Anatomical Sciences and Neurobiology, University of Louisville, Louisville, Kentucky, USA.
J Comp Neurol. 2022 May;530(7):1099-1111. doi: 10.1002/cne.25264. Epub 2021 Oct 24.
Visual pathways of the brain are organized into parallel channels that code different features of the external environment. In the current study, we investigated the anatomical organization of parallel pathways from the superior colliculus (SC) to the pulvinar nucleus in the mouse. Virus injections placed in the ipsilateral and contralateral SC to induce the expression of different fluorescent proteins define two pulvinar zones. The lateral pulvinar (Pl) receives ipsilateral SC input and the caudal medial pulvinar (Pcm) receives bilateral SC input. To examine the ultrastructure of these projections using transmission electron microscopy, we injected the SC with viruses to induce peroxidase expression within synaptic vesicles or mitochondria. We quantitatively compared the sizes of ipsilateral and contralateral tectopulvinar terminals and their postsynaptic dendrites, as well as the sizes of the overall population of synaptic terminals and their postsynaptic dendrites in the Pl and Pcm. Our ultrastructural analysis revealed that ipsilateral tectopulvinar terminals are significantly larger than contralateral tectopulvinar terminals. In particular, the ipsilateral tectopulvinar projection includes a subset of large terminals (≥ 1 μm ) that envelop dendritic protrusions of postsynaptic dendrites. We also found that both ipsilateral and contralateral tectopulvinar terminals are significantly larger than the overall population of synaptic terminals in both the Pl and Pcm. Thus, the ipsilateral tectopulvinar projection is structurally distinct from the bilateral tectopulvinar pathway, but both tectopulvinar channels may be considered the primary or "driving" input to the Pl and Pcm.
大脑的视觉通路组织成平行的通道,这些通道对外部环境的不同特征进行编码。在目前的研究中,我们研究了来自上丘(SC)到小鼠丘脑枕核的平行通路的解剖组织。在同侧和对侧 SC 中注射病毒以诱导不同荧光蛋白的表达,定义了两个丘脑枕核区。外侧丘脑枕核(Pl)接收同侧 SC 的输入,而尾侧内侧丘脑枕核(Pcm)接收双侧 SC 的输入。为了使用透射电子显微镜检查这些投射的超微结构,我们将病毒注射到 SC 中,以诱导突触小泡或线粒体中的过氧化物酶表达。我们定量比较了同侧和对侧顶盖丘脑枕核终末及其突触后树突的大小,以及 Pl 和 Pcm 中整个突触终末及其突触后树突的大小。我们的超微结构分析表明,同侧顶盖丘脑枕核终末明显大于对侧顶盖丘脑枕核终末。特别是,同侧顶盖丘脑枕核投射包括一组较大的终末(≥1μm),这些终末包裹突触后树突的突起。我们还发现,同侧和对侧顶盖丘脑枕核终末都明显大于 Pl 和 Pcm 中整个突触终末群体。因此,同侧顶盖丘脑枕核投射在结构上不同于双侧顶盖丘脑枕核通路,但两者都可能被视为 Pl 和 Pcm 的主要或“驱动”输入。