Schoenfeld T A, Macrides F
J Comp Neurol. 1984 Jul 20;227(1):121-35. doi: 10.1002/cne.902270113.
The organization of connections between the main olfactory bulb (MOB) and pars externa (pE) of the anterior olfactory nucleus was studied in hamsters by using wheat germ agglutinin-horseradish peroxidase as both an anterograde and a retrograde neuronal tracer. Bulbar efferents of pE project exclusively to the contralateral MOB. A topographic organization is evident in these efferents, such that distinct sectors of pE project predominantly to certain sectors of the contralateral MOB and lightly to other sectors. The predominant projection to any bulbar sector in the coronal plane is repeated at nearly all rostral-caudal levels, i.e., the pE efferents to the contralateral MOB terminate within long strips or wedges that show a sector-to-sector topographic organization with respect to the medial-lateral and dorsal-ventral axes but not the rostral-caudal axis of the MOB. Afferents to pE arising in the ipsilateral MOB also show a sector-to-sector topographic organization. Injections into restricted sectors along the circumference of pE label all classes of output neurons (mitral cells and internal, middle, and external tufted cells) in restricted sectors of the ipsilateral MOB, and the sectors that have retrograde neuronal labeling are homotopic to those in the contralateral MOB that have dense anterograde terminal labeling. External tufted cells are not labeled and the other classes of MOB output neurons do not have prominent topographic patterns of labeling in cases with injections caudal to pE. The somata of external tufted cell that project to pE are predominantly in the deep part of the glomerular layer; most of the external tufted cells that lie more superficially in the glomerular layer do not appear to have projections extrinsic to the MOB. These results indicate that both the afferent and efferent connections of pE with the MOB are topographically organized and provide a short synaptic pathway between homotopic sectors of the two main olfactory bulbs.
通过使用小麦胚凝集素-辣根过氧化物酶作为顺行和逆行神经元示踪剂,研究了仓鼠主嗅球(MOB)与前嗅核外侧部(pE)之间连接的组织方式。pE的球传出纤维仅投射到对侧MOB。这些传出纤维中存在明显的拓扑组织,使得pE的不同区域主要投射到对侧MOB的某些区域,而对其他区域的投射则较少。在冠状平面上,对任何球部区域的主要投射在几乎所有前后水平都重复出现,即pE到对侧MOB的传出纤维在长条形或楔形区域内终止,这些区域相对于MOB的内外侧和背腹轴呈现区域对区域的拓扑组织,但相对于MOB的前后轴则没有。同侧MOB发出的pE传入纤维也呈现区域对区域的拓扑组织。向pE圆周上的受限区域注射示踪剂,会标记同侧MOB受限区域内的所有类型的输出神经元( mitral细胞以及内、中、外簇状细胞),并且具有逆行神经元标记的区域与对侧MOB中具有密集顺行终末标记的区域是同位的。在pE尾侧注射的情况下,外簇状细胞未被标记,并且其他类型的MOB输出神经元没有明显的拓扑标记模式。投射到pE的外簇状细胞的胞体主要位于肾小球层的深部;肾小球层中位置较浅的大多数外簇状细胞似乎没有MOB以外的投射。这些结果表明,pE与MOB之间的传入和传出连接均具有拓扑组织,并在两个主要嗅球的同位区域之间提供了一条短突触通路。