Gao Lixiong, Jin Ni, Ye Zi, Ma Tianju, Huang Yang, Li Hongyu, Du Jinlin, Li Zhaohui
Senior Department of Ophthalmology, The Third Medical Center of Chinese PLA General Hospital, Beijing, China.
Department of Endocrinology, The Second Medical Center and National Clinical Research Center for Geriatric Diseases, The Chinese PLA General Hospital, Beijing, China.
Front Cell Dev Biol. 2022 Sep 21;10:820949. doi: 10.3389/fcell.2022.820949. eCollection 2022.
The lens is a relatively special and simple organ. It has become an ideal model to study the common developmental characteristics among different organic systems. Lens development is a complex process influenced by numerous factors, including signals from the intracellular and extracellular environment. Reactive oxygen species (ROS) are a group of highly reactive and oxygen-containing molecules that can cause endoplasmic reticulum stress in lens cells. As an adaptive response to ER stress, lens cells initiate the unfolded protein response (UPR) to maintain normal protein synthesis by selectively increasing/decreasing protein synthesis and increasing the degradation of misfolded proteins. Generally, the UPR signaling pathways have been well characterized in the context of many pathological conditions. However, recent studies have also confirmed that all three UPR signaling pathways participate in a variety of developmental processes, including those of the lens. In this review, we first briefly summarize the three stages of lens development and present the basic profiles of ROS and the UPR. We then discuss the interconnections between lens development and these two mechanisms. Additionally, the potential adoption of human pluripotent stem-cell-based lentoids in lens development research is proposed to provide a novel perspective on future developmental studies.
晶状体是一个相对特殊且简单的器官。它已成为研究不同有机系统共同发育特征的理想模型。晶状体发育是一个受众多因素影响的复杂过程,这些因素包括来自细胞内和细胞外环境的信号。活性氧(ROS)是一组具有高反应性的含氧化合物分子,可在晶状体细胞中引发内质网应激。作为对内质网应激的适应性反应,晶状体细胞启动未折叠蛋白反应(UPR),通过选择性地增加/减少蛋白质合成以及增加错误折叠蛋白的降解来维持正常的蛋白质合成。一般来说,在许多病理状况下,未折叠蛋白反应信号通路已得到充分研究。然而,最近的研究也证实,所有三条未折叠蛋白反应信号通路都参与了包括晶状体发育在内的多种发育过程。在这篇综述中,我们首先简要总结晶状体发育的三个阶段,并介绍活性氧和未折叠蛋白反应的基本概况。然后我们讨论晶状体发育与这两种机制之间的相互联系。此外,还提出了在晶状体发育研究中采用基于人类多能干细胞的类晶状体,为未来的发育研究提供新的视角。