Mendizabal-Zubiaga Juan L, Reblet Concepcion, Bueno-Lopez Jose L
Department of Neurosciences, School of Medicine and Dentistry, The University of the Basque Country, Vizcaya, Spain.
J Anat. 2007 Aug;211(2):223-36. doi: 10.1111/j.1469-7580.2007.00779.x. Epub 2007 Jul 17.
This paper presents an account of past and current research on spiny inverted neurons--alternatively also known as 'inverted pyramidal neurons'--in rats, rabbits and cats. In our laboratory, we have studied these cells with a battery of techniques suited for light and electron microscopy, including Nissl staining, Golgi impregnation, dye intracellular filling and axon retrograde track-tracing. Our results show that spiny inverted neurons make up less than 8.5 and 5.5% of all cortical neurons in the primary and secondary rabbit visual cortex, respectively. Infragranular spiny inverted neurons constitute 15 and 8.5% of infragranular neurons in the same animal and areas. Spiny inverted neurons congregate at layers V-VI in all studied species. Studies have also revealed that spiny inverted neurons are excitatory neurons which furnish axons for various cortico-cortical, cortico-claustral and cortico-striatal projections, but not for non-telencephalic centres such as the lateral and medial geniculate nuclei, the colliculi or the pons. As a group, each subset of inverted cells contributing to a given projection is located below the pyramidal neurons whose axons furnish the same centre. Spiny inverted neurons are particularly conspicuous as a source of the backward cortico-cortical projection to primary visual cortex and from this to the claustrum. Indeed, they constitute up to 82% of the infragranular cells that furnish these projections. Spiny inverted neurons may be classified into three subtypes according to the point of origin of the axon on the cell: the somatic basal pole which faces the cortical outer surface, the somatic flank and the reverse apical dendrite. As seen with electron microscopy, the axon initial segments of these subtypes are distinct from one another, not only in length and thickness, but also in the number of received synaptic boutons. All of these anatomical features together may support a synaptic-input integration which is peculiar to spiny inverted neurons. In this way, two differently qualified streams of axonal output may coexist in a projection which arises from a particular infragranular point within a given cortical area; one stream would be furnished by the typical pyramidal neurons, whereas spiny inverted neurons would constitute the other source of distinct information flow.
本文介绍了过去和当前对大鼠、兔子和猫体内棘状倒置神经元(也被称为“倒置锥体细胞”)的研究情况。在我们实验室,我们运用了一系列适用于光学和电子显微镜的技术来研究这些细胞,包括尼氏染色、高尔基浸染、染料细胞内填充以及轴突逆行追踪。我们的研究结果表明,在兔初级和次级视觉皮层中,棘状倒置神经元分别占所有皮层神经元的比例不到8.5%和5.5%。在同一动物的相同区域,颗粒下层棘状倒置神经元分别占颗粒下层神经元的15%和8.5%。在所有研究的物种中,棘状倒置神经元聚集在V - VI层。研究还表明,棘状倒置神经元是兴奋性神经元,它们为各种皮质 - 皮质、皮质 - 屏状核和皮质 - 纹状体投射提供轴突,但不为外侧和内侧膝状体核、丘或脑桥等非端脑中心提供轴突。作为一个群体,参与特定投射的每个倒置细胞子集都位于其轴突为同一中心提供轴突的锥体细胞下方。棘状倒置神经元作为向初级视觉皮层以及从初级视觉皮层到屏状核的反向皮质 - 皮质投射的来源尤其显著。事实上,它们构成了提供这些投射的颗粒下层细胞的82%。棘状倒置神经元可根据轴突在细胞上的起源点分为三种亚型:面向皮质外表面的体细胞基极、体细胞侧面和反向顶端树突。从电子显微镜观察来看,这些亚型的轴突起始段不仅在长度和厚度上彼此不同,而且在接受的突触小体数量上也不同。所有这些解剖学特征共同可能支持一种棘状倒置神经元特有的突触输入整合。这样,在源自给定皮质区域内特定颗粒下层点的投射中,可能共存两种不同性质的轴突输出流;一种流由典型的锥体细胞提供,而棘状倒置神经元将构成另一种不同信息流的来源。