Department of Opthalmology, University of Rostock, Doberaner Strasse 140, 18057 Rostock, Germany.
Institute of Anatomy, University of Rostock, Gertrudenstrasse 9, 18057 Rostock, Germany.
Exp Eye Res. 2014 Aug;125:53-61. doi: 10.1016/j.exer.2014.05.006. Epub 2014 May 28.
Impaired corneal innervation and sensitivity are the main causes of corneal neurotrophic keratopathy which simultaneously also leads to poor epithelial wound healing. Restoration of the diminished communication between the corneal epithelium and trigeminal nerve is indispensable for the proper functioning of the epithelium. The present study aims to investigate corneal epithelial and trigeminal neuron interactions to shed light on corneal wound healing during neurotrophic keratopathy. Mouse trigeminal neurons and corneal epithelial cells were cultured according to standard methods. To study the effect of corneal epithelial cells on trigeminal neurons as well as the effect of trigeminal neurons on corneal epithelial cells during wound healing, conditioned media from the cultures of pure trigeminal neurons (CNM) and corneal epithelial cells (CEM) were collected freshly and applied on the other cell type. Neurite outgrowth assay and RT-PCR analysis using primers specific for substance P (SP), Map1a, Map1b were performed on trigeminal neurons in the presence of CEM. We observed an increase in the neurite outgrowth in the presence of CEM and also in co-culture with corneal epithelial cells. Increase in the expression of SP mRNA and a decrease in the expression of Map1b mRNA was observed in the presence of CEM. We also observed the presence of epithelial-to-mesenchymal transition (EMT)-like phenomenon during wound healing using a scratch assay in primary corneal epithelial cultures. This system was further employed to study the effect of CNM on corneal epithelial cells in the context of wound healing to find the effect of trigeminal neurons on epithelial cells. RT-PCR analysis of Pax6 expression in corneal epithelial cell cultures with scratch served as a positive control. Further, we also show the expression of bone morphogenetic protein 7 (BMP7) mRNA in corneal epithelial cells which is decreased gradually along with Pax6 mRNA when cultured together in the presence of CNM. The expression and down regulation of BMP7 in the presence of CNM was further confirmed at the protein level by western blotting. From this study it seems that the epithelial and neuronal interactions in the cornea may contribute to the corneal innervation as well as recovery of corneal epithelial cells during injury. Appraising the differences in the expression of various signalling molecules during EMT of epithelial cells in the presence of SP and BMP7 gives an insight into the detailed dissection of the involved signalling pathways to develop future therapeutics.
角膜神经支配和敏感性的损伤是角膜神经营养性角膜病变的主要原因,同时也导致上皮愈合不良。恢复角膜上皮与三叉神经之间减弱的通讯对于上皮的正常功能是必不可少的。本研究旨在探讨角膜上皮和三叉神经神经元之间的相互作用,以阐明神经营养性角膜病变过程中的角膜伤口愈合。根据标准方法培养小鼠三叉神经神经元和角膜上皮细胞。为了研究角膜上皮细胞对三叉神经神经元的影响以及在伤口愈合过程中三叉神经神经元对角膜上皮细胞的影响,新鲜收集纯三叉神经神经元(CNM)和角膜上皮细胞(CEM)培养物的条件培养基,并将其施加于另一种细胞类型。在 CEM 存在的情况下,对三叉神经神经元进行神经突生长测定和使用特定于 P 物质(SP)、Map1a、Map1b 的引物进行 RT-PCR 分析。我们观察到在 CEM 存在下神经突生长增加,并且在与角膜上皮细胞共培养时也增加。在 CEM 存在下观察到 SP mRNA 的表达增加和 Map1b mRNA 的表达减少。我们还在用划痕实验在原代角膜上皮培养物中观察到伤口愈合过程中上皮-间充质转化(EMT)样现象。在伤口愈合的背景下,进一步使用此系统研究 CNM 对角膜上皮细胞的影响,以发现三叉神经神经元对上皮细胞的影响。划痕培养物中 Pax6 表达的 RT-PCR 分析作为阳性对照。此外,我们还显示了在 CNM 存在下角膜上皮细胞中骨形态发生蛋白 7(BMP7)mRNA 的表达,当与 Pax6 mRNA 一起培养时,其表达逐渐减少。在 CNM 存在下,通过 Western blot 进一步证实了 BMP7 的表达和下调。从这项研究中似乎可以看出,角膜中的上皮和神经元相互作用可能有助于角膜神经支配以及受伤时角膜上皮细胞的恢复。评估 SP 和 BMP7 存在时上皮细胞 EMT 过程中各种信号分子表达的差异,深入剖析涉及的信号通路,为未来的治疗方法开发提供了思路。