Retinal ganglion cell-derived semaphorin 6A segregates starburst amacrine cell dendritic scaffolds to organize the inner retina.

IF 3.7 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY Development Pub Date : 2024-11-04 DOI:10.1242/dev.204293
Rebecca E James, Natalie R Hamilton, Lola Nicole Huffman, Victoria N Neckles, R. Jeroen Pasterkamp, Loyal A Goff, Alex L Kolodkin
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Abstract

To form functional circuits, neurons must settle in their appropriate cellular locations and then project and elaborate neurites to contact their target synaptic neuropils. Laminar organization within the vertebrate retinal inner plexiform layer (IPL) facilitates pre- and postsynaptic neurite targeting, yet the precise mechanisms underlying establishment of functional IPL subdomains are not well understood. Here we explore mechanisms defining the compartmentalization of OFF and ON neurites generally, and OFF and ON direction-selective neurites specifically, within the developing IPL. We show that semaphorin 6A (Sema6A), a repulsive axon guidance cue, is required for delineation of OFF versus ON circuits within the IPL: in the Sema6a null IPL, the boundary between OFF and ON domains is blurred. Furthermore, Sema6A expressed by retinal ganglion cells (RGCs) directs laminar segregation of OFF and ON starburst amacrine cell (SAC) dendritic scaffolds, which themselves serve as a substrate upon which other retinal neurites elaborate. These results demonstrate that RGCs, the first neuron-type born within the retina, play an active role in functional specialization of the IPL.

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视网膜神经节细胞衍生的半aphorin 6A 可分离星形闪烁的羊膜细胞树突支架,从而组织内视网膜。
为了形成功能性电路,神经元必须在适当的细胞位置定居,然后投射和发育神经元,以接触目标突触神经鞘。脊椎动物视网膜内丛状层(IPL)的层状组织有助于突触前和突触后神经元靶向,但建立 IPL 功能亚域的确切机制还不十分清楚。在这里,我们探讨了在发育中的 IPL 内,一般定义关和通神经元区隔的机制,以及具体定义关和通方向选择性神经元区隔的机制。我们的研究表明,IPL内OFF与ON回路的划分需要semaaphorin 6A(Sema6A)这一排斥性轴突导向线索:在Sema6A无效的IPL中,OFF与ON域之间的界限模糊不清。此外,视网膜神经节细胞(RGC)表达的 Sema6A 还能引导关和开星状突眼细胞(SAC)树突支架的层状分离,而这些树突支架本身又是其他视网膜神经元细化的基质。这些结果表明,RGCs 是视网膜中诞生的第一个神经元类型,在 IPL 的功能特化中发挥着积极作用。
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来源期刊
Development
Development 生物-发育生物学
CiteScore
6.70
自引率
4.30%
发文量
433
审稿时长
3 months
期刊介绍: Development’s scope covers all aspects of plant and animal development, including stem cell biology and regeneration. The single most important criterion for acceptance in Development is scientific excellence. Research papers (articles and reports) should therefore pose and test a significant hypothesis or address a significant question, and should provide novel perspectives that advance our understanding of development. We also encourage submission of papers that use computational methods or mathematical models to obtain significant new insights into developmental biology topics. Manuscripts that are descriptive in nature will be considered only when they lay important groundwork for a field and/or provide novel resources for understanding developmental processes of broad interest to the community. Development includes a Techniques and Resources section for the publication of new methods, datasets, and other types of resources. Papers describing new techniques should include a proof-of-principle demonstration that the technique is valuable to the developmental biology community; they need not include in-depth follow-up analysis. The technique must be described in sufficient detail to be easily replicated by other investigators. Development will also consider protocol-type papers of exceptional interest to the community. We welcome submission of Resource papers, for example those reporting new databases, systems-level datasets, or genetic resources of major value to the developmental biology community. For all papers, the data or resource described must be made available to the community with minimal restrictions upon publication. To aid navigability, Development has dedicated sections of the journal to stem cells & regeneration and to human development. The criteria for acceptance into these sections is identical to those outlined above. Authors and editors are encouraged to nominate appropriate manuscripts for inclusion in one of these sections.
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