Walker Joseph C, Jorgensen Ashley M, Sarkar Anyesha, Gent Stephen P, Messerli Mark A
Department of Biology and Microbiology, South Dakota State University, Brookings, SD, United States.
Department of Mechanical Engineering, South Dakota State University, Brookings, SD, United States.
Front Bioeng Biotechnol. 2022 Sep 26;10:983317. doi: 10.3389/fbioe.2022.983317. eCollection 2022.
Electrical stimulation (ES) promotes healing of chronic epidermal wounds and delays degeneration of articular cartilage. Despite electrotherapeutic treatment of these non-excitable tissues, the mechanisms by which ES promotes repair are unknown. We hypothesize that a beneficial role of ES is dependent on electrokinetic perfusion in the extracellular space and that it mimics the effects of interstitial flow. , the extracellular space contains mixtures of extracellular proteins and negatively charged glycosaminoglycans and proteoglycans surrounding cells. While these anionic macromolecules promote water retention and increase mechanical support under compression, in the presence of ES they should also enhance electro-osmotic flow (EOF) to a greater extent than proteins alone. To test this hypothesis, we compare EOF rates between artificial matrices of gelatin (denatured collagen) with matrices of gelatin mixed with anionic polymers to mimic endogenous charged macromolecules. We report that addition of anionic polymers amplifies EOF and that a matrix comprised of 0.5% polyacrylate and 1.5% gelatin generates EOF with similar rates to those reported in cartilage. The enhanced EOF reduces mortality of cells at lower applied voltage compared to gelatin matrices alone. We also use modeling to describe the range of thermal changes that occur during these electrokinetic experiments and during electrokinetic perfusion of soft tissues. We conclude that the negative charge density of native extracellular matrices promotes electrokinetic perfusion during electrical therapies in soft tissues and may promote survival of artificial tissues and organs prior to vascularization and during transplantation.
电刺激(ES)可促进慢性表皮伤口愈合,并延缓关节软骨退变。尽管对这些非兴奋性组织进行了电治疗,但ES促进修复的机制尚不清楚。我们假设ES的有益作用依赖于细胞外空间的电动灌注,并且它模拟了间质流动的效果。细胞外空间包含细胞外蛋白质以及围绕细胞的带负电荷的糖胺聚糖和蛋白聚糖的混合物。虽然这些阴离子大分子促进水分保留并在压缩下增加机械支撑,但在存在ES的情况下,它们还应比单独的蛋白质更大程度地增强电渗流(EOF)。为了验证这一假设,我们比较了明胶(变性胶原蛋白)人工基质与混合了阴离子聚合物的明胶基质(以模拟内源性带电大分子)之间 的EOF速率。我们报告称,添加阴离子聚合物可放大EOF,并且由0.5%聚丙烯酸酯和1.5%明胶组成的基质产生的EOF速率与软骨中报道的速率相似。与单独的明胶基质相比,增强的EOF在较低施加电压下降低了细胞死亡率。我们还使用模型来描述在这些电动实验以及软组织电动灌注过程中发生的热变化范围。我们得出结论,天然细胞外基质的负电荷密度在软组织电治疗过程中促进电动灌注,并可能在血管化之前和移植期间促进人工组织和器官的存活。