely within that specific spatial zone. This study demonstrates a significant advance in scaffold design to generate precise morphogen fields that can be used to develop in situ models to explore tissue differentiation and may ultimately be useful in engineering multi-lineage tissues in clinical dentistry.
口腔疾病导致的组织缺损需要多种谱系组织的愈合和再生。虽然干细胞存在于口腔组织中,但目前再生的一个主要限制是引导其谱系特异性分化的能力。这项工作利用具有时空控制形态发生素线索的聚合物支架系统来开发精确的形态发生素场,以引导间充质干细胞分化。首先,开发了一种简单的三层支架设计,该设计呈现了两种空间隔离的、谱系特异性线索(牙本质生成性转化生长因子-β1和成骨性骨形态发生蛋白4)。然而,通过对由形态发生素触发的细胞信号通路的体外成像评估,该系统导致了扩散的形态发生素场。然后利用数学建模,并将特定抑制剂(中和抗体或小分子激酶抑制剂)以与各自形态发生素相反的空间模式掺入每种形态发生素中,设计了一种五层支架,预计该支架将产生不同的、空间隔离的形态发生素信号区。为了验证该系统,将未分化的间充质干细胞均匀接种在这些支架系统中,并在这些形态发生素区内观察到了明显的矿化组织分化。最后,为了证明对形态发生素信号的时间控制,将潜伏性转化生长因子-β1掺入同心支架设计的一个区域,并使用激光处理按需激活形态发生素,仅在该特定空间区域内诱导牙本质分化。这项研究表明,在支架设计方面取得了重大进展,能够生成精确的形态发生素场,可用于开发原位模型以探索组织分化,并最终可能在临床牙科的多谱系组织工程中发挥作用。