地形和化学诱导线索协同促进排列牙髓干细胞片的雪旺细胞分化

IF 3.1 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Journal of Tissue Engineering and Regenerative Medicine Pub Date : 2023-07-18 DOI:10.1155/2023/7958770
M. Drewry, K. Rothermund, F. Syed-Picard
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引用次数: 0

摘要

周围神经具有固有的再生能力,但这些雪旺细胞介导的机制不足以治疗严重损伤。在目前的临床治疗中,缓慢的再生和异常的神经再生导致了较差的功能预后。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,即刺激轴突再生的生长因子。在此之前,我们已经证实DPSCs可以产生具有线性排列的细胞外基质(ECM)的无支架片。这些片材通过DPSCs提供营养线索,通过排列的ECM提供定向线索,加速轴突的生长,从而提供一种能够解决当前临床挑战的生物材料。DPSCs具有向雪旺细胞(SC-DPSCs)分化的倾向,进一步增强其内源性NTF表达。在这里,我们评估了诱导SC分化对我们的DPSC片神经再生生物活性的影响。这些薄片在有线性微槽的基底上形成,以指导细胞沉积排列的ECM。与未对齐的uDPSC片相比,使用SC分化培养基(SCDM)诱导分化使NTF表达增加了2倍,而在线性取向的SC- dpsc片中,这种效果被放大了多达8倍。此外,这些排列的SC-DPSC薄片重塑了ECM薄片,以更接近地模拟再生神经微环境,分别比未排列的uDPSC薄片表达8倍和2 × 107倍的胶原IV和层粘连蛋白。这些数据表明,SCDM的化学信号和排列细胞片的机械转导信号协同增强了DPSCs向修复sc样细胞的分化。为了评估其对神经细胞发生的功能影响,我们将DPSC片与神经分化的神经母细胞瘤SH-SY5Y细胞直接共培养。在这个体外培养系统中,排列的SC-DPSC片促进了定向的神经突样生长,类似于排列的未诱导的DPSC片,并增加了侧支分支,这可能与自然sc介导的修复过程相关。因此,线性排列的SC-DPSC片具有促进神经再生和减少异常神经再生的潜力,从而为改善周围神经损伤的治疗提供了一种有前景的生物材料。
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Topographical and Chemical Inductive Cues Synergistically Enhance the Schwann Cell Differentiation of Aligned Dental Pulp Stem Cell Sheets
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 × 107-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 in vitro 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.
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来源期刊
CiteScore
7.50
自引率
3.00%
发文量
97
审稿时长
4-8 weeks
期刊介绍: Journal of Tissue Engineering and Regenerative Medicine publishes rapidly and rigorously peer-reviewed research papers, reviews, clinical case reports, perspectives, and short communications on topics relevant to the development of therapeutic approaches which combine stem or progenitor cells, biomaterials and scaffolds, growth factors and other bioactive agents, and their respective constructs. All papers should deal with research that has a direct or potential impact on the development of novel clinical approaches for the regeneration or repair of tissues and organs. The journal is multidisciplinary, covering the combination of the principles of life sciences and engineering in efforts to advance medicine and clinical strategies. The journal focuses on the use of cells, materials, and biochemical/mechanical factors in the development of biological functional substitutes that restore, maintain, or improve tissue or organ function. The journal publishes research on any tissue or organ and covers all key aspects of the field, including the development of new biomaterials and processing of scaffolds; the use of different types of cells (mainly stem and progenitor cells) and their culture in specific bioreactors; studies in relevant animal models; and clinical trials in human patients performed under strict regulatory and ethical frameworks. Manuscripts describing the use of advanced methods for the characterization of engineered tissues are also of special interest to the journal readership.
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