Canto-Soler M Valeria, Adler Ruben
The Department of Ophthalmology, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
Dev Biol. 2006 Jun 1;294(1):119-32. doi: 10.1016/j.ydbio.2006.02.033. Epub 2006 Mar 27.
Pax6 mutations cause complex ocular malformations, but it is uncertain whether early eye development normally requires Pax6 function in both the optic vesicle (OV) and the lens epithelium, or only in the latter. To investigate this question, we electroporated the OV with anti-Pax6 or control morpholinos before the onset of lens placode formation. Pax6 downregulation was already detectable in the OV 10 h after anti-Pax6 treatment, and was accompanied by a significant increase in the death of OV cells. A small eye-like phenotype developed thereafter, whose severity was developmental stage-dependent. When treatment was applied at Hamburger Hamilton (HH) stage 10, there was no optic cup formation, and lens development was abortive despite normal Pax6 expression in the lens epithelium. Treatment at HH stage 11 resulted in structurally normal lens and optic cup, although the latter showed abnormal expression domains for several transcription factors. Early eye development therefore requires cell-autonomous Pax6 function not only in the lens but also in the optic vesicle, where it plays a hitherto unknown role in cell survival. The results, moreover, indicate that there is a critical stage during which Pax6 expression in the OV is necessary for normal lens development.
Pax6 突变会导致复杂的眼部畸形,但目前尚不确定早期眼睛发育正常情况下是需要视泡(OV)和晶状体上皮中都有 Pax6 功能,还是仅需要后者有该功能。为了研究这个问题,我们在晶状体板形成之前,用抗 Pax6 或对照吗啉代寡核苷酸对视泡进行电穿孔。抗 Pax6 处理后 10 小时,视泡中就已检测到 Pax6 下调,同时视泡细胞死亡显著增加。此后出现了小眼样表型,其严重程度取决于发育阶段。在汉伯格 - 汉密尔顿(HH)第 10 阶段进行处理时,没有形成视杯,尽管晶状体上皮中 Pax6 表达正常,但晶状体发育失败。在 HH 第 11 阶段进行处理,晶状体和视杯结构正常,不过视杯显示出几种转录因子的表达域异常。因此,早期眼睛发育不仅在晶状体中,而且在视泡中都需要细胞自主的 Pax6 功能,Pax6 在视泡的细胞存活中发挥着迄今未知的作用。此外,结果表明存在一个关键阶段,在此期间视泡中 Pax6 的表达对于正常晶状体发育是必需的。