Dillingham Christopher H, Gay Sean M, Behrooz Roxana, Gabriele Mark L
Department of Biology, James Madison University, Harrisonburg, Virginia.
J Comp Neurol. 2017 Dec 1;525(17):3742-3756. doi: 10.1002/cne.24300. Epub 2017 Aug 17.
The complex neuroanatomical connections of the inferior colliculus (IC) and its major subdivisions offer a juxtaposition of segregated processing streams with distinct organizational features. While the tonotopically layered central nucleus is well-documented, less is known about functional compartments in the neighboring lateral cortex (LCIC). In addition to a laminar framework, LCIC afferent-efferent patterns suggest a multimodal mosaic, consisting of a patchy modular network with surrounding extramodular domains. This study utilizes several neurochemical markers that reveal an emerging LCIC modular-extramodular microarchitecture. In newborn and post-hearing C57BL/6J and CBA/CaJ mice, histochemical and immunocytochemical stains were performed for acetylcholinesterase (AChE), nicotinamide adenine dinucleotide phosphate-diaphorase (NADPH-d), glutamic acid decarboxylase (GAD), cytochrome oxidase (CO), and calretinin (CR). Discontinuous layer 2 modules are positive for AChE, NADPH-d, GAD, and CO throughout the rostrocaudal LCIC. While not readily apparent at birth, discrete cell clusters emerge over the first postnatal week, yielding an identifiable modular network prior to hearing onset. Modular boundaries continue to become increasingly distinct with age, as surrounding extramodular fields remain largely negative for each marker. Alignment of modular markers in serial sections suggests each highlight the same periodic patchy network throughout the nascent LCIC. In contrast, CR patterns appear complementary, preferentially staining extramodular LCIC zones. Double-labeling experiments confirm that NADPH-d, the most consistent developmental modular marker, and CR label separate, nonoverlapping LCIC compartments. Determining how this emerging modularity may align with similar LCIC patch-matrix-like Eph/ephrin guidance patterns, and how each interface with, and potentially influence developing multimodal LCIC projection configurations is discussed.
下丘(IC)及其主要亚区复杂的神经解剖连接提供了具有不同组织特征的分离处理流的并置。虽然音调拓扑分层的中央核有充分的文献记载,但关于相邻外侧皮质(LCIC)中的功能区室却知之甚少。除了分层框架外,LCIC的传入-传出模式表明存在一个多模态镶嵌结构,由一个斑块状模块化网络及其周围的模块外区域组成。本研究使用了几种神经化学标记物,揭示了一种新出现的LCIC模块化-模块外微结构。在新生和听力后的C57BL/6J和CBA/CaJ小鼠中,对乙酰胆碱酯酶(AChE)、烟酰胺腺嘌呤二核苷酸磷酸黄递酶(NADPH-d)、谷氨酸脱羧酶(GAD)、细胞色素氧化酶(CO)和钙视网膜蛋白(CR)进行了组织化学和免疫细胞化学染色。在整个前后向的LCIC中,不连续的第2层模块对AChE、NADPH-d、GAD和CO呈阳性。虽然在出生时不太明显,但离散的细胞簇在出生后的第一周出现,在听力开始前形成一个可识别的模块化网络。随着年龄的增长,模块化边界变得越来越明显,因为周围的模块外区域对每种标记物大多呈阴性。连续切片中模块化标记物的对齐表明,每个标记物在整个新生LCIC中都突出显示相同的周期性斑块状网络。相比之下,CR模式似乎是互补的,优先对模块外的LCIC区域进行染色。双重标记实验证实,NADPH-d是最一致的发育模块化标记物,与CR标记不同的、不重叠的LCIC区室。本文讨论了这种新出现的模块化如何与类似的LCIC斑块-基质样Eph/ephrin引导模式对齐,以及每个模块如何与发育中的多模态LCIC投射配置相互作用并可能对其产生影响。