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Chronic wound state exacerbated by oxidative stress in Pax6+/- aniridia-related keratopathy.在Pax6+/-无虹膜相关角膜病变中,氧化应激加剧慢性伤口状态。
J Pathol. 2008 Aug;215(4):421-30. doi: 10.1002/path.2371.
2
PAX6 dosage effects on corneal development, growth, and wound healing.PAX6剂量对角膜发育、生长及伤口愈合的影响。
Dev Dyn. 2008 May;237(5):1295-306. doi: 10.1002/dvdy.21528.
3
Age-related changes in rat corneal epithelial nerve density.大鼠角膜上皮神经密度的年龄相关变化。
Invest Ophthalmol Vis Sci. 2008 Mar;49(3):910-6. doi: 10.1167/iovs.07-1324.
4
Grid-free models of multicellular systems, with an application to large-scale vortices accompanying primitive streak formation.多细胞系统的无网格模型及其在原条形成伴随的大规模涡旋中的应用。
Curr Top Dev Biol. 2008;81:157-82. doi: 10.1016/S0070-2153(07)81005-2.
5
Transgenic corneal neurofluorescence in mice: a new model for in vivo investigation of nerve structure and regeneration.小鼠转基因角膜神经荧光成像:一种用于体内研究神经结构和再生的新模型。
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6
The roles of calcium signaling and ERK1/2 phosphorylation in a Pax6+/- mouse model of epithelial wound-healing delay.钙信号传导和ERK1/2磷酸化在上皮伤口愈合延迟的Pax6+/-小鼠模型中的作用。
BMC Biol. 2006 Aug 16;4:27. doi: 10.1186/1741-7007-4-27.
7
Electrical signals control wound healing through phosphatidylinositol-3-OH kinase-gamma and PTEN.电信号通过磷脂酰肌醇-3-羟基激酶-γ和PTEN控制伤口愈合。
Nature. 2006 Jul 27;442(7101):457-60. doi: 10.1038/nature04925.
8
Mapping the corneal sub-basal nerve plexus in keratoconus by in vivo laser scanning confocal microscopy.通过活体激光扫描共聚焦显微镜绘制圆锥角膜中的角膜基底膜下神经丛。
Invest Ophthalmol Vis Sci. 2006 Apr;47(4):1348-51. doi: 10.1167/iovs.05-1217.
9
Mapping of the normal human corneal sub-Basal nerve plexus by in vivo laser scanning confocal microscopy.利用活体激光扫描共聚焦显微镜对正常人角膜基底膜下神经丛进行成像
Invest Ophthalmol Vis Sci. 2005 Dec;46(12):4485-8. doi: 10.1167/iovs.05-0794.
10
Controlling cell behavior electrically: current views and future potential.通过电方式控制细胞行为:当前观点与未来潜力
Physiol Rev. 2005 Jul;85(3):943-78. doi: 10.1152/physrev.00020.2004.

Pax6对角膜神经支配模式的调控。

Control of patterns of corneal innervation by Pax6.

作者信息

Leiper Lucy J, Ou Jingxing, Walczysko Petr, Kucerova Romana, Lavery Derek N, West John D, Collinson J Martin

机构信息

School of Medical Sciences, Institute of Medical Sciences, University of Aberdeen, Foresterhill, Aberdeen, United Kingdom.

出版信息

Invest Ophthalmol Vis Sci. 2009 Mar;50(3):1122-8. doi: 10.1167/iovs.08-2812. Epub 2008 Nov 21.

DOI:10.1167/iovs.08-2812
PMID:19029029
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2654056/
Abstract

PURPOSE

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

目的

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。

方法

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。

结果

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。

结论

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。