Department of Human Anatomy, Histology and Embryology, Qingdao University, Qingdao, China.
Department of Human Anatomy, Histology and Embryology, Qingdao University, Qingdao, China; Institute of Stem Cell Regeneration Medicine, School of Basic Medicine, Qingdao University, Qingdao, China.
Am J Pathol. 2021 Nov;191(11):1974-1985. doi: 10.1016/j.ajpath.2021.07.010. Epub 2021 Aug 12.
Aquaporins (AQPs) are a highly conserved group of membrane proteins that play critical roles in water and small solute transport across epithelial and endothelial barriers. The aim of this study was to determine whether AQP5, a well-known water channel protein, also plays a role in corneal epithelial wound healing. AQP5 knockout (AQP5) mice were generated using CRISPR/Cas9. A corneal wound healing model was established using epithelial debridement of corneas. The time to corneal epithelial and nerve regeneration was significantly delayed in the AQP5 mice. Reduction in Ki-67-positive cells and nerve growth factor (NGF) expression was confirmed in the AQP5 mice during healing. Epithelial and nerve regeneration rates were significantly increased in the AQP5 mice after treatment with NGF, which was accompanied by recovered levels of phosphorylated Akt. NGF treatment also improved the recovery of corneal nerve fiber density and sensitivity in the AQP5 mice. While the promotion of NGF induced corneal epithelial and nerve regeneration, Akt inhibitor reversed Akt reactivation. A significant impairment of corneal wound healing in the AQP5 mice resulted from distinct defects in corneal epithelial cell proliferation and nerve regeneration. These results provide evidence for the involvement of aquaporin in cell proliferation and suggest that AQP5 induction could be a potential therapy for accelerating the resurfacing of corneal defects.
水通道蛋白(AQP)是一组高度保守的膜蛋白,在跨上皮和内皮屏障的水和小分子转运中发挥关键作用。本研究旨在确定水通道蛋白 5(AQP5),一种众所周知的水通道蛋白,是否也在角膜上皮伤口愈合中发挥作用。使用 CRISPR/Cas9 生成 AQP5 敲除(AQP5)小鼠。使用角膜上皮清创术建立角膜伤口愈合模型。AQP5 小鼠的角膜上皮和神经再生时间明显延迟。在愈合过程中,AQP5 小鼠中 Ki-67 阳性细胞和神经生长因子(NGF)表达减少得到证实。AQP5 小鼠经 NGF 治疗后,上皮和神经再生率显著增加,同时 Akt 的磷酸化水平也得到恢复。NGF 治疗还改善了 AQP5 小鼠角膜神经纤维密度和敏感性的恢复。虽然 NGF 的促进作用诱导了角膜上皮和神经的再生,但 Akt 抑制剂逆转了 Akt 的再激活。AQP5 小鼠角膜伤口愈合明显受损,这是由于角膜上皮细胞增殖和神经再生的明显缺陷所致。这些结果为水通道蛋白参与细胞增殖提供了证据,并表明 AQP5 的诱导可能是加速角膜缺陷修复的一种潜在治疗方法。