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首页> 外文期刊>Journal of Morphology >The dorsal compartment locomotory control system in amphioxus larvae.
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The dorsal compartment locomotory control system in amphioxus larvae.

机译:文昌鱼幼虫的背腔运动控制系统。

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Amphioxus myotomes consist of separate sets of superficial and deep muscle fibers, each with its own innervation, that are thought to be responsible for slow swimming and escape behavior, respectively. Tracings from serial EM sections of the anterior nerve cord in the larva show that the motoneurons and premotor interneurons controlling the superficial fibers (the dorsal compartment, or DC pathway) are linked by specialized junctions of a previously undescribed type, referred to here as juxta-reticular (JR) junctions for the characteristic presence of a cisterna of endoplasmic reticulum on each side. JR junctions link the DC motoneurons with each other, with the largest of the anterior paired neurons (LPN3s) and with one class of ipsilateral projection neurons (IPNs), but occur nowhere else. Because of the paucity of synaptic input to the DC system, larval behavior can only be explained if the JR junctions act as functional links between cells. An analysis of the pattern of cell contacts also suggests that the LPN3s are probably pacemakers for both slow and fast locomotion, but act through junctions in the former case and conventional synapses in the latter. The only major synaptic input to the DC system identified in somites 1 and 2 was from four neurons located in the cerebral vesicle, referred to here as Type 2 preinfundibular projection neurons (PPN2s). They have unusually large varicosities, arranged in series, that make periodic contacts with the DC motoneurons. More caudally, the DC motoneurons receive additional input via similar large varicosities from the receptor cells of the first dorsal ocellus, located in somite 5. The overall circuitry of the locomotory control system suggests that the PPN2s may be instrumental in sustaining slow swimming, whereas mechanical stimulation, especially of the rostrum, preferentially activates the fast mode.
机译:文昌鱼的肌酶由浅层和深层肌肉纤维的独立集合组成,每组纤维都有其自己的神经,分别被认为负责缓慢的游泳和逃逸行为。幼虫前神经索的连续EM切片的描迹表明,控制表层纤维(背侧隔室或DC通路)的运动神经元和运动前神经元通过先前未描述类型的专门连接连接在一起,在这里称为并列连接。网状(JR)交界处,每侧均存在内质网池。 JR接头将DC运动神经元彼此连接,与最大的前对成对神经元(LPN3)和一类同侧投射神经元(IPN)相互连接,但在其他任何地方都没有。由于缺乏向DC系统的突触输入,因此只有在JR接合点充当细胞之间的功能链接时,才能解释幼虫的行为。对细胞接触模式的分析还表明,LPN3可能是慢速和快速运动的起搏器,但在前者情况下通过结点起作用,而在后者情况下通过常规突触起作用。在体节1和2中识别出的DC系统的唯一主要突触输入来自位于大脑囊泡中的四个神经元,此处称为2型漏斗前投射神经元(PPN2s)。它们具有异常大的,连续排列的静脉曲张,周期性地与直流运动神经元接触。更尾部的是,直流运动神经元通过类似的大静脉曲张从位于体节5中的第一个背侧卵母细胞的受体细胞接受额外的输入。运动控制系统的总体电路表明,PPN2可能有助于维持缓慢的游泳,而机械的刺激,特别是对讲台的刺激,会优先激活快速模式。

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