Neural growth patterns: how random and aligned fibers guide 3D cell organization and pseudospheroid formation.

IF 4.8 3区 工程技术 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Frontiers in Bioengineering and Biotechnology Pub Date : 2025-10-03 eCollection Date: 2025-01-01 DOI:10.3389/fbioe.2025.1659965
Jana Hlinkova, Karolina Dziemidowicz, Mathilde M Ullrich, Anne Eriksson Agger, Aina-Mari Lian, Janne Elin Reseland, Athina Samara
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引用次数: 0

Abstract

Background and purpose: Electrospun biomaterials replicate the structural complexity of the extracellular matrix (ECM), providing mechanical support and promoting neural cell survival and organization. Fiber orientation is a key determinant of neural cell behavior, influencing adhesion, migration, and differentiation. This study investigates how high seeding density combined with fiber directionality shapes SH-SY5Y culture morphology, gene expression, and early network formation; all critical factors for the design of next-generation scaffolds for neural tissue engineering.

Methods: Polycaprolactone (PCL) scaffolds with either random or aligned fiber orientation were fabricated via monoaxial electrospinning. Human SH-SY5Y neuroblastoma cells were seeded at high density and cultured for 7 days, and cell viability was assessed by lactate dehydrogenase (LDH) activity. Neural, ECM, and differentiation markers were analyzed using quantitative PCR, Luminex cytokine profiling, and confocal immunofluorescence.

Results: Hydrophobic PCL fibers supported cell adhesion, migration, and proliferation when cells were seeded in small clusters. After 7 days, cell coverage of the fiber-mat was significantly higher on random fibers compared to aligned ones (27.7% vs. 15.8%). Fiber orientation influenced both culture morphology and gene expression. Pseudospheroids formed on both substrates, that differed in perimeter (348.5 µm on random vs. 450.5 µm on aligned fibers, p < 0.05), with no significant difference in thickness (38.4 ± 7.7 µm vs. 43.2 ± 5.5 µm). mRNA expression of connexin 43 and β3-tubulin increased significantly from day 1 to day 7 on random fibers. On aligned fibers, mRNA patterns resembled cells cultured on glass (control), with elevated connexin 31 and doublecortin over time. Immunofluorescence showed early enrichment of nestin on aligned fibers (day 1), and greater expression of β3-tubulin, acetylated tubulin, and connexin 31 on aligned substrates, whereas fibronectin 1 was more prominent on random fibers.

Conclusion: Fiber orientation significantly affected SH-SY5Y cell behaviour, including adhesion, formation of pseudospheroids, and differentiation marker expression under high-density conditions. Random and aligned fibers elicited distinct structural patterns and molecular responses, highlighting the importance of scaffold architecture in the rational design of neuroregenerative platforms. To our knowledge, this is the first study to describe scaffold-anchored neural pseudospheroids as a distinct model from conventional suspension spheroids.

神经生长模式:随机和排列的纤维如何引导三维细胞组织和假球体形成。
背景与目的:电纺丝生物材料复制细胞外基质(ECM)结构的复杂性,提供机械支持,促进神经细胞的存活和组织。纤维取向是神经细胞行为的关键决定因素,影响粘附、迁移和分化。本研究探讨了高播种密度和纤维方向性对SH-SY5Y培养形态、基因表达和早期网络形成的影响;这些都是设计下一代神经组织工程支架的关键因素。方法:采用单轴静电纺丝法制备纤维取向随机或排列的聚己内酯(PCL)支架。高密度播种人SH-SY5Y神经母细胞瘤细胞,培养7天,采用乳酸脱氢酶(LDH)活性测定细胞活力。使用定量PCR、Luminex细胞因子谱和共聚焦免疫荧光分析神经、ECM和分化标志物。结果:疏水性PCL纤维支持细胞的粘附、迁移和增殖。7天后,纤维垫在随机纤维上的细胞覆盖率显著高于排列纤维(27.7% vs. 15.8%)。纤维取向影响培养形态和基因表达。在两种基质上形成假球体,其周长不同(随机纤维为348.5µm,排列纤维为450.5µm, p < 0.05),厚度无显著差异(38.4±7.7µm vs. 43.2±5.5µm)。连接蛋白43和β3-微管蛋白mRNA在随机纤维上的表达从第1天到第7天显著增加。在排列的纤维上,mRNA模式类似于在玻璃(对照)上培养的细胞,随着时间的推移,连接蛋白31和双皮质素升高。免疫荧光显示,巢蛋白在排列的纤维上较早富集(第1天),β3-微管蛋白、乙酰化微管蛋白和连接蛋白31在排列的底物上表达较多,而纤维连接蛋白1在随机纤维上表达较多。结论:高密度条件下,纤维取向显著影响SH-SY5Y细胞的粘附、假球体的形成和分化标记的表达。随机和排列的纤维引发了不同的结构模式和分子反应,突出了支架结构在合理设计神经再生平台中的重要性。据我们所知,这是第一个将支架锚定神经假球体描述为与传统悬浮球体不同的模型的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Frontiers in Bioengineering and Biotechnology
Frontiers in Bioengineering and Biotechnology Chemical Engineering-Bioengineering
CiteScore
8.30
自引率
5.30%
发文量
2270
审稿时长
12 weeks
期刊介绍: The translation of new discoveries in medicine to clinical routine has never been easy. During the second half of the last century, thanks to the progress in chemistry, biochemistry and pharmacology, we have seen the development and the application of a large number of drugs and devices aimed at the treatment of symptoms, blocking unwanted pathways and, in the case of infectious diseases, fighting the micro-organisms responsible. However, we are facing, today, a dramatic change in the therapeutic approach to pathologies and diseases. Indeed, the challenge of the present and the next decade is to fully restore the physiological status of the diseased organism and to completely regenerate tissue and organs when they are so seriously affected that treatments cannot be limited to the repression of symptoms or to the repair of damage. This is being made possible thanks to the major developments made in basic cell and molecular biology, including stem cell science, growth factor delivery, gene isolation and transfection, the advances in bioengineering and nanotechnology, including development of new biomaterials, biofabrication technologies and use of bioreactors, and the big improvements in diagnostic tools and imaging of cells, tissues and organs. In today`s world, an enhancement of communication between multidisciplinary experts, together with the promotion of joint projects and close collaborations among scientists, engineers, industry people, regulatory agencies and physicians are absolute requirements for the success of any attempt to develop and clinically apply a new biological therapy or an innovative device involving the collective use of biomaterials, cells and/or bioactive molecules. “Frontiers in Bioengineering and Biotechnology” aspires to be a forum for all people involved in the process by bridging the gap too often existing between a discovery in the basic sciences and its clinical application.
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