Department of Neurobiology
Brain Research Institute, David Geffen School of Medicine at the University of California, Los Angeles, Los Angeles, California 90095.
J Neurosci. 2021 Feb 3;41(5):991-1004. doi: 10.1523/JNEUROSCI.2455-20.2020. Epub 2020 Dec 2.
Mossy cells (MCs) of the dentate gyrus (DG) are a major group of excitatory hilar neurons that are important for regulating activity of dentate granule cells. MCs are particularly intriguing because of their extensive longitudinal connections within the DG. It has generally been assumed that MCs in the dorsal and ventral DG have similar patterns of termination in the inner one-third of the dentate molecular layer. Here, we demonstrate that axonal projections of MCs in these two regions are considerably different. MCs in dorsal and ventral regions were labeled selectively with Cre-dependent eYFP or mCherry, using two transgenic mouse lines (including both sexes) that express Cre-recombinase in MCs. At four to six weeks following unilateral labeling of MCs in the ventral DG, a dense band of fibers was present in the inner one-fourth of the molecular layer and extended bilaterally throughout the rostral-caudal extent of the DG, replicating the expected distribution of MC axons. In contrast, following labeling of MCs in the dorsal DG, the projections were more diffusely distributed. At the level of transfection, fibers were present in the inner molecular layer, but they progressively expanded into the middle molecular layer and, most ventrally, formed a distinct band in this region. Optical stimulation of these caudal fibers expressing ChR2 demonstrated robust EPSCs in ipsilateral granule cells and enhanced the effects of perforant path stimulation in the ventral DG. These findings suggest that MCs in the dorsal and ventral DG differ in the distribution of their axonal projections and possibly their function. Mossy cells (MCs), a major cell type in the hilus of the dentate gyrus (DG), are unique in providing extensive longitudinal and commissural projections throughout the DG. Although it has been assumed that all MCs have similar patterns of termination in the inner molecular layer of the DG, we discovered that the axonal projections of dorsal and ventral MCs differ. While ventral MC projections exhibit the classical pattern, with dense innervation in the inner molecular layer, dorsal MCs have a more diffuse distribution and expand into the middle molecular layer where they overlap and interact with innervation from the perforant path. These distinct locations and patterns of axonal projections suggest that dorsal and ventral MCs may have different functional roles.
齿状回(DG)的苔状细胞(MCs)是兴奋性门区神经元的主要群体,对调节颗粒细胞的活动具有重要意义。MCs 非常有趣,因为它们在 DG 内具有广泛的纵向连接。通常认为,DG 背侧和腹侧的 MCs 在 DG 内 1/3 分子层的内缘具有相似的终止模式。在这里,我们证明了这两个区域的 MC 轴突投射有很大的不同。使用两种在 MCs 中表达 Cre 重组酶的转基因小鼠系(包括雌雄),通过 Cre 依赖性 eYFP 或 mCherry 选择性标记 DG 背侧和腹侧的 MCs。在腹侧 DG 的 MCs 单侧标记后 4 到 6 周,在分子层的内 1/4 存在致密的纤维带,并在 DG 的前后向延伸到双侧,复制了 MC 轴突的预期分布。相比之下,在标记 DG 背侧的 MCs 后,投射更加弥散。在转染水平,纤维存在于内分子层,但它们逐渐扩展到中间分子层,最腹侧在该区域形成一个明显的带。对表达 ChR2 的这些尾部纤维进行光刺激,在同侧颗粒细胞中产生强大的 EPSC,并增强 DG 腹侧的穿通路径刺激的效果。这些发现表明,DG 背侧和腹侧的 MCs 在其轴突投射的分布和可能的功能上存在差异。Mossy cells (MCs),是齿状回(DG)门区的主要细胞类型,其独特之处在于提供广泛的 DG 纵向和连合性投射。尽管人们一直认为所有的 MCs 在 DG 的内分子层都有相似的终止模式,但我们发现 DG 背侧和腹侧 MCs 的轴突投射不同。虽然腹侧 MC 的投射呈现出典型的模式,在分子层内有密集的神经支配,但背侧 MC 则有更弥散的分布,并扩展到中间分子层,在那里它们与来自穿通路径的神经支配重叠和相互作用。这些不同的位置和轴突投射模式表明,背侧和腹侧 MCs 可能具有不同的功能作用。