Department of Molecular Medicine, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Kavli Institute for Systems Neuroscience and Center for Biology of Memory, Norwegian University of Science and Technology, Trondheim, Norway.
Hippocampus. 2022 Sep;32(9):639-659. doi: 10.1002/hipo.23457. Epub 2022 Aug 1.
The hippocampal formation is essential for spatial navigation and episodic memory. The anatomical structure is largely similar across mammalian species, apart from the deep polymorphic layer of the dentate gyrus and the adjacent part of cornu ammonis 3 (CA3) which feature substantial variations. In rodents, the polymorphic layer has a triangular cross-section abutting on the end of the CA3 pyramidal layer, while in primates it is long and band-shaped capping the expanded CA3 end, which here lacks a distinct pyramidal layer. This structural variation has resulted in a confusing nomenclature and unclear anatomical criteria for the definition of the dentate-ammonic border. Seeking to clarify the border, we present here a light microscopic investigation based on Golgi-impregnated and Timm-thionin-stained sections of the Artiodactyla sheep and domestic pig, in which the dentate gyrus and CA3 end have some topographical features in common with primates. In short, the band-shaped polymorphic layer coincides with the Timm-positive mossy fiber collateral plexus and the Timm-negative subgranular zone. While the soma and excrescence-covered proximal dendrites of the mossy cells are localized within the plexus, the peripheral mossy cell dendrites extend outside the plexus, both into the granular and molecular layers, and the CA3. The main mossy fibers leave the collateral plexus in a scattered formation to converge gradually through the CA3 end in between the dispersed pyramidal cells, which are of three subtypes, as in monkey, with the classical apical subtype dominating near the hidden blade, the nonapical subtype near the exposed blade, and the dentate subtype being the only pyramidal cells that extend dendrites into the dentate gyrus. In agreement with our previous study in mink, the findings show that the border between the dentate gyrus and the CA3 end can be more accurately localized by the mossy fiber system than by cyto-architecture alone.
海马结构对于空间导航和情景记忆至关重要。除了齿状回的深多形层和毗邻的角回 3 区(CA3)部分有实质性变化外,其解剖结构在哺乳动物中基本相似。在啮齿动物中,多形层呈三角形,毗邻 CA3 锥体层的末端,而在灵长类动物中,它呈长形且带状,覆盖在扩展的 CA3 末端,这里没有明显的锥体层。这种结构上的差异导致了混乱的命名法和不明确的解剖标准,难以定义齿状回-角回边界。为了阐明边界,我们在此展示了基于偶蹄目绵羊和家猪的高尔基浸渍和 Timm-硫堇染色切片的显微镜研究,其中齿状回和 CA3 末端具有一些与灵长类动物相似的拓扑特征。简而言之,带状多形层与 Timm 阳性苔藓纤维侧支丛和 Timm 阴性颗粒下区吻合。虽然苔藓细胞的体部和生有棘突的近端树突定位于丛内,但外周的苔藓细胞树突延伸到丛外,进入颗粒层和分子层以及 CA3。主要的苔藓纤维离开侧支丛后呈散射状,在 CA3 末端逐渐汇聚,散布在其间的锥体细胞之间,这些锥体细胞有三种亚型,与猴子中的相同,具有经典的顶侧亚型,主要分布在隐蔽叶附近,非顶侧亚型主要分布在暴露叶附近,而齿状亚型是唯一将树突延伸到齿状回的锥体细胞。与我们之前在貂中的研究结果一致,这些发现表明,苔藓纤维系统比细胞结构本身更能准确地定位齿状回和 CA3 末端之间的边界。