Mossy fibers in granule cell areas of the rat dorsal cochlear nucleus from intrinsic and extrinsic origin innervate unipolar brush cell glomeruli.

L Alibardi
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Abstract

Non tonotopic transmission between cochlear nuclei and other auditory and non-auditory nuclei in the brain is probably due to large axonal terminals (mossy fibers) innervating granule cell areas of cochlear nuclei. The origin of mossy fibers in the dorsal cochlear nucleus (DCN) is multiple, from other auditory or non-auditory nuclei but possibly also from intrinsic neurons. The present ultrastructural immunocytochemical study reports for the first time the presence of anterograde-labeled mossy fibers in the DCN of the rat after injection of the neural tracer WGA-HRP into 3 different nuclei. Labeled mossy fibers were seen in 9.0% of mossy fibers detected after tracer injection into the ipsilateral anteroventral cochlear nucleus, in 7.3% of mossy fibers after contralateral collicular injection, and 13.2% after contralateral cochlear nucleus injection. Most (over 95%) mossy fibers contained round vesicles, both large and small, and were likely excitatory terminals, but few showed flat-pleomorphic vesicles that contained the inhibitory neurotransmitters GABA and glycine. Most of the anterograde-labeled ipsilateral mossy fibers containing small round synaptic vesicles, are probably derived from multipolar neurons within the ipsilateral anteroventral cochlear nucleus. After injections into the contralateral inferior colliculus, it was not possible to distinguish putative descending collicular mossy fibers from intrinsic mossy fibers. The latter would suggest the presence of an amplification pathway within the DCN, from collateral axons of pyramidal or stellate cells of the ipsilateral ventral cochlear nucleus to form glomeruli with granule-unipolar brush cells. After injection into the contralateral cochlear nucleus, it was not possible to distinguish between commissural mossy fibers and those derived from ipsilateral recurrent axon-terminals of commissural neurons within the DCN or the ventral cochlear nucleus. Despite this limitation, the present observations show that extrinsic or intrinsic mossy fibers reach granule cell areas in layers 2 and 3 of the DCN and form glomeruli of large or small dimension (1.5-4 microm) with unipolar brush and granule cells. These mossy fibers probably carry a fast excitatory non-tonotopic input which may influence the electrical response of granule cell areas.

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大鼠耳蜗背核颗粒细胞区来自内源性和外源性的苔藓纤维支配单极刷状细胞肾小球。
耳蜗核与脑内其他听核和非听核之间的非张力传递可能是由于大轴突终末(苔藓状纤维)支配耳蜗核的颗粒细胞区。耳蜗背核(DCN)苔藓纤维的来源是多方面的,可能来自其他听核或非听核,也可能来自内在神经元。本研究首次报道了神经示踪剂WGA-HRP注入3种不同的细胞核后,大鼠DCN中出现顺行标记的苔藓纤维。同侧耳蜗前腹侧核注射示踪剂检测到的苔藓纤维中有标记的占9.0%,对侧耳蜗颈注射示踪剂检测到的苔藓纤维中有标记的占7.3%,对侧耳蜗核注射示踪剂检测到的苔藓纤维中有标记的占13.2%。大多数(95%以上)苔藓纤维含有大大小小的圆形囊泡,可能是兴奋性末梢,但少数呈扁平多形性囊泡,含有抑制性神经递质GABA和甘氨酸。大多数顺行标记的同侧苔藓状纤维含有小的圆形突触囊泡,可能来自同侧耳蜗前腹侧核内的多极神经元。注射到对侧下丘后,无法区分推定的降丘苔藓纤维和固有的苔藓纤维。后者可能表明DCN内存在扩增途径,从同侧耳蜗腹侧核锥体细胞或星状细胞的侧侧轴突到颗粒单极刷状细胞形成肾小球。注射到对侧耳蜗核后,无法区分互交苔藓状纤维和来自DCN内同侧互交神经元的复发轴突末梢或耳蜗腹侧核的苔藓状纤维。尽管存在这种限制,但目前的观察表明,外源性或内源性苔藓纤维可到达DCN第2层和第3层的颗粒细胞区域,并形成具有单极刷状和颗粒细胞的大小肾小球(1.5-4微米)。这些苔藓状纤维可能携带快速兴奋的非张力输入,这可能影响颗粒细胞区域的电反应。
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