Department of Ophthalmology & Visual Sciences, University of Maryland School of Medicine, Baltimore, MD, USA.
Exp Eye Res. 2012 Feb;95(1):48-53. doi: 10.1016/j.exer.2011.10.005. Epub 2011 Oct 25.
Vasoactive intestinal peptide (VIP) and ciliary neurotrophic factor (CNTF) are identified as autocrines of human corneal endothelial (CE) cells working in concert to maintain the differentiated state and promote the survival of the corneal endothelium. From VIP gene knockdown study, endogenous VIP is shown to maintain the level of the differentiation marker, the adhesion molecule N-cadherin, CE cell size, shape, and retention, in situ in the human donor corneoscleral explants. Exogenous VIP protects the corneal endothelium against the killing effect of oxidative stress, in part by upholding ATP levels in CE cells dying of oxidative stress-induced injury, allowing them to die of an apoptotic death instead of an acute necrotic one. The switch from the acute necrosis to the programmed cell death (apoptosis) may have allowed the injured CE cell to be rescued by the VIP-upregulated pathways, including those of Bcl-2 and N-cadherin, and resulted in long-term CE cell survival. The endogenous VIP in CE cells is upregulated by CNTF, which is released by CE cells surviving the oxidative stress. The CNTF receptor (CNTFRα) is expressed in CE cells in human donor corneoscleral explant and gradually becomes lost during corneal storage. VIP treatment (10(-8) M, 37 °C, 30 min) prior to storage of freshly dissected human donor corneoscleral explants increases their CE cell CNTFRα level and responsiveness to CNTF in upregulating the gap junctional protein connexin-43 expression. VIP treatment of both fresh and preserved corneoscleral explants reduces CE damage in the corneoscleral explants and in the corneal buttons trephined from them. CE cell loss is a critical risk factor in corneal graft failure at any time in the life of the graft, which can be as late as 5-10 years after an initially successful transplant. A new procedure, Descemet's stripping automated endothelial keratoplasty (DSAEK), which is superior to the traditional full thickness transplantation in many aspects, nevertheless subjects the corneal endothelium to extensive mechanical forces, resulting in even more pronounced CE cell loss than the traditional technique. Whereas it is known that cells transduce mechanical stress through N-cadherin, stimulation of the N-cadherin pathway increases the anti-apoptotic protein Bcl-2 expression. Since N-cadherin and Bcl-2 in the corneal endothelium are both upregulated by VIP, we aim to strengthen the CE sheet by VIP treatments of the corneoscleral explants for full thickness traditional corneal transplantation and pre-cut corneas for DSAEK.
血管活性肠肽 (VIP) 和睫状神经营养因子 (CNTF) 被鉴定为人类角膜内皮 (CE) 细胞的自分泌因子,共同作用以维持分化状态并促进角膜内皮的存活。从 VIP 基因敲低研究中可以看出,内源性 VIP 维持着分化标志物,即黏附分子 N-钙黏蛋白的水平,CE 细胞的大小、形状和保留,原位在人供体角膜巩膜外植体中。外源性 VIP 保护角膜内皮免受氧化应激的杀伤作用,部分通过维持 CE 细胞因氧化应激诱导损伤而死亡时的 ATP 水平,使它们死于凋亡而不是急性坏死。从急性坏死到程序性细胞死亡 (凋亡) 的转变可能使受损的 CE 细胞能够通过 VIP 上调的途径获救,包括 Bcl-2 和 N-钙黏蛋白途径,并导致 CE 细胞长期存活。CE 细胞中的内源性 VIP 被 CNTF 上调,CNTF 由存活于氧化应激下的 CE 细胞释放。CNTF 受体 (CNTFRα) 在人供体角膜巩膜外植体中的 CE 细胞中表达,并在角膜储存过程中逐渐丢失。在新鲜分离的人供体角膜巩膜外植体储存之前用 VIP(10(-8) M,37°C,30 分钟)处理可增加其 CE 细胞 CNTFRα 水平,并在通过上调间隙连接蛋白连接蛋白-43 的表达来响应 CNTF 方面提高其反应性。VIP 处理新鲜和保存的角膜巩膜外植体均可减少角膜巩膜外植体和从其中切取的角膜环中的 CE 损伤。CE 细胞丢失是角膜移植物在移植物寿命的任何时候(甚至在最初成功移植后 5-10 年)发生失败的关键危险因素。一种新的程序,Descemet 的剥离自动内皮角膜移植术(DSAEK),在许多方面优于传统的全厚度移植,但它使角膜内皮受到广泛的机械力,导致 CE 细胞丢失比传统技术更为明显。虽然已知细胞通过 N-钙黏蛋白转导机械应激,但 N-钙黏蛋白途径的刺激会增加抗凋亡蛋白 Bcl-2 的表达。由于 N-钙黏蛋白和 Bcl-2 在角膜内皮中均由 VIP 上调,因此我们旨在通过 VIP 处理角膜巩膜外植体来增强全厚度传统角膜移植术和用于 DSAEK 的预切割角膜的 CE 片。