da Silva Susana, Cepko Constance L
Departments of Genetics and Ophthalmology, Howard Hughes Medical Institute, Harvard Medical School, Boston, MA 02115, USA.
Departments of Genetics and Ophthalmology, Howard Hughes Medical Institute, Harvard Medical School, Boston, MA 02115, USA.
Dev Cell. 2017 Jul 10;42(1):68-81.e6. doi: 10.1016/j.devcel.2017.05.024. Epub 2017 Jun 22.
Species that are highly reliant on their visual system have a specialized retinal area subserving high-acuity vision, e.g., the fovea in humans. Although of critical importance for our daily activities, little is known about the mechanisms driving the development of retinal high-acuity areas (HAAs). Using the chick as a model, we found a precise and dynamic expression pattern of fibroblast growth factor 8 (Fgf8) in the HAA anlage, which was regulated by enzymes that degrade retinoic acid (RA). Transient manipulation of RA signaling, or reduction of Fgf8 expression, disrupted several features of HAA patterning, including photoreceptor distribution, ganglion cell density, and organization of interneurons. Notably, patterned expression of RA signaling components was also found in humans, suggesting that RA also plays a role in setting up the human fovea.
高度依赖视觉系统的物种具有一个专门的视网膜区域来支持高敏锐度视觉,例如人类的中央凹。尽管这对我们的日常活动至关重要,但对于驱动视网膜高敏锐度区域(HAA)发育的机制却知之甚少。以鸡作为模型,我们发现成纤维细胞生长因子8(Fgf8)在HAA原基中有精确且动态的表达模式,该模式受降解视黄酸(RA)的酶调控。对RA信号通路进行短暂操作,或降低Fgf8表达,会破坏HAA模式的几个特征,包括光感受器分布、神经节细胞密度和中间神经元的组织。值得注意的是,在人类中也发现了RA信号通路成分的模式化表达,这表明RA在人类中央凹的形成中也发挥作用。