De Carlos J A, O'Leary D D
Molecular Neurobiology Laboratory, Salk Institute for Biological Studies, La Jolla, California 92037.
J Neurosci. 1992 Apr;12(4):1194-211. doi: 10.1523/JNEUROSCI.12-04-01194.1992.
In the developing mammalian neocortex, the first postmitotic neurons form the "preplate" superficial to the neuroepithelium. The preplate is later split into a marginal zone (layer 1) and subplate by cortical plate neurons that form layers 2-6. Cortical efferent axons from layers 5 and 6 and cortical afferent axons from thalamus pass between cortex and subcortical structures through the internal capsule. Here, we identify in rats the axonal populations that establish the internal capsule, and characterize the potential role of subplate axons in the development of cortical efferent and afferent projections. The early growth of cortical efferent and afferent axons was studied using 1-1'-dioctodecyl-3,3,3',3'-tetramethylindocarbocyanine perchlorate (Dil) as an anterograde and retrograde tracer in aldehyde-fixed brains of embryonic rats. Cortical axons first enter the nascent internal capsule on embryonic day (E) 14 and originate from lateral and anterior cortex; axons from posterior cortex extend rostrally but do not yet exit cortex. The labeled axons, tipped by growth cones with complex morphologies, take a pathway deep to the preplate. Preplate neurons extend these early cortical efferents, based on the developmental stage of the cortex, and on their location and morphology. Most of these cells later occupy the subplate. Cortical plate neurons extend axons into the internal capsule by E16. En route to the internal capsule, cortical plate axons take the same path as the earlier-growing preplate axons, through the intermediate zone deep to subplate. Subplate axons reach thalamus by E16; the first cortical plate axons enter thalamus about a day later. Thalamic axons enter cortex by E16, prior to other cortical afferents. On E15, both preplate and thalamic axons reach the midpoint of the internal capsule. To determine the subcortical distribution of subplate axons, we used Dil as a retrograde tracer in aldehyde-fixed brains and fast blue and rhodamine-B-isothiocyanate as in vivo retrograde markers in neonatal rats. Tracers were injected into the superior colliculus, the principal midbrain target of layer 5 neurons, at times before, during, and after the arrival of cortical axons, or into the subcortical pathway of primary layer 5 axons at two points, the cerebral peduncle caudal to the internal capsule, and the pyramidal decussation at the junction of the hindbrain and spinal cord, at times shortly after the passing of cortical axons. In every case, the labeled neurons are confined to layer 5; subplate neurons are not labeled.(ABSTRACT TRUNCATED AT 400 WORDS)
在发育中的哺乳动物新皮层中,首批有丝分裂后的神经元在神经上皮浅层形成“前板”。随后,前板被形成第2 - 6层的皮质板神经元分裂为边缘区(第1层)和亚板。来自第5层和第6层的皮质传出轴突以及来自丘脑的皮质传入轴突通过内囊在皮层和皮层下结构之间穿行。在此,我们在大鼠中鉴定出形成内囊的轴突群体,并描述亚板轴突在皮质传出和传入投射发育中的潜在作用。利用1 - 1'-二辛基-3,3,3',3'-四甲基吲哚羰花青高氯酸盐(Dil)作为顺行和逆行示踪剂,在胚胎大鼠的醛固定脑中研究皮质传出和传入轴突的早期生长。皮质轴突在胚胎第14天首次进入新生内囊,起源于外侧和前部皮质;来自后部皮质的轴突向前延伸但尚未穿出皮质。带有复杂形态生长锥的标记轴突走一条在前板深层的路径。根据皮层的发育阶段、前板神经元的位置和形态,前板神经元延伸这些早期皮质传出轴突。这些细胞中的大多数后来占据亚板。到胚胎第16天,皮质板神经元将轴突延伸至内囊。在通向内囊的途中,皮质板轴突与早期生长的前板轴突走相同路径,穿过亚板深层的中间区。亚板轴突在胚胎第16天到达丘脑;第一批皮质板轴突大约在一天后进入丘脑。丘脑轴突在胚胎第16天进入皮质,早于其他皮质传入纤维。在胚胎第15天,前板和丘脑轴突都到达内囊中点。为了确定亚板轴突的皮层下分布,我们在醛固定脑中使用Dil作为逆行示踪剂,并在新生大鼠中使用快蓝和异硫氰酸罗丹明B作为体内逆行标记物。在皮质轴突到达之前、期间和之后的不同时间,将示踪剂注入上丘(第5层神经元的主要中脑靶区),或者在皮质轴突通过后不久,在两个点——内囊尾侧的大脑脚以及后脑与脊髓交界处的锥体交叉,将示踪剂注入第5层主要轴突的皮层下通路。在每种情况下,标记的神经元都局限于第层;亚板神经元未被标记。(摘要截选至400字)