Department of Biomedical Engineering, Tufts University, 4 Colby Street, Medford, MA, 02155, USA.
Center for Translational Ocular Immunology and Cornea Service, Department of Ophthalmology, Tufts Medical Center, Tufts University School of Medicine, Boston, MA, USA.
Prog Retin Eye Res. 2019 Jul;71:88-113. doi: 10.1016/j.preteyeres.2018.11.005. Epub 2018 Nov 16.
The cornea is a valuable tissue for studying peripheral sensory nerve structure and regeneration due to its avascularity, transparency, and dense innervation. Somatosensory innervation of the cornea serves to identify changes in environmental stimuli at the ocular surface, thereby promoting barrier function to protect the eye against injury or infection. Due to regulatory demands to screen ocular safety of potential chemical exposure, a need remains to develop functional human tissue models to predict ocular damage and pain using in vitro-based systems to increase throughput and minimize animal use. In this review, we summarize the anatomical and functional roles of corneal innervation in propagation of sensory input, corneal neuropathies associated with pain, and the status of current in vivo and in vitro models. Emphasis is placed on tissue engineering approaches to study the human corneal pain response in vitro with integration of proper cell types, controlled microenvironment, and high-throughput readouts to predict pain induction. Further developments in this field will aid in defining molecular signatures to distinguish acute and chronic pain triggers based on the immune response and epithelial, stromal, and neuronal interactions that occur at the ocular surface that lead to functional outcomes in the brain depending on severity and persistence of the stimulus.
角膜因其无血管、透明和密集的神经支配而成为研究周围感觉神经结构和再生的有价值组织。角膜的躯体感觉神经支配有助于识别眼表面环境刺激的变化,从而促进屏障功能,以防止眼睛受伤或感染。由于监管要求筛选潜在化学暴露的眼部安全性,因此仍然需要开发功能性人体组织模型,以使用基于体外的系统来增加吞吐量并最小化动物使用,从而预测眼部损伤和疼痛。在这篇综述中,我们总结了角膜神经支配在感觉传入传播、与疼痛相关的角膜神经病变以及当前体内和体外模型的状况中的解剖学和功能作用。重点介绍了组织工程方法,用于通过整合适当的细胞类型、控制微环境和高通量读出,在体外研究人类角膜疼痛反应,以预测疼痛诱导。该领域的进一步发展将有助于根据发生在眼表面的免疫反应以及上皮、基质和神经元相互作用来定义区分急性和慢性疼痛触发的分子特征,这些相互作用会导致大脑的功能结果,具体取决于刺激的严重程度和持续时间。