Differential proteomics profile of microcapillary networks in response to sound pattern-driven local cell density enhancement

Q3 Biochemistry, Genetics and Molecular Biology Biomaterials and biosystems Pub Date : 2024-03-29 DOI:10.1016/j.bbiosy.2024.100094
N. Di Marzio , R. Tognato , E. Della Bella , V. De Giorgis , M. Manfredi , A. Cochis , M. Alini , T. Serra
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Abstract

Spatial cell organization and biofabrication of microcapillary networks in vitro has a great potential in tissue engineering and regenerative medicine. This study explores the impact of local cell density enhancement achieved through an innovative sound-based patterning on microcapillary networks formation and their proteomic profile. Human umbilical vein endothelial cells (HUVEC) and human pericytes from placenta (hPC-PL) were mixed in a fibrin suspension. The mild effect of sound-induced hydrodynamic forces condensed cells into architected geometries showing good fidelity to the numerical simulation of the physical process. Local cell density increased significantly within the patterned areas and the capillary-like structures formed following the cell density gradient. Over five days, these patterns were well-maintained, resulting in concentric circles and honeycomb-like structures.

Proteomic analysis of the pre-condensed cells cultured for 5 days, revealed over 900 differentially expressed proteins when cells were preassembled through mild-hydrodynamic forces. Gene ontology (GO) enrichment analysis identified cellular components, molecular functions, and biological processes that were up- and down-regulated, providing insights regarding molecular processes influenced by the local density enhancement. Furthermore, we employed Ingenuity Pathway Analysis (IPA) to identify altered pathways and predict upstream regulators. Notably, VEGF-A emerged as one of the most prominent upstream regulators.

Accordingly, this study initiates the unraveling of the changes in microcapillary networks at both molecular and proteins level induced by cell condensation obtained through sound patterning. The findings provide valuable insights for further investigation into sound patterning as a biofabrication technique for creating more complex microcapillary networks and advancing in vitro models.

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微毛细血管网络对声音模式驱动的局部细胞密度增强的差异蛋白质组学特征
体外微毛细血管网络的空间细胞组织和生物制造在组织工程和再生医学中具有巨大潜力。本研究探讨了通过创新的声基图案化技术提高局部细胞密度对微毛细血管网络形成及其蛋白质组谱的影响。研究人员将人脐静脉内皮细胞(HUVEC)和人胎盘周细胞(hPC-PL)混合在纤维蛋白悬浮液中。声音引起的流体动力的轻微影响将细胞凝聚成结构化的几何图形,与物理过程的数值模拟显示出良好的保真度。图案区域内的局部细胞密度明显增加,毛细管样结构随细胞密度梯度而形成。对培养了 5 天的预凝聚细胞进行的蛋白质组分析表明,当细胞通过温和的流体动力进行预组装时,有 900 多种不同表达的蛋白质。基因本体(GO)富集分析确定了上调和下调的细胞成分、分子功能和生物过程,为了解受局部密度增强影响的分子过程提供了见解。此外,我们还采用了 Ingenuity Pathway Analysis(IPA)来识别改变的通路并预测上游调节因子。因此,这项研究开始从分子和蛋白质两个层面揭示通过声音模式化获得的细胞凝聚所诱导的微毛细血管网络的变化。这些发现为进一步研究声音图案化作为一种生物制造技术,创造更复杂的微毛细血管网络和推进体外模型提供了宝贵的见解。
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