CUO-Recherche, Médecine Régénératrice, Centre de recherche du CHU de Québec and Centre de Recherche en Organogénèse expérimentale de l'Université Laval/LOEX, Université Laval, Québec, QC, Canada.
Département d'Ophtalmologie, Faculté de médecine, Université Laval, Québec, QC, Canada.
J Tissue Eng Regen Med. 2019 Sep;13(9):1595-1608. doi: 10.1002/term.2912. Epub 2019 Jul 18.
Damage to the corneal epithelium triggers important changes in the extracellular matrix (ECM) to which basal human corneal epithelial cells (hCECs) attach. These changes are perceived by integrin receptors that activate different intracellular signalling pathways, ultimately leading to re-epithelialization of the injured epithelium. In this study, we investigated the impact of pharmacological inhibition of specific signal transduction mediators on corneal wound healing using both monolayers of hCECs and the human tissue-engineered cornea (hTEC) as an in vitro 3D model. RNA and proteins were isolated from the wounded and unwounded hTECs to conduct gene profiling analyses and protein kinase arrays. The impact of WNK1 inhibition was evaluated on the wounded hTECs as well as on hCECs monolayers using a scratch wound assay. Gene profiling and protein kinase arrays revealed that expression and activity of several mediators from the integrin-dependent signaling pathways were altered in response to the ECM changes occurring during corneal wound healing. Phosphorylation of the WNK1 kinase turned out to be the most striking activation event going on during this process. The inhibition of WNK1 by WNK463 reduced the rate of corneal wound closure in both the hTEC and hCECs grown in monolayer compared with their respective negative controls. WNK463 also reduced phosphorylation of the WNK1 downstream targets SPAK/OSR1 in wounded hTECs. These in vitro results allowed for a better understanding of the cellular and molecular mechanisms involved in corneal wound healing and identified WNK1 as a kinase important to ensure proper wound healing of the cornea.
角膜上皮细胞损伤会引发细胞外基质(ECM)的重要变化,基底人角膜上皮细胞(hCECs)附着在 ECM 上。这些变化被整合素受体感知,激活不同的细胞内信号通路,最终导致受损上皮的再上皮化。在这项研究中,我们使用单层 hCECs 和人组织工程角膜(hTEC)作为体外 3D 模型,研究了特定信号转导介质的药理学抑制对角膜伤口愈合的影响。从受伤和未受伤的 hTEC 中分离 RNA 和蛋白质,进行基因谱分析和蛋白激酶阵列分析。使用划痕实验评估 WNK1 抑制对受伤的 hTEC 以及单层 hCECs 的影响。基因谱和蛋白激酶阵列分析显示,整合素依赖的信号通路中的几种介质的表达和活性在角膜伤口愈合过程中发生的 ECM 变化的刺激下发生改变。WNK1 激酶的磷酸化是该过程中最显著的激活事件。与各自的阴性对照相比,WNK463 通过抑制 WNK1 降低了 hTEC 和在单层中培养的 hCECs 的角膜伤口闭合率。WNK463 还降低了受伤的 hTEC 中 WNK1 下游靶标 SPAK/OSR1 的磷酸化。这些体外结果有助于更好地理解角膜伤口愈合中涉及的细胞和分子机制,并确定 WNK1 是确保角膜伤口正常愈合的重要激酶。