Ohta Kunimasa, Ito Ayako, Tanaka Hideaki
Department of Developmental Neurobiology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto 860-8556, Japan.
Dev Growth Differ. 2008 May;50(4):253-9. doi: 10.1111/j.1440-169X.2008.01006.x. Epub 2008 Mar 10.
We acquire information from the outside world through our eyes which contain the retina, the photosensitive component of the central nervous system. Once the adult mammalian retina is damaged, the retinal neuronal death causes a severe loss of visual function. It has been believed that the adult mammalian retina had no regenerative capacity. However, the identification of neuronal progenitor cells in the retina sheds some light on cellular therapies for damaged retinal regeneration. In this review, we highlight three potential stem/progenitor cells in the eye, the ciliary body epithelium cells, the iris pigmented epithelium cells, and Müller glia. In order to make them prime candidates for the possible treatment of retinal diseases, it is important to understand their basic characters. In addition, we discuss the key signaling molecules that function extracellularly and determine whether neuronal progenitors remain quiescent, proliferate, or differentiate. Finally, we introduce a secreted protein, Tsukushi, which is a possible candidate as a niche molecule for retinal stem/progenitor cells.
我们通过眼睛从外界获取信息,眼睛包含视网膜,它是中枢神经系统的感光组件。成年哺乳动物的视网膜一旦受损,视网膜神经元死亡会导致严重的视觉功能丧失。人们一直认为成年哺乳动物的视网膜没有再生能力。然而,视网膜中神经元祖细胞的发现为受损视网膜再生的细胞疗法带来了曙光。在这篇综述中,我们重点介绍了眼睛中的三种潜在干细胞/祖细胞,即睫状体上皮细胞、虹膜色素上皮细胞和穆勒胶质细胞。为了使它们成为治疗视网膜疾病的理想候选细胞,了解它们的基本特性很重要。此外,我们讨论了在细胞外发挥作用并决定神经元祖细胞是保持静止、增殖还是分化的关键信号分子。最后,我们介绍一种分泌蛋白——筑丝蛋白,它可能是视网膜干细胞/祖细胞的一种龛位分子候选物。