Department of Clinical Laboratory Science, Graduate School of Medical Science, Kanazawa University, 5-11-80 Kodatsuno, Kanazawa 920-0942, Japan.
AI Hospital/Macro Signal Dynamics Research and Development Center, 5-11-80 Kodatsuno, Kanazawa 920-0942, Japan.
Int J Mol Sci. 2023 Feb 7;24(4):3253. doi: 10.3390/ijms24043253.
In contrast to the case in mammals, the fish optic nerve can spontaneously regenerate and visual function can be fully restored 3-4 months after optic nerve injury (ONI). However, the regenerative mechanism behind this has remained unknown. This long process is reminiscent of the normal development of the visual system from immature neural cells to mature neurons. Here, we focused on the expression of three Yamanaka factors (Oct4, Sox2, and Klf4: OSK), which are well-known inducers of induced pluripotent stem (iPS) cells in the zebrafish retina after ONI. mRNA expression of OSK was rapidly induced in the retinal ganglion cells (RGCs) 1-3 h after ONI. Heat shock factor 1 (HSF1) mRNA was most rapidly induced in the RGCs at 0.5 h. The activation of OSK mRNA was completely suppressed by the intraocular injection of HSF1 morpholino prior to ONI. Furthermore, the chromatin immunoprecipitation assay showed the enrichment of OSK genomic DNA bound to HSF1. The present study clearly showed that the rapid activation of Yamanaka factors in the zebrafish retina was regulated by HSF1, and this sequential activation of HSF1 and OSK might provide a key to unlocking the regenerative mechanism of injured RGCs in fish.
与哺乳动物的情况相反,鱼类视神经可以自发再生,视神经损伤 (ONI) 后 3-4 个月即可完全恢复视觉功能。然而,这背后的再生机制仍然未知。这个漫长的过程让人想起了视觉系统从未成熟的神经细胞到成熟神经元的正常发育过程。在这里,我们专注于在 ONI 后斑马鱼视网膜中三种 Yamanaka 因子 (Oct4、Sox2 和 Klf4:OSK) 的表达,这三种因子是诱导多能干细胞 (iPS) 的众所周知的诱导物。OSK 的 mRNA 表达在 ONI 后 1-3 小时内迅速诱导视网膜神经节细胞 (RGC)。在 RGC 中,热休克因子 1 (HSF1) 的 mRNA 最快在 0.5 小时内诱导。在 ONI 之前,通过眼内注射 HSF1 嵌合体完全抑制了 OSK mRNA 的激活。此外,染色质免疫沉淀分析表明,与 HSF1 结合的 OSK 基因组 DNA 丰富。本研究清楚地表明,HSF1 调节了斑马鱼视网膜中 Yamanaka 因子的快速激活,HSF1 和 OSK 的这种顺序激活可能为揭示鱼类受损 RGC 再生机制提供了关键。