Melchitzky D S, Sesack S R, Pucak M L, Lewis D A
Department of Psychiatry, University of Pittsburgh, Pennsylvania 15213, USA.
J Comp Neurol. 1998 Jan 12;390(2):211-24. doi: 10.1002/(sici)1096-9861(19980112)390:2<211::aid-cne4>3.0.co;2-4.
xũ I sLxxJ In monkey prefrontal cortex, the intrinsic axon collaterals of supragranular pyramidal neurons extend horizontally for considerable distances through the gray matter and give rise to stripe-like clusters of axon terminals (Levitt et al. [1993] J. Comp. Neurol. 338:360-376). Because understanding the functional role of these connections requires knowledge of their synaptic targets, we made injections of biotinylated dextran amine (BDA) into layer 3 of macaque prefrontal area 9 and examined the labeled intrinsic axon collaterals by electron microscopy. Labeled axon terminals formed exclusively asymmetric synapses, and 95.6% of the postsynaptic structures were dendritic spines, presumably belonging to other pyramidal neurons. The remaining postsynaptic structures were dendritic shafts, many of which had the morphological characteristics of local circuit neurons. The prefrontal injections also labeled associational projections that traveled through the white matter to terminate in other areas of prefrontal cortex. All of the synapses formed by these associational axons were asymmetric, and 91.9% were onto dendritic spines. The similarities in synaptic targets of the prefrontal intrinsic and associational axon terminals suggested that these projections might arise from the same neurons, an interpretation confirmed in dual label, retrograde tracing studies. To determine the specificity of the synaptic targets of these prefrontal connections, two additional comparisons were made. In the posterior parietal cortex (area 7a), 94.2% of the synapses furnished by BDA-labeled intrinsic collaterals of supragranular pyramidal neurons were also with dendritic spines. In contrast, only 75.6% of unlabeled asymmetric synapses in the prefrontal cortex were onto dendritic spines. These comparisons suggest that the axons of supragranular pyramidal neurons in primate association cortices are preferentially directed to specific targets. Finally, after injections of BDA, a small number of retrogradely labeled pyramidal neurons were observed within the anterogradely labeled clusters of intrinsic axon terminals. At the ultrastructural level, synapses between anterogradely labeled axon terminals and retrogradely labeled dendritic spines were identified. These findings suggest that reciprocal, monosynaptic connections may exist between pyramidal neurons located in different stripe-like clusters, providing a potential anatomical substrate for reverberating excitatory circuits within the primate association cortices.
在猴前额叶皮层中,颗粒上层锥体神经元的内在轴突侧支在灰质中水平延伸相当长的距离,并形成条纹状的轴突终末簇(Levitt等人,[1993]《比较神经学杂志》338:360 - 376)。由于了解这些连接的功能作用需要知道它们的突触靶点,我们将生物素化葡聚糖胺(BDA)注入猕猴前额叶9区的第3层,并通过电子显微镜检查标记的内在轴突侧支。标记的轴突终末仅形成不对称突触,95.6%的突触后结构是树突棘,推测属于其他锥体神经元。其余的突触后结构是树突干,其中许多具有局部回路神经元的形态特征。前额叶注射还标记了通过白质传导并终止于前额叶皮层其他区域的联合投射。这些联合轴突形成的所有突触都是不对称的,91.9%位于树突棘上。前额叶内在轴突终末和联合轴突终末在突触靶点上的相似性表明这些投射可能来自同一神经元,这一解释在双标记逆行追踪研究中得到证实。为了确定这些前额叶连接的突触靶点的特异性,还进行了另外两项比较。在顶叶后皮层(7a区),颗粒上层锥体神经元的BDA标记的内在侧支提供的突触中,94.2%也与树突棘形成突触。相比之下,前额叶皮层中未标记的不对称突触只有75.6%位于树突棘上。这些比较表明灵长类联合皮层中颗粒上层锥体神经元的轴突优先指向特定靶点。最后,在注射BDA后,在前向标记的内在轴突终末簇内观察到少量逆行标记的锥体神经元。在超微结构水平上,鉴定出前向标记的轴突终末与逆行标记的树突棘之间的突触。这些发现表明位于不同条纹状簇中的锥体神经元之间可能存在相互的单突触连接,为灵长类联合皮层内的兴奋性回路提供了潜在的解剖学基础。