Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Beijing Key Laboratory of Reproductive Endocrinology and Assisted Reproductive Technology, Key Laboratory of Assisted Reproduction, Ministry of Education, Peking University Third Hospital, Beijing, 100191, China.
Department of Ophthalmology, Beijing Key Laboratory of Restoration of Damaged Ocular Nerve, Peking University Third Hospital, Beijing, 100191, China; Department of Ophthalmology, West China Hospital, Sichuan University, Chengdu, 610041, China.
Exp Eye Res. 2021 Aug;209:108629. doi: 10.1016/j.exer.2021.108629. Epub 2021 May 23.
The shortage of human donor corneas has raised important concerns about engineering of corneal endothelial cells (CECs) for clinical use. However, due to the limited proliferative capacity of human CECs, driving them into proliferation and regeneration may be difficult. Unlike human CECs, rabbit CECs have a marked proliferative capacity. To clarify the potential reason for this difference, we analysed the proteomes of four human corneal endothelium samples and four rabbit corneal endothelium samples with quantitative label-free proteomics and downstream analysis. We discovered that vitamin and selenocompound metabolism and some signaling pathways such as NF-kappa B signaling pathway differed between the samples. Moreover, TGFβ, PITX2 and keratocan were distinctively expressed in rabbit samples, which might be associated with active proliferation in rabbit CECs. This study illustrates the proteomic differences between human and rabbit CECs and might promote CEC engineering strategies.
人供体角膜的短缺引发了人们对用于临床的角膜内皮细胞(CEC)工程的高度关注。然而,由于人 CEC 的增殖能力有限,促使它们增殖和再生可能较为困难。与人类 CEC 不同,兔 CEC 具有明显的增殖能力。为了阐明这种差异的潜在原因,我们采用定量无标记蛋白质组学和下游分析方法,分析了四个人类角膜内皮样本和四个兔角膜内皮样本的蛋白质组。我们发现,维生素和硒化合物代谢以及 NF-κB 信号通路等一些信号通路在样本之间存在差异。此外,兔样本中 TGFβ、PITX2 和角膜蛋白聚糖的表达明显不同,这可能与兔 CEC 的活跃增殖有关。本研究阐明了人 CEC 和兔 CEC 之间的蛋白质组差异,并可能促进 CEC 工程策略的发展。