Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden.
Department of Hand Surgery, Plastic Surgery and Burns, Department of Biomedical and Clinical Sciences, Linköping University Hospital, Linköping, Sweden.
Exp Dermatol. 2022 May;31(5):764-774. doi: 10.1111/exd.14515. Epub 2022 Jan 15.
Cutaneous wounds can lead to huge suffering for patients. Early fetal wounds have the capacity to regenerate without scar formation. Amniotic fluid (AF), containing hyaluronic acid (HA), may contribute to this regenerative environment. We aimed to analyse changes in gene expression when human keratinocytes are exposed to AF or HA. Human keratinocytes were cultured to subconfluence, starved for 12 h and then randomised to be maintained in (1) Dulbecco's modified Eagle's medium (DMEM), (2) DMEM with 50% AF, or (3) DMEM with 50% fetal calf serum (FCS). Transcriptional changes were analysed using microarray and enriched with WebGestalt and Enrichr. Additionally, eight diagnostic genes were analysed using semiquantitative real-time PCR to investigate epidermal differentiation and cellular stress after HA exposure as an alternative for AF exposure. The AF and FCS treatments resulted in enrichment of genes relating to varied aspects of epidermal and keratinocyte biology. In particular, p63-, AP1- and NFE2L2- (Nrf2) associated genes were found significantly regulated in both treatments. More genes regulated by FCS treatment were associated with inflammatory signalling, whilst AF treatment was dominantly associated with molecular establishment of epidermis and lipid metabolic activity. HA exposure mostly resulted in gene regulation that was congruent with the AF microarray group, with increased expression of ITGA6 and LOR. We conclude that AF exposure enhances keratinocyte differentiation in vitro, which suggests that AF constituents can be beneficial for wound-healing applications.
皮肤创伤会给患者带来巨大的痛苦。早期胎儿伤口具有无瘢痕形成的再生能力。含有透明质酸(HA)的羊水(AF)可能有助于这种再生环境。我们旨在分析人类角质形成细胞暴露于 AF 或 HA 时基因表达的变化。将人类角质形成细胞培养至亚汇合状态,饥饿 12 小时,然后随机分为以下三组:(1)DMEM,(2)含 50% AF 的 DMEM,或(3)含 50%胎牛血清(FCS)的 DMEM。使用微阵列分析转录变化,并使用 WebGestalt 和 Enrichr 进行富集。此外,使用半定量实时 PCR 分析八个诊断基因,以研究 HA 暴露后表皮分化和细胞应激,作为 AF 暴露的替代方法。AF 和 FCS 处理导致与表皮和角质形成细胞生物学各个方面相关的基因富集。特别是,在两种处理中均发现 p63、AP1 和 NFE2L2(Nrf2)相关基因的表达显著调节。FCS 处理调节的更多基因与炎症信号转导有关,而 AF 处理主要与表皮的分子建立和脂质代谢活性有关。HA 暴露主要导致与 AF 微阵列组一致的基因调控,ITGA6 和 LOR 的表达增加。我们得出结论,AF 暴露增强了体外角质形成细胞的分化,这表明 AF 成分可能有益于伤口愈合应用。