Takatsuka Kenji, Hatakeyama Jun, Bessho Yasumasa, Kageyama Ryoichiro
Institute for Virus Research, Kyoto University, Shogoin-Kawahara, Sakyo, Kyoto 606-8507, Japan.
Brain Res. 2004 Apr 9;1004(1-2):148-55. doi: 10.1016/j.brainres.2004.01.045.
During retinal development, common precursors give rise to various types of cells in a time course specific to each cell type. Previously, we demonstrated that the bHLH gene Hes1 inhibits neuronal differentiation whereas, in Hes1-null retina, precursors prematurely differentiate into neurons and form abnormal rosette-like structures. Thus, Hes1 is essential for maintenance of precursors and morphogenesis of the neural retina. However, the precise causal link between premature differentiation and abnormal structures remains to be determined. Here, we found that misexpression of Hes1 in the developing retina promotes formation of undifferentiated precursor-like cells, whereas in Hes1-null retina, precursors are not properly maintained and prematurely differentiate into ganglion cells. Strikingly, those prematurely differentiated ganglion cells erupt into the subretinal space through the regions where precursors and the outer limiting membrane are lost. These results indicate that Hes1 maintains precursors and the outer limiting membrane and thereby regulates retinal morphogenesis.
在视网膜发育过程中,常见的前体细胞会在特定于每种细胞类型的时间进程中分化为各种类型的细胞。此前,我们证明bHLH基因Hes1抑制神经元分化,而在Hes1基因缺失的视网膜中,前体细胞会过早分化为神经元并形成异常的玫瑰花结样结构。因此,Hes1对于维持前体细胞和神经视网膜的形态发生至关重要。然而,过早分化与异常结构之间的确切因果关系仍有待确定。在这里,我们发现,在发育中的视网膜中过表达Hes1会促进未分化的前体细胞样细胞的形成,而在Hes1基因缺失的视网膜中,前体细胞无法得到正常维持并过早分化为神经节细胞。引人注目的是,那些过早分化的神经节细胞会通过前体细胞和外界膜缺失的区域突入视网膜下间隙。这些结果表明,Hes1维持前体细胞和外界膜,从而调节视网膜的形态发生。