Moore Kathryn B, Mood Kathleen, Daar Ira O, Moody Sally A
Department of Anatomy and Cell Biology, The George Washington University Medical Center, Washington, DC 20037, USA.
Dev Cell. 2004 Jan;6(1):55-67. doi: 10.1016/s1534-5807(03)00395-2.
The definitive retinal progenitors of the eye field are specified by transcription factors that both promote a retinal fate and control cell movements that are critical for eye field formation. However, the molecular signaling pathways that regulate these movements are largely undefined. We demonstrate that both the FGF and ephrin pathways impact eye field formation. Activating the FGF pathway before gastrulation represses cellular movements in the presumptive anterior neural plate and prevents cells from expressing a retinal fate, independent of mesoderm induction or anterior-posterior patterning. Inhibiting the FGF pathway promotes cell dispersal and significantly increases eye field contribution. ephrinB1 reverse signaling is required to promote cellular movements into the eye field, and can rescue the FGF receptor-induced repression of retinal fate. These results indicate that FGF modulation of ephrin signaling regulates the positioning of retinal progenitor cells within the definitive eye field.
眼区的确定性视网膜祖细胞由转录因子指定,这些转录因子既促进视网膜命运,又控制对眼区形成至关重要的细胞运动。然而,调节这些运动的分子信号通路在很大程度上尚未明确。我们证明,FGF和ephrin信号通路均影响眼区形成。在原肠胚形成之前激活FGF信号通路会抑制假定前神经板中的细胞运动,并阻止细胞表达视网膜命运,这与中胚层诱导或前后模式无关。抑制FGF信号通路会促进细胞分散,并显著增加眼区的贡献。ephrinB1反向信号传导是促进细胞移入眼区所必需的,并且可以挽救FGF受体诱导的视网膜命运抑制。这些结果表明FGF对ephrin信号的调节作用调节了确定性眼区内视网膜祖细胞的定位。