Department of Anatomy and Neurobiology, School of Medicine, Tokyo Women's Medical University, Tokyo, Japan.
Department of Brain and Neuroscience, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan.
J Comp Neurol. 2024 Aug;532(8):e25666. doi: 10.1002/cne.25666.
We have investigated the hippocampal connectivity of the marmoset presubiculum (PreS) and reported that major connections of PreS in the rat were conserved in the marmoset. Moreover, our results indicated the presence of several additional projections that were almost absent in the rat brain, but abundant in the marmoset, such as direct projections from CA1 to PreS. However, little is known about the connectivity between the frontal brain regions and PreS or hippocampal formation. Therefore, we investigated the distribution of cells of the origins and terminals of the presubicular and hippocampal projections in the marmoset frontal brain regions using the retrograde and anterograde tracer cholera toxin B subunit. In cases of tracer injections into all layers of PreS, many neurons and terminals were labeled in the claustrum-endopiriform (Cl-En) complex almost entirely along the rostrocaudal axis. Even in cases where the injection site involved the superficial (not deep) layers of PreS, labeled neurons and terminals were distributed over a wide rostrocaudal range of the Cl-En complex, but their number and density were significantly lower than the whole-layer injection cases. In cases where the injection site was confined to the hippocampal formation, labeled cells and terminals were localized at a restricted portion of the Cl-En complex. Here, we demonstrate for what we believe to be the first time the strong, reciprocal connections of the Cl-En complex with PreS and projections from the Cl-En complex to the hippocampal regions (CA1 and the subiculum) in the marmoset. Our findings indicate that the Cl-En complex may exert a strong influence on the cortical and subcortical outputs from PreS and, in turn, the entire memory circuitry in the marmoset brain.
我们研究了狨猴前下托(PreS)的海马连接,并报告了大鼠前下托的主要连接在狨猴中得到了保留。此外,我们的结果表明存在几种额外的投射,这些投射在大鼠脑中几乎不存在,但在狨猴中却很丰富,例如 CA1 到 PreS 的直接投射。然而,对于额叶脑区与前下托或海马结构之间的连接知之甚少。因此,我们使用逆行和顺行示踪剂霍乱毒素 B 亚单位研究了狨猴额叶脑区中前下托和海马投射的起源和末端细胞的分布。在前下托的所有层注射示踪剂的情况下,许多神经元和末端在屏状核-内嗅皮质复合体(Cl-En 复合体)中被标记,几乎沿着前后轴的全长。即使注射部位涉及前下托的浅层(不包括深层),标记的神经元和末端也分布在 Cl-En 复合体的广泛前后范围内,但它们的数量和密度明显低于全层注射的情况。在注射部位局限于海马结构的情况下,标记的细胞和末端定位于 Cl-En 复合体的一个受限部分。在这里,我们首次证明了 Cl-En 复合体与 PreS 之间的强烈、相互的连接,以及 Cl-En 复合体到海马区域(CA1 和下托)的投射。我们的发现表明,Cl-En 复合体可能对来自 PreS 的皮质和皮质下输出以及狨猴大脑中的整个记忆回路产生强烈影响。