预分化皮肤样细胞可减轻体外烧伤

Ruhma Mahmood, Mahmood S Choudhery, Shaheen N. Khan, S. Riazuddin
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摘要

考虑到干细胞治疗对伤口愈合的重要性,我们之前已经建立了将干细胞(从胎盘中分离出来)成功分化为皮肤样细胞(角质形成细胞和成纤维细胞)的方案。在目前的研究中,我们旨在通过体外烧伤模型评估预分化皮肤样细胞对伤口愈合潜力的影响。从羊膜和脐带组织中获得羊膜上皮细胞(AECs)和脐带间充质干细胞(UCMSCs);分别分化为皮肤样细胞(角质细胞和成纤维细胞)。为了制备体外烧伤模型,从大鼠体内分离角质形成细胞和成纤维细胞,并在高达50℃的高温下进行损伤处理。通过细胞活力测定、细胞毒性水平、细胞增殖和促凋亡表达确定烧伤模型的最佳温度。为了评估预分化皮肤样细胞的有效性,将角质形成细胞和成纤维细胞样细胞分别与受伤的角质形成细胞和受伤的成纤维细胞共培养。结果表明,诱导角化细胞和成纤维细胞热损伤的最佳温度均为50℃。在这个温度下,两种类型的细胞(角质形成细胞和成纤维细胞)都表现出形态改变,细胞损伤严重,活力最低,促凋亡标志物表达较高,增殖基因表达较低。预分化细胞的共培养增加了细胞活力和增殖,同时减少了细胞凋亡。我们成功地建立了体外烧伤模型,这可能有助于评估细胞的创面愈合潜力。此外,预分化皮肤样细胞是治疗严重烧伤的潜在来源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pre-Differentiated Skin-Like Cells can Alleviate In Vitro Burn Injury
Considering importance of stem cell based therapies for wound healing, we have previously established protocols for successful differentiation of stem cells (isolated from placenta) into skin-like cells (keratinocytes and fibroblasts). In the current study we aim to evaluate the effect of pre-differentiated skin-like-cells on wound healing potential using an in vitro burn injury model. The amniotic epithelial cells (AECs) and umbilical cord mesenchymal stem cells (UCMSCs) obtained from amniotic membrane and umbilical cord tissue; respectively, were differentiated into skin-like cells (keratinocyte and fibroblasts respectively). In order to make an in vitro burn injury model, keratinocytes and fibroblasts were isolated from rats and insulted with high temperature (up to 50oC). The optimal temperature for burn injury models was determined using viability assay, cytotoxicity level, proliferation, and expression of pro-apoptotic. In order to assess effectiveness of pre-differentiated skin like cells, the keratinocyte- and fibroblasts-like cells were co-cultured with injured keratinocytes and injured fibroblasts, respectively. Results indicated that optimal temperature for the induction of heat injury for both keratinocytes and fibroblasts was 50oC. At this temperature both types of cells (keratinocytes and fibroblasts) showed modified morphology, drastic cellular injury, least viability, higher expression of pro-apoptotic markers and lower expression of proliferation genes. Co-culturing of pre-differentiated cells leads to an increase in viability and proliferation concurrent with decreased apoptosis. We have established successfully in vitro model of burn injury that might be helpful to evaluate the wound healing potential of cells. Further, predifferentiated skin-like cells are a potential source for the treatment of severe burn injuries.
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