Leiper Lucy J, Ou Jingxing, Walczysko Petr, Kucerova Romana, Lavery Derek N, West John D, Collinson J Martin
School of Medical Sciences, Institute of Medical Sciences, University of Aberdeen, Foresterhill, Aberdeen, United Kingdom.
Invest Ophthalmol Vis Sci. 2009 Mar;50(3):1122-8. doi: 10.1167/iovs.08-2812. Epub 2008 Nov 21.
Corneal nerves play essential roles in maintaining the ocular surface through provision of neurotrophic support, but genetic control of corneal innervation is poorly understood. The possibility of a neurotrophic failure in ocular surface disease associated with heterozygosity at the Pax6 locus (aniridia-related keratopathy [ARK]) was investigated.
Patterns of corneal innervation were studied during development and aging in mice with different Pax6 dosages and in chimeras. Immunohistochemistry and ELISA-based assays were used to determine the molecular basis of defects seen in Pax6 mutants, and wound healing assays were performed.
In adults, the Pax6(+/-) epithelium was less densely innervated than the wild-type epithelium, and radial projection of epithelial nerves was disrupted. Neurotrophic support of the corneal epithelium appeared normal. Directed nerve projection correlated with patterns of epithelial cell migration in adult wild-types, but innervation defects observed in Pax6(+/-) mice were not fully corrected in wound healing or chimeric models where directed epithelial migration was restored.
Pax6 dosage nonautonomously controls robust directed radial projection of corneal neurons, and the guidance cues for growth cone guidance are not solely dependent on directed epithelial migration. There is little evidence that ARK represents neurotrophic keratitis.
角膜神经通过提供神经营养支持在维持眼表方面发挥着重要作用,但对角膜神经支配的基因控制了解甚少。研究了与Pax6基因座杂合性相关的眼表疾病(无虹膜相关角膜病变[ARK])中神经营养功能衰竭的可能性。
研究了不同Pax6剂量的小鼠和嵌合体在发育和衰老过程中的角膜神经支配模式。采用免疫组织化学和基于酶联免疫吸附测定的方法确定Pax6突变体中所见缺陷的分子基础,并进行伤口愈合试验。
在成年小鼠中,Pax6(+/-)上皮的神经支配密度低于野生型上皮,且上皮神经的径向投射受到破坏。角膜上皮的神经营养支持似乎正常。在成年野生型小鼠中,定向神经投射与上皮细胞迁移模式相关,但在伤口愈合或恢复定向上皮迁移的嵌合模型中,Pax6(+/-)小鼠中观察到的神经支配缺陷并未完全得到纠正。
Pax6剂量非自主地控制角膜神经元强大的定向径向投射,生长锥导向的引导线索并不完全依赖于定向上皮迁移。几乎没有证据表明ARK代表神经营养性角膜炎。