Department of Ophthalmology and Stein Eye Institute, David Geffen School of Medicine at University of California Los Angeles, Los Angeles, CA 90095.
McGovern Institute for Brain Research, Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139.
Proc Natl Acad Sci U S A. 2024 Apr 16;121(16):e2313820121. doi: 10.1073/pnas.2313820121. Epub 2024 Apr 10.
In primates, high-acuity vision is mediated by the fovea, a small specialized central region of the retina. The fovea, unique to the anthropoid lineage among mammals, undergoes notable neuronal morphological changes during postnatal maturation. However, the extent of cellular similarity across anthropoid foveas and the molecular underpinnings of foveal maturation remain unclear. Here, we used high-throughput single-cell RNA sequencing to profile retinal cells of the common marmoset (), an early divergent in anthropoid evolution from humans, apes, and macaques. We generated atlases of the marmoset fovea and peripheral retina for both neonates and adults. Our comparative analysis revealed that marmosets share almost all their foveal types with both humans and macaques, highlighting a conserved cellular structure among primate foveas. Furthermore, by tracing the developmental trajectory of cell types in the foveal and peripheral retina, we found distinct maturation paths for each. In-depth analysis of gene expression differences demonstrated that cone photoreceptors and Müller glia (MG), among others, show the greatest molecular divergence between these two regions. Utilizing single-cell ATAC-seq and gene-regulatory network inference, we uncovered distinct transcriptional regulations differentiating foveal cones from their peripheral counterparts. Further analysis of predicted ligand-receptor interactions suggested a potential role for MG in supporting the maturation of foveal cones. Together, these results provide valuable insights into foveal development, structure, and evolution.
在灵长类动物中,高敏锐度视觉由黄斑(fovea)介导,黄斑是视网膜的一个小型中央特化区域。黄斑是灵长类动物在哺乳动物中的独特结构,在出生后成熟过程中经历了显著的神经元形态变化。然而,灵长类动物黄斑之间的细胞相似性程度以及黄斑成熟的分子基础仍不清楚。在这里,我们使用高通量单细胞 RNA 测序来描绘普通狨猴(Callithrix jacchus)的视网膜细胞,普通狨猴是灵长类动物进化中与人类、猿和猕猴早期分化的物种。我们为新生儿和成年普通狨猴的黄斑和周边视网膜生成了图谱。我们的比较分析表明,普通狨猴与人类和猕猴共享几乎所有的黄斑类型,突出了灵长类动物黄斑之间的细胞结构的保守性。此外,通过追踪黄斑和周边视网膜中细胞类型的发育轨迹,我们发现每个区域都有独特的成熟路径。对基因表达差异的深入分析表明,视锥细胞和 Muller 胶质细胞(Müller glia,MG)等在这两个区域之间表现出最大的分子差异。利用单细胞 ATAC-seq 和基因调控网络推断,我们揭示了区分黄斑和周边视锥细胞的不同转录调控。对预测的配体-受体相互作用的进一步分析表明,MG 可能在支持黄斑视锥细胞成熟方面发挥作用。总之,这些结果为黄斑发育、结构和进化提供了有价值的见解。