The Rohde-like cells at the posterior end of the dorsal nerve cord of amphioxus (Cephalochordata)

IF 2.3 4区 医学 Q3 NEUROSCIENCES
Nicholas D. Holland, Linda Z. Holland
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Abstract

For postmetamorphic specimens of amphioxus (Cephalochordata), serial block-face scanning electron microscopy (SBSEM) is used to describe the long-ignored Rohde-like cells (RLCs) at the extreme posterior end of the dorsal nerve cord. These cells, numbering about three dozen in all, are divisible into a group with larger diameters running near the dorsal side of the cord and a more ventral group with smaller diameters closely associated with the central canal of the neurocoel. It is possible that the smaller ventral cells might be generated at the ependymal zone of the dorsal nerve cord and later migrate to a dorsal position, although a functional reason for this remains a mystery. All the RLCs have conspicuous regions of microvilli covering as much as 40% of their surface; limited data (by others) on the more anterior bona fide Rohde cells also indicate an extensive microvillar surface. Thus, both the RLCs and the better-known Rohde cells appear to be rhabdomeric photoreceptors, although a specific function for this feature is currently unknown. Even more perplexingly, although the Rohde cells are quintessential neurons extending giant processes, each RLC comprises a perikaryon that does not bear any neurites.

Abstract Image

文昌鱼(头足类)背神经索后部的类罗氏细胞。
对于文昌鱼(头脊柱动物门)的后变型标本,序列块面扫描电子显微镜(SBSEM)被用来描述背神经索极后端长期被忽视的罗德样细胞(RLCs)。这些细胞共有三十几个,可分为靠近脊髓背侧的直径较大的细胞群和与神经脊髓中央管密切相关的直径较小的腹侧细胞群。较小的腹侧细胞可能产生于背侧神经索的外膜区,后来迁移到背侧位置,但其功能原因仍是一个谜。所有的RLC都有明显的微绒毛区域,覆盖其表面的40%之多;关于更前端的真正Rohde细胞的有限数据(由其他人提供)也表明其表面有广泛的微绒毛。因此,RLCs 和更著名的 Rohde 细胞似乎都是横纹肌光感受器,尽管这一特征的具体功能目前尚不清楚。更令人费解的是,虽然罗德细胞是典型的神经元,延伸出巨大的突起,但每个 RLC 都由一个不带任何神经元的周核组成。
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来源期刊
CiteScore
5.80
自引率
8.00%
发文量
158
审稿时长
3-6 weeks
期刊介绍: Established in 1891, JCN is the oldest continually published basic neuroscience journal. Historically, as the name suggests, the journal focused on a comparison among species to uncover the intricacies of how the brain functions. In modern times, this research is called systems neuroscience where animal models are used to mimic core cognitive processes with the ultimate goal of understanding neural circuits and connections that give rise to behavioral patterns and different neural states. Research published in JCN covers all species from invertebrates to humans, and the reports inform the readers about the function and organization of nervous systems in species with an emphasis on the way that species adaptations inform about the function or organization of the nervous systems, rather than on their evolution per se. JCN publishes primary research articles and critical commentaries and review-type articles offering expert insight in to cutting edge research in the field of systems neuroscience; a complete list of contribution types is given in the Author Guidelines. For primary research contributions, only full-length investigative reports are desired; the journal does not accept short communications.
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