细胞外基质纳米形貌对人牙干细胞生长特性和细胞形态变化的影响

V. Dhanvantri, R. Ramya, K. Cherian, Balasundari Ramesh
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引用次数: 0

摘要

目的:牙髓内牙干细胞生态位存在纳米形貌和可溶性细胞外因子。它们对牙干细胞存活和分化的影响尚未确定。本研究旨在分析细胞外基质(ECM)纳米形貌和血清(可溶性因子)对人牙髓干细胞(hDPSC)生长、分化潜能和形态特征的单独和联合作用。本研究旨在评估和比较hDPSC对不同环境信号(纳米纤维、血清和条件培养基)的反应。材料和方法:在本研究中,制备的聚乳酸纳米纤维被用作体外结构仿生体内ECM/干细胞生态位中天然纳米形貌的仿生材料。用血清和条件培养基作为体外模拟干细胞在体内暴露的可溶性因子。在存在和不存在可生物降解的聚l -乳酸纳米纤维和血清的情况下培养hDPSC。以细胞活力和每代翻倍时间为间隔评估hDPSC的生长特性。用倒置显微镜和H&E观察细胞形态学变化。作为研究的第二部分,将所有培养条件下的hDPSC暴露于牙髓条件培养基(DPCM)中3天。短暂暴露于DPCM后,观察hDPSC的生长特征和形态变化。此外,利用扫描电子显微镜对暴露在条件介质中的纳米纤维上的hDPSC进行形态学研究。采用qRT-PCR检测分化后的细胞中RUNX2、骨桥蛋白和β-微管蛋白III基因的神经源性和牙源性表达。结果:在纳米纤维和血清的作用下,hDPSC具有较好的增殖和存活能力。纳米纤维或血清的缺失极大地改变了干细胞的存活和增殖,也表明了分化。此外,我们观察到,短暂暴露于DPCM后,PLLA纳米纤维和血清的存在有利于更高的牙源性和神经源性分化潜力,而没有特征性的末梢分化形态学变化。结论:hDPSC具有从微环境中感知纳米级几何线索的能力。纳米形貌和细胞外基质的可溶性因子都影响hDPSC。进一步的研究是必要的,以确定在这种相互作用中起重要作用的关键途径。在纳米纤维和血清的存在下,hDPSC表现出更好的存活和增殖。纳米纤维或血清的缺失极大地改变了干细胞的存活和增殖,并显示出指示分化的变化。使用GraphPad Prism 5软件对结果进行比较分析。hDPSC具有从微环境中感知纳米级几何线索的能力。纳米形貌和细胞外基质的可溶性因子共同影响hDPSC的命运。进一步的研究是必要的,以确定在这种相互作用中起重要作用的关键途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of human dental stem cell growth characteristics and cellular morphological changes in response to extracellular matrix nanotopography
Objective: Nanotopography and soluble extracellular factors are present in the dental stem cell niche in the pulp. Their effect on dental stem cell survival and differentiation is yet to be established. We aimed to analyze the individual and combined roles of extracellular matrix (ECM) nanotopography and serum (soluble factors) on the growth, differentiation potential, and morphological characteristics of the human dental pulp stem cells (hDPSC). This study aimed to evaluate and compare the hDPSC response to different environmental cues – nanofibers, serum, and conditioned media. Materials and methods: In this study, fabricated PLLA nanofibers were used as the in vitro structural biomimetic of the native nanotopography found in the in vivo ECM/stem cell niche. Serum and conditioned media were used as the in vitro mimic of the soluble factors to which stem cells get exposed in vivo. hDPSC were grown in the presence and absence of biodegradablepoly-L-lactic-acid nanofibers and serum. The growth characteristics of hDPSC were assessed in terms of cell viability and doubling time at the interval of every passage. Cellular morphological changes were studied using inverted microscopy and H&E. As the second part of the study, hDPSC in all culture conditions were exposed to Dental Pulp Conditioned Media (DPCM) for a short duration of 3 days. After transient exposure to DPCM, the growth characteristics and the morphological changes of hDPSC were assessed. In addition, scanning electron microscopy was used for the morphological study of hDPSC on nanofibers, exposed to conditioned media. The differentiated cells were analyzed by qRT-PCR for neurogenic and odontogenic expression of RUNX2, osteopontin, and β-tubulin III genes. Results: hDPSC showed better survival and proliferation in the presence of nanofibers and serum. Absence of nanofibers or serum greatly altered stem cell survival and proliferation and also indicated differentiation. In addition, it was observed that after transient exposure to DPCM, the presence of both PLLA nanofiber and serum favoured higher odontogenic and neurogenic differentiation potential, without characteristic morphological changes of terminal differentiation. Conclusion: hDPSC has the ability to sense nanoscale geometric cues from their microenvironment. Nanotopography and soluble factors of the extracellular matrix both affect hDPSC. Further studies are essential to identify the key pathways that play a vital role in such interactions. The hDPSC demonstrated better survival and proliferation in the presence of nanofibers and serum. Absence of nanofibers or serum greatly altered stem cell survival and proliferation and also showed changes indicative of differentiation. The results were compared and analyzed using GraphPad Prism 5 Software. hDPSC possess the ability to sense nanoscale geometric cues from their microenvironment. Nanotopography and soluble factors of the Extracellular matrix together influence the fate of hDPSC. Further studies are essential to identify the key pathways that play a vital role in such interactions.
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