Drewry Michelle D, Rothermund Kristi, Syed-Picard Fatima N
Department of Bioengineering, Swanson School of Engineering, University of Pittsburgh, Pittsburgh, PA, USA.
Center for Craniofacial Regeneration, School of Dental Medicine, University of Pittsburgh, Pittsburgh, PA, USA.
J Tissue Eng Regen Med. 2023 Jul 18;2023:7958770. doi: 10.1155/2023/7958770. eCollection 2023.
Peripheral nerves have an inherent capacity for regeneration, but these Schwann cell-mediated mechanisms are insufficient for severe injuries. With current clinical treatments, slow regeneration and aberrant reinnervation result in poor functional outcomes. Dental pulp stem cells (DPSCs) offer a promising source of therapeutic neurotrophic factors (NTFs), growth factors that stimulate axon regeneration. Previously, we established that DPSCs can generate scaffold-free sheets with a linearly aligned extracellular matrix (ECM). These sheets provide trophic cues via the DPSCs and directional cues through the aligned ECM to both accelerate and orient axon outgrowth, thus providing a biomaterial capable of addressing the current clinical challenges. DPSCs have a propensity for differentiating into Schwann cells (SC-DPSCs), further enhancing their endogenous NTF expression. Here, we evaluated the effect of inducing SC differentiation on the neuroregenerative bioactivity of our DPSC sheets. These sheets were formed on substrates with linear microgrooves to direct the cells to deposit an aligned ECM. Inducing differentiation using an SC differentiation medium (SCDM) increased NTF expression 2-fold compared to unaligned uDPSC sheets, and this effect was amplified in linearly oriented SC-DPSC sheets by up to 8-fold. Furthermore, these aligned SC-DPSC sheets remodeled the sheet ECM to more closely emulate a regenerative neural microenvironment, expressing 8-fold and 2 × 10-fold more collagen IV and laminin, respectively, than unaligned uDPSC sheets. These data demonstrate that the chemical cues of the SCDM and the mechanotransductive cues of the aligned cell sheet synergistically enhanced the differentiation of DPSCs into repair SC-like cells. To evaluate their functional effects on neuritogenesis, the DPSC sheets were directly cocultured with neuronally differentiated neuroblastoma SH-SY5Y cells. In this culture system, the aligned SC-DPSC sheets promoted oriented neurite-like outgrowth similar to aligned uninduced DPSC sheets and increased collateral branching, which may emulate stages associated with natural SC-mediated repair processes. Therefore, linearly aligned SC-DPSC sheets have the potential to both promote nerve regeneration and reduce aberrant reinnervation, thus providing a promising biomaterial for applications to improve the treatment of peripheral nerve injury.
周围神经具有内在的再生能力,但这些由施万细胞介导的机制对于严重损伤而言并不充分。在目前的临床治疗中,再生缓慢和异常再支配导致功能预后不佳。牙髓干细胞(DPSCs)提供了一种有前景的治疗性神经营养因子(NTFs)来源,神经营养因子是刺激轴突再生的生长因子。此前,我们证实DPSCs能够生成具有线性排列细胞外基质(ECM)的无支架薄片。这些薄片通过DPSCs提供营养信号,并通过排列的ECM提供定向信号,以加速和引导轴突生长,从而提供一种能够应对当前临床挑战的生物材料。DPSCs有分化为施万细胞(SC-DPSCs)的倾向,这进一步增强了它们内源性神经营养因子的表达。在此,我们评估了诱导施万细胞分化对我们的DPSC薄片神经再生生物活性的影响。这些薄片在具有线性微槽的底物上形成,以引导细胞沉积排列的ECM。与未排列的uDPSC薄片相比,使用施万细胞分化培养基(SCDM)诱导分化使神经营养因子表达增加了2倍,并且这种效应在线性排列的SC-DPSC薄片中放大了多达8倍。此外,这些排列的SC-DPSC薄片重塑了薄片ECM,使其更紧密地模拟再生神经微环境,与未排列的uDPSC薄片相比,分别表达多8倍和2×10倍的IV型胶原蛋白和层粘连蛋白。这些数据表明,SCDM的化学信号和排列的细胞薄片的机械转导信号协同增强了DPSCs向修复性施万细胞样细胞的分化。为了评估它们对神经突生长的功能影响,将DPSC薄片与神经元分化的神经母细胞瘤SH-SY5Y细胞直接共培养。在这个培养系统中,排列的SC-DPSC薄片促进了类似于排列的未诱导DPSC薄片的定向神经突样生长,并增加了侧支分支,这可能模拟了与天然施万细胞介导的修复过程相关的阶段。因此,线性排列的SC-DPSC薄片既有促进神经再生又有减少异常再支配的潜力,从而为改善周围神经损伤治疗的应用提供了一种有前景的生物材料。