O'Leary D D, Stanfield B B
Department of Neurology, Washington University School of Medicine, St. Louis, Missouri 63110.
J Neurosci. 1989 Jul;9(7):2230-46. doi: 10.1523/JNEUROSCI.09-07-02230.1989.
In adult rats, cortical neurons that extend an exon through the pyramidal tract (a major subcortical efferent projection of the neocortex) are limited to layer V of about the rostral two-thirds of the neocortex. In neonates, however, pyramidal tract neurons are distributed throughout the neocortex, but all of those found in certain areas, such as the posterior occipital region (including primary visual cortex) selectively lose their pyramidal tract axon (Stanfield et al., 1982) yet maintain axon collaterals to other subcortical targets (O'Leary and Stanfield, 1985). To determine if the regional location of a developing pyramidal tract neuron critically influences the maintenance or elimination of the axon collaterals it initially extends, pieces of cortex from embryonic day 17 (E17) rat fetuses (exposed to 3H-thymidine on E15) were transplanted heterotopically into the cortex of newborn (PO) rats; rostral cortex was placed into the posterior occipital region (R----O), or posterior occipital cortex into a rostral cortical locale (O----R). The retrograde tracers Fast blue (FB) and Diamidino yellow (DY) were used to assay for the presence of specific populations of cortical projection neurons within the autoradiographically identified transplants. In terms of the extension and maintenance of pyramidal tract axons, the transplanted neurons behave like the host neurons of the recipient cortical region rather than like those of their site of origin. At P40, following FB injections into the pyramidal decussation on P34, pyramidal tract neurons are labeled within the O----R transplants, but none can be labeled within R----O transplants, although in the same R----O cases transplanted neurons are labeled by an injection of DY in the superior colliculus. However, at P13 pyramidal tract neurons can be identified within the R----O transplants, as well as in the host occipital cortex, following injections made on P9, a period when the distribution of pyramidal tract neurons in normal rats is widespread (Stanfield and O'Leary, 1985b). In a second series of host rats, on P34 FB was injected in the pyramidal decussation of the O----R cases, or in the superior colliculus of the R----O cases, and in both groups DY was injected into the region of contralateral cortex homotopic for the new location of the transplant. On P40, in both the O----R and R----O transplants, many neurons singly labeled with FB or DY are found, but no double dye-labeled cells are seen.(ABSTRACT TRUNCATED AT 400 WORDS)
在成年大鼠中,轴突穿过锥体束(新皮层主要的皮质下传出投射)的皮质神经元仅限于新皮层约前三分之二的V层。然而,在新生大鼠中,锥体束神经元分布于整个新皮层,但在某些区域(如枕后区,包括初级视觉皮层)发现的所有这些神经元会选择性地失去其锥体束轴突(斯坦菲尔德等人,1982年),但仍保留至其他皮质下靶点的轴突侧支(奥利里和斯坦菲尔德,1985年)。为了确定发育中的锥体束神经元的区域位置是否对其最初延伸的轴突侧支的维持或消除有至关重要的影响,将胚胎第17天(E17)大鼠胎儿(在E15时暴露于3H - 胸腺嘧啶)的皮质片异位移植到新生(出生后第0天,PO)大鼠的皮质中;将前侧皮质置于枕后区(R→O),或将枕后皮质置于前侧皮质区域(O→R)。使用逆行示踪剂快蓝(FB)和双脒基黄(DY)来检测放射自显影鉴定的移植组织中特定皮质投射神经元群体的存在。就锥体束轴突的延伸和维持而言,移植的神经元表现得像受体皮质区域的宿主神经元,而不像其起源部位的神经元。在出生后第40天,在出生后第34天向锥体交叉注射FB后,在O→R移植组织中可标记出锥体束神经元,但在R→O移植组织中未发现可标记的神经元,尽管在相同的R→O移植组织中,通过向上丘注射DY可标记移植的神经元。然而,在出生后第13天,在出生后第9天注射后,在R→O移植组织以及宿主枕叶皮质中均可鉴定出锥体束神经元,此时正常大鼠中锥体束神经元的分布很广泛(斯坦菲尔德和奥利里,1985b)。在第二组宿主大鼠中,在出生后第34天,向O→R移植组织的锥体交叉或R→O移植组织的上丘注射FB,并在两组中向与移植新位置同位的对侧皮质区域注射DY。在出生后第40天,在O→R和R→O移植组织中均发现了许多单独用FB或DY标记的神经元,但未见到双染料标记的细胞。(摘要截断于400字)