New study suggests that aquaporin could be key to repairing corneal defects

角膜缺陷通常愈合本身,而是认真的injuries that are left untreated can result in inflammation, infection, ulceration and even blindness. A new study provides exciting evidence supporting the involvement of aquaporins in corneal cell proliferation and nerve regeneration and suggests aquaporin 5 (AQP5) induction as a potential therapy to accelerate the resurfacing of corneal defects, report scientists inThe American Journal of Pathology.

The cornea, which consists of transparent tissue in the outermost layer of the eye, acts as a barrier against external stimuli. It also plays a key role in vision.

"As a member of aquaporin family, AQP5 is expressed in cornea, which is related to many eye diseases," explained lead investigator Peng Chen, Ph.D., Department of Human Anatomy, Histology and Embryology, School of Basic Medicine, Qingdao University, Shandong Province; and Institute of Stem Cell Regeneration Medicine, School of Basic Medicine, Qingdao University, Qingdao, China. "If a corneal injury cannot heal in time, it may lead to pathogen invasion and result in corneal inflammation, turbidity, ulcer and even blindness. In previous studies, we found that AQP5 deficiency can cause corneal epithelial punctate defects. There is also increasing evidence that nerve growth factor (NGF) plays a key role in corneal wound healing. AQP5 deficiency can slow down the repair of corneal epithelial injury in mice, but its specific mechanism remained unclear. We hypothesized that AQP5 plays an important role in one or more stages of corneal epithelialregenerationand explored the specific mechanism of AQP5."

Investigators generated anAqp5knockout (Aqp5^-/-)mouse modeland performed corneal wound healing on corneas from whichepithelial cellshad been scraped away. They used 75 maleAqp5^+/+mice and 189 maleAqp5^-/-mice aged 10 to 12 weeks. Time to corneal epithelial and nerve regeneration was significantly delayed in theAqp5^-/-mice. To determine the role of NGF in the repair of corneal epithelial injury, NGF was injected in the subconjunctival space after corneal epithelium was scraped off inAqp5^-/-mice. The epithelial and nerve regeneration rate were significantly promoted inAqp5^-/-mice with the treatment of NGF, which also improved the recovery of corneal nerve fiber density and sensitivity inAqp5^-/-mice, accompanied by recovered levels of phosphorylated Akt.

The investigators also administered an Akt inhibitor in addition to NGF inAqp5^-/-mice to determine the mechanism of NGF regulating the repair rate of corneal epithelial injury. However, the promotion of NGF induced corneal epithelial and nerve regeneration rate and Akt reactivation was reversed by the Akt inhibitor.

"It is exciting to find that Aqp5 deficiency can affect thenerveregeneration ofmiceby affecting the activation of NGF and Akt signaling pathways, which is not found in previous studies," commented Dr. Chen. "These results need to be confirmed in aclinical setting, but they provide evidence for the involvement of aquaporins in cell proliferation andnerve regenerationand suggest AQP5 induction as a possible therapy to accelerate the resurfacing of corneal defects."

Aquaporins (AQPs), also called water channels, are channel proteins that form pores in the membrane of biological cells, mainly facilitating transport of water betweencellsand are expressed in the corneal epithelium. Thirteen different types of AQPs have been detected in mammals. As transmembrane proteins, they play a significant role in maintaining cell water homeostasis.