Kaneko T, Caria M A, Asanuma H
Laboratory of Motor Physiology, Rockefeller University, New York, NY 10021.
J Comp Neurol. 1994 Jul 8;345(2):172-84. doi: 10.1002/cne.903450203.
Connections between motor cortical neurons receiving somatosensory inputs from area 2 and large pyramidal cells in layer V were examined in the cat via intracellular injection of biocytin and immunohistochemistry of nonphosphorylated neurofilament proteins (npNFP). Biocytin was injected into pyramidal cells in layers II/III of the motor cortex that responded monosynaptically and polysynaptically to microstimulation of the somatosensory cortex and subsequently stained black by the avidin-biotinylated peroxidase complex method with diaminobenzidine (DAB) and nickel. By using a monoclonal antibody SMI-32 and a modified peroxidase-antiperoxidase method with Tris-aminophenyl-methane (TAPM) and p-cresol as a chromogen, pyramidal cells in layers III and V of the motor cortex were stained red for npNFP. In particular, all the large pyramidal cells in layer V, Betz cells, displayed intense npNFP immunoreactivity not only in the perikarya but also in the dendrites. Double staining with DAB/nickel and TAPM/p-cresol showed that biocytin-filled axon varicosities of the pyramidal cells, which were thought to receive monosynaptic inputs from area 2, made contacts with npNFP-positive dendrites in layers I-III around the biocytin-injected cell and in layers V-VI beneath the cell. The present results suggest that the corticocortical input from area 2 to pyramidal cells in layers II/III of the motor cortex is transferred to layer V pyramidal cells, including Betz cells, as well as to neighboring layer II/III pyramidal cells. Since tetanic stimulation of the somatosensory cortex reportedly produces long-term potentiation in layer II/III cells of the motor cortex, it seems reasonable to assume that a given area of the somatosensory cortex can produce a long-lasting change in the activity of a given group of output cells in the motor cortex.
通过向猫体内细胞内注射生物素,并对非磷酸化神经丝蛋白(npNFP)进行免疫组织化学分析,研究了接受来自2区体感输入的运动皮层神经元与V层大锥体细胞之间的连接。将生物素注射到运动皮层II/III层的锥体细胞中,这些细胞对体感皮层的微刺激产生单突触和多突触反应,随后用抗生物素蛋白-生物素化过氧化物酶复合物方法,以二氨基联苯胺(DAB)和镍将其染成黑色。使用单克隆抗体SMI-32以及改良的过氧化物酶-抗过氧化物酶方法,以三氨基苯基甲烷(TAPM)和对甲酚作为显色剂,运动皮层III层和V层的锥体细胞被染成红色以显示npNFP。特别是,V层中的所有大锥体细胞,即贝茨细胞,不仅在胞体中,而且在树突中都显示出强烈的npNFP免疫反应性。用DAB/镍和TAPM/对甲酚进行双重染色表明,被认为接受来自2区单突触输入的锥体细胞的生物素填充轴突膨体,与注射生物素细胞周围I-III层以及细胞下方V-VI层中npNFP阳性树突形成接触。目前的结果表明,从2区到运动皮层II/III层锥体细胞的皮质-皮质输入被传递到V层锥体细胞,包括贝茨细胞,以及相邻的II/III层锥体细胞。由于据报道,对体感皮层的强直刺激会在运动皮层的II/III层细胞中产生长时程增强,因此可以合理地假设,体感皮层的特定区域可以在运动皮层中给定的一组输出细胞的活动中产生持久变化。