Arimatsu Y, Nihonmatsu I, Hirata K, Takiguchi-Hayashi K
Laboratory of Neuromorphology, Mitsubishi Kasei Institute of Life Sciences, Tokyo, Japan.
J Neurosci. 1994 Apr;14(4):2020-31. doi: 10.1523/JNEUROSCI.14-04-02020.1994.
Monoclonal antibody PC3.1 detects a unique subpopulation of neurons located mainly in layer VI and, to a lesser extent, in layer V within the lateral neocortical areas in the rat. In an attempt to characterize these neurons, we determined the time of their generation in selected neocortical areas by a double-labeling experiment combining quantitative long-survival 3H-thymidine autoradiography and immunohistochemistry for the PC3.1 antigen. We found that the vast majority of PC3.1-positive neurons in both layers V and VI were generated concurrently at embryonic day 15 in all areas examined, demonstrating a strict correlation between the molecular identity of neurons and the time of their generation, irrespective of their final positions along the radial and tangential axes. In contrast, PC3.1-negative neurons, which should represent more diverse phenotypic identities, were generated during a more extended period of cortical development and tended to exhibit radial (inside-to-outside) and tangential (ventral-to-dorsal and rostral-to-caudal) neurogenetic gradients. Our findings indicate that laminar and tangential locations of cortical neurons are not established solely by a combination of mechanisms for the inside-out movement of newly generated neurons in each cortical area and for the broad tangential neurogenetic gradients. The results of this study suggest a distinct way of cortical development in which neurons with a common molecular phenotype are generated concurrently and migrate toward their eventual positions, which are not necessarily located in a single lamina. In addition, our results suggest some kind of tangential heterogeneity in the mechanism involved in neocortical histogenesis, supporting the concept of early regional specification within the neocortex.
单克隆抗体PC3.1可检测到一类独特的神经元亚群,主要位于大鼠外侧新皮质区域的VI层,在V层中的数量较少。为了对这些神经元进行特征描述,我们通过定量长期存活的3H-胸腺嘧啶放射自显影术与PC3.1抗原免疫组织化学相结合的双标记实验,确定了它们在选定新皮质区域的生成时间。我们发现,在所有检查区域中,V层和VI层中绝大多数PC3.1阳性神经元均在胚胎第15天同时生成,这表明神经元的分子特性与其生成时间之间存在严格的相关性,而与其沿径向和切向轴的最终位置无关。相比之下,PC3.1阴性神经元,它们应代表更多样化的表型特征,在皮质发育的更长时期内生成,并且倾向于表现出径向(由内向外)和切向(腹侧到背侧以及嘴侧到尾侧)的神经发生梯度。我们的研究结果表明,皮质神经元的层状和切向位置并非仅由每个皮质区域中新生成神经元的由内向外移动机制与广泛的切向神经发生梯度的组合来确定。本研究结果提示了一种独特的皮质发育方式,即具有共同分子表型的神经元同时生成并迁移至其最终位置,这些位置不一定位于单一层中。此外,我们的结果提示在新皮质组织发生所涉及的机制中存在某种切向异质性,支持了新皮质内早期区域特化的概念。