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胚胎期鸡(家鸡)基板前体消融后结状神经节的代偿反应及发育

Compensatory responses and development of the nodose ganglion following ablation of placodal precursors in the embryonic chick (Gallus domesticus).

作者信息

Harrison T A, Stadt H A, Kumiski D, Kirby M L

机构信息

Department of Cellular Biology and Anatomy, Medical College of Georgia, Augusta 30912-2000, USA.

出版信息

Cell Tissue Res. 1995 Aug;281(2):379-85. doi: 10.1007/BF00583407.

Abstract

The nodose ganglion is the distal cranial ganglion of the vagus nerve which provides sensory innervation to the heart and other viscera. In this study, removal of the neuronal precursors which normally populate the right nodose ganglion was accomplished by ablating the right nodose placode in stage 9 chick embryos. Subsequent histological evaluation showed that in 54% of lesioned embryos surviving to day 6, the right ganglion was absent. Most embryos surviving to day 12, however, had identifiable right ganglia. In day 12 embryos, the right ganglion which developed was abnormal, with ganglion volume and ganglion cell diameter reduced by 50% and 20%, respectively, compared to control ganglia. To investigate the source of the neuron population in the regenerated ganglion, we combined nodose placode ablation with bilateral replacement of chick with quail "cardiac" neural crest (from mid-otic placode to somite 3). These cells normally provide only non-neuronal cells to the nodose ganglion, but produce neurons in other regions. At day 9, quail-derived neurons were identified in the right nodose ganglia of these chimeras, indicating that cardiac neural crest cells can generate neurons in the ganglion when placode-derived neurons are absent or reduced in number. On the other hand, we found that "sympathetic" neural crest (from somites 10 to 20) does not support ganglion development, suggesting that only neural crest cells normally present in the ganglion participate in reconstituting its neuronal population. Our previous work has shown that right nodose placode ablation produces abnormal cardiac function, which mimics a life-threatening human heart condition known as long QT syndrome. The present results suggest that the presence of neural crest-derived neurons in the developing right nodose ganglion may contribute to the functional abnormality in long QT syndrome.

摘要

结状神经节是迷走神经的远侧颅神经节,为心脏和其他内脏提供感觉神经支配。在本研究中,通过切除第9期鸡胚的右侧结状基板,实现了去除正常填充右侧结状神经节的神经元前体。随后的组织学评估显示,在存活至第6天的受损胚胎中,54%没有右侧神经节。然而,大多数存活至第12天的胚胎有可识别的右侧神经节。在第12天的胚胎中,发育的右侧神经节异常,与对照神经节相比,神经节体积和神经节细胞直径分别减少了50%和20%。为了研究再生神经节中神经元群体的来源,我们将结状基板切除与用鹌鹑“心脏”神经嵴(从中耳基板到体节3)双侧替代鸡胚相结合。这些细胞通常只为结状神经节提供非神经元细胞,但在其他区域产生神经元。在第9天,在这些嵌合体的右侧结状神经节中鉴定出鹌鹑来源的神经元,表明当基板来源的神经元缺失或数量减少时,心脏神经嵴细胞可以在神经节中产生神经元。另一方面,我们发现“交感”神经嵴(从体节10到20)不支持神经节发育,这表明只有神经节中正常存在的神经嵴细胞参与其神经元群体的重建。我们之前的工作表明,右侧结状基板切除会导致心脏功能异常,这类似于一种危及生命的人类心脏疾病——长QT综合征。目前的结果表明,发育中的右侧结状神经节中神经嵴来源的神经元的存在可能导致长QT综合征的功能异常。

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