Institute of Biomedical Engineering, Department for Medical Technologies and Regenerative Medicine, Eberhard Karls University Tübingen, Tübingen, Germany.
NMI Natural and Medical Sciences Institute at the University Tübingen, Reutlingen, Germany.
Tissue Eng Part C Methods. 2021 Nov;27(11):589-604. doi: 10.1089/ten.TEC.2021.0178.
In this study, we describe the production of hybrid gelatin-poly-L-lactide electrospun scaffolds whose hydrophilicity was controlled by binding increasing concentrations of hyaluronic acid (HA). We show that cross-linking has advantages over coating when aiming to functionalize the scaffolds with HA. The here described scaffolds structurely mimicked the complexity of the extracellular matrix, and when excited by second harmonic generation, they produced a signal that is typical of collagen-containing biological fibers. Fluorescence lifetime imaging microscopy (FLIM) was used to marker-independently monitor the growth of human dermal fibroblasts on the electrospun scaffolds using reduced (phosphorylated) nicotinamide adenine dinucleotide as target. Benefitting from the different fluorescence lifetimes of the polymer and the endogenous cellular fluorophore, we were able to distinguish and separate the signals produced by the cells from the signals generated by the electrospun scaffolds. FLIM further allowed the detection of metabolic differences in the cells seeded on the HA-functionalized scaffolds compared with cells that were cultured on nonfunctionalized control scaffolds.
在这项研究中,我们描述了混合明胶-聚-L-乳酸电纺支架的制备,通过结合不同浓度的透明质酸(HA)来控制其亲水性。我们表明,当目标是通过 HA 对支架进行功能化时,交联比涂层更有优势。这里描述的支架结构模拟了细胞外基质的复杂性,当受到二次谐波产生的激发时,它们产生了一种典型的含有胶原蛋白的生物纤维信号。荧光寿命成像显微镜(FLIM)被用于使用还原(磷酸化)烟酰胺腺嘌呤二核苷酸作为靶标,对人皮肤成纤维细胞在电纺支架上的生长进行无标记独立监测。受益于聚合物和内源性细胞荧光团的不同荧光寿命,我们能够区分和分离由细胞产生的信号与由电纺支架产生的信号。FLIM 进一步检测到在 HA 功能化支架上接种的细胞与在非功能化对照支架上培养的细胞之间的代谢差异。