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通过调节 Shh 和 Fgf8 脑前体组织中心来恢复墨西哥盲眼脂鲤胚胎的眼睛大小。

Restoring eye size in Astyanax mexicanus blind cavefish embryos through modulation of the Shh and Fgf8 forebrain organising centres.

机构信息

Equipe Développement Evolution du Cerveau Antérieur, UPR3294 NeD, CNRS, Institut Alfred Fessard, 91198 Gif-sur-Yvette, France.

出版信息

Development. 2011 Jun;138(12):2467-76. doi: 10.1242/dev.054106.

DOI:10.1242/dev.054106
PMID:21610028
Abstract

The cavefish morph of the Mexican tetra (Astyanax mexicanus) is blind at adult stage, although an eye that includes a retina and a lens develops during embryogenesis. There are, however, two major defects in cavefish eye development. One is lens apoptosis, a phenomenon that is indirectly linked to the expansion of ventral midline sonic hedgehog (Shh) expression during gastrulation and that induces eye degeneration. The other is the lack of the ventral quadrant of the retina. Here, we show that such ventralisation is not extended to the entire forebrain because fibroblast growth factor 8 (Fgf8), which is expressed in the forebrain rostral signalling centre, is activated 2 hours earlier in cavefish embryos than in their surface fish counterparts, in response to stronger Shh signalling in cavefish. We also show that neural plate patterning and morphogenesis are modified in cavefish, as assessed by Lhx2 and Lhx9 expression. Inhibition of Fgf receptor signalling in cavefish with SU5402 during gastrulation/early neurulation mimics the typical surface fish phenotype for both Shh and Lhx2/9 gene expression. Fate-mapping experiments show that posterior medial cells of the anterior neural plate, which lack Lhx2 expression in cavefish, contribute to the ventral quadrant of the retina in surface fish, whereas they contribute to the hypothalamus in cavefish. Furthermore, when Lhx2 expression is rescued in cavefish after SU5402 treatment, the ventral quadrant of the retina is also rescued. We propose that increased Shh signalling in cavefish causes earlier Fgf8 expression, a crucial heterochrony that is responsible for Lhx2 expression and retina morphogenesis defect.

摘要

墨西哥脂鲤的洞穴鱼形态在成鱼阶段是盲的,尽管在胚胎发生过程中会发育出包括视网膜和晶状体在内的眼睛。然而,洞穴鱼眼睛发育存在两个主要缺陷。一个是晶状体凋亡,这一现象与原肠胚形成过程中腹中线 sonic hedgehog (Shh) 表达的扩张间接相关,并导致眼睛退化。另一个是视网膜腹侧象限的缺失。在这里,我们表明这种腹侧化并没有扩展到整个前脑,因为在洞穴鱼胚胎中,纤维母细胞生长因子 8 (Fgf8) 比其表面鱼对应物更早被激活,这是对洞穴鱼中更强的 Shh 信号的反应,而 Fgf8 在脑前信号中心表达。我们还表明,神经板模式形成和形态发生在洞穴鱼中发生了改变,这可以通过 Lhx2 和 Lhx9 的表达来评估。在用 SU5402 在原肠胚/早期神经胚期抑制洞穴鱼的 Fgf 受体信号,会模仿 Shh 和 Lhx2/9 基因表达的典型表面鱼表型。命运图谱实验表明,在洞穴鱼中缺乏 Lhx2 表达的前神经板的后内侧细胞,在前表面鱼中有助于视网膜的腹侧象限,而在洞穴鱼中则有助于下丘脑。此外,当 SU5402 处理后在洞穴鱼中挽救 Lhx2 表达时,视网膜的腹侧象限也被挽救。我们提出,洞穴鱼中 Shh 信号的增加导致 Fgf8 表达更早,这是导致 Lhx2 表达和视网膜形态发生缺陷的关键时变。

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