Borgese Marina, Barone Ludovica, Rossi Federica, Raspanti Mario, Papait Roberto, Valdatta Luigi, Bernardini Giovanni, Gornati Rosalba
Department of Biotechnology and Life Sciences, University of Insubria, via J.H. Dunant 3, 21100 Varese, Italy.
Department of Medicine and Surgery, University of Insubria, Via Guicciardini 9, 21100 Varese, Italy.
Nanomaterials (Basel). 2020 Sep 12;10(9):1822. doi: 10.3390/nano10091822.
This work is addressed to provide, by experiments, results on the repercussion that a nanostructured scaffold could have on viability, differentiation and secretion of bioactive factors of human adipose-derived stem cells (hASCs) when used in association to promote angiogenesis, a crucial condition to favour tissue regeneration. To achieve this aim, we evaluated cell viability and morphology by MTT (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide) assay and microscopy analysis, respectively. We also investigated the expression of some of those genes involved in angiogenesis and differentiation processes utilizing quantitative polymerase chain reaction (qPCR), whereas the amounts of Vascular Endothelial Growth Factor A, Interleukin 6 and Fatty Acid-Binding Protein 4 secreted in the culture medium, were quantified by enzyme-linked immunosorbent assay (ELISA). Results suggested that, in the presence of the scaffold, cell proliferation and the exocytosis of factors involved in the angiogenesis process are reduced; by contrast, the expression of those genes involved in hASC differentiation appeared enhanced. To guarantee cell survival, the construct dimensions are, generally, smaller than clinically required. Furthermore, being the paracrine event the primary mechanism exerting the beneficial effects on injured tissues, the use of conditioned culture medium instead of cells may be convenient.
本研究旨在通过实验提供有关纳米结构支架在与促进血管生成相关联使用时,对人脂肪来源干细胞(hASC)的活力、分化及生物活性因子分泌的影响的结果,而血管生成是有利于组织再生的关键条件。为实现这一目标,我们分别通过MTT(3-[4,5-二甲基噻唑-2-基]-2,5-二苯基四氮唑溴盐)法和显微镜分析评估细胞活力和形态。我们还利用定量聚合酶链反应(qPCR)研究了一些参与血管生成和分化过程的基因的表达,而通过酶联免疫吸附测定(ELISA)对培养基中分泌的血管内皮生长因子A、白细胞介素6和脂肪酸结合蛋白4的量进行了定量。结果表明,在有支架存在的情况下,细胞增殖以及参与血管生成过程的因子的胞吐作用降低;相比之下,参与hASC分化的那些基因的表达似乎增强。为保证细胞存活,构建体尺寸通常小于临床所需。此外,由于旁分泌事件是对受损组织发挥有益作用的主要机制,使用条件培养基而非细胞可能会更方便。