Bajo Victoria M, Moore David R
University Laboratory of Physiology, University of Oxford, Oxford OX1 3PT, United Kingdom.
J Comp Neurol. 2005 May 30;486(2):101-16. doi: 10.1002/cne.20542.
Corticofugal projections to the auditory midbrain, the inferior colliculus (IC), influence the way in which specific sets of IC neurons process acoustic signals. We used retrograde tracer (Fluorogold, Fluororuby, microbeads) injections in the IC to study the morphology and location of cortico-collicular projecting neurons and anterograde tracer (dextran biotin) injections in auditory cortical fields to describe the distribution of terminals in the IC. Nissl staining, cytochrome oxidase activity, and neurofilament SMI32 immunostaining were used to delimit the different auditory areas. We defined a primary or "core" auditory cortex and a secondary "caudal" auditory area containing layer V pyramidal neurons that project to the IC. These projections target the central nucleus of the IC (CNIC) ipsilaterally and the IC cortices bilaterally, with the ipsilateral component predominant. Other secondary auditory areas, dorsal and ventral to the core, do not directly participate in this projection. The ventral secondary cortex targets midbrain periaqueductal gray. The projection from the core cortex originates from two classes of layer V pyramidal cells. Cells presenting a tufted apical dendrite in layer I have dense terminal fields in the IC cortices. Pyramids lacking layer I dendritic tufts target the CNIC in a less dense but tonotopic manner. The caudal cortex projection originates from smaller layer V pyramids and targets the IC cortices with dense terminal fields. Descending auditory inputs from the core and caudal areas converge in the dorsal and external cortices of the IC. Descending connections to the gerbil IC form a segregated system in which multiple descending channels originating from different neuronal subpopulations may modulate specific aspects of ascending auditory information.
投射到听觉中脑即下丘(IC)的皮质传出纤维,会影响特定组别的IC神经元处理声音信号的方式。我们通过在IC中注射逆行示踪剂(荧光金、荧光红宝石、微珠)来研究皮质 - 丘系投射神经元的形态和位置,并通过在听觉皮质区域注射顺行示踪剂(葡聚糖生物素)来描述IC中终末的分布。尼氏染色、细胞色素氧化酶活性和神经丝SMI32免疫染色被用于界定不同的听觉区域。我们定义了一个初级或“核心”听觉皮质以及一个次级“尾侧”听觉区域,该区域包含投射到IC的第V层锥体神经元。这些投射同侧靶向IC的中央核(CNIC),双侧靶向IC皮质,同侧部分占主导。核心区域背侧和腹侧的其他次级听觉区域不直接参与此投射。腹侧次级皮质靶向中脑导水管周围灰质。来自核心皮质的投射起源于两类第V层锥体细胞。在第I层呈现簇状顶端树突的细胞在IC皮质中有密集的终末场。缺乏第I层树突簇的锥体以密度较低但呈音调拓扑的方式靶向CNIC。尾侧皮质投射起源于较小的第V层锥体,并以密集的终末场靶向IC皮质。来自核心和尾侧区域的下行听觉输入在IC的背侧和外侧皮质汇聚。与沙鼠IC的下行连接形成一个分离的系统,其中源自不同神经元亚群的多个下行通道可能调节上行听觉信息的特定方面。