Sthenelanella(环节动物:sigalionae科)的上层“纺丝腺”是经过修饰的毛囊

IF 1.3 4区 生物学 Q3 MARINE & FRESHWATER BIOLOGY
Ekin Tilic, Alicia Geratz, Greg W. Rouse, Thomas Bartolomaeus
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引用次数: 3

摘要

摘要Sthenelanella是一种不寻常的管栖鳞虫属,身体两侧都有细小的纤维丝状结构。这些纤维以长长的银色束的形式出现在背部,然后紧密地交织在一起,形成了毛毡状的管状材料。在文献中,这些纤维被描述为所谓的“纺丝腺”的产物。本文研究了这些非拓扑纤维的超微结构,表明它们是环节动物毛纲。每一种毛毛由基部的毛质母细胞的三到四个动态微绒毛构成,使它们成为已知最薄的环节动物刚毛。我们的研究结果表明,均匀Sthenelanella的纺丝腺是额外的,高度修饰的非拓扑毛囊。我们还表明,卵泡细胞通过分泌牙釉质层,在最终毛囊的形成中起着积极的作用。这些发现不仅增加了已知的毛纲形态多样性,而且还证明了形成这些几丁质结构的机制的明显可塑性。我们的研究结果与其他环节动物中的毛羽进行了比较,特别关注了拟龙目中类似的纤维状毛羽。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Notopodial “spinning glands” of Sthenelanella (Annelida: Sigalionidae) are modified chaetal sacs

Notopodial “spinning glands” of Sthenelanella (Annelida: Sigalionidae) are modified chaetal sacs

Sthenelanella is an unusual genus of tube-dwelling scale worms, with fine fibrous threads that appear on either side of the body. These fibers emerge dorsally in long silvery bundles that are then tightly interwoven to construct the felt-like material of the tube. In the literature, these fibers are described as the products of so-called “spinning glands.” In this article, we investigated the ultrastructure of these notopodial fibers and show that they are annelid chaetae. Three or four dynamic microvilli of a basal chaetoblast form each of these feltage chaetae, making them the thinnest known annelid bristles. Our results show that the spinning glands of Sthenelanella uniformis are additional, highly modified notopodial chaetal sacs. We also show that the follicle cells, by their secretion of the enamel layer, play an active role in shaping the final chaeta. These findings not only increase the known morphological diversity of chaetae but also demonstrate the apparent plasticity of the machinery that form these chitinous structures. Our results are compared with chaetae in other annelids, with a particular focus on similar fibrous chaetae in Aphroditiformia.

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来源期刊
Invertebrate Biology
Invertebrate Biology 生物-动物学
CiteScore
2.20
自引率
8.30%
发文量
28
审稿时长
>12 weeks
期刊介绍: Invertebrate Biology presents fundamental advances in our understanding of the structure, function, ecology, and evolution of the invertebrates, which represent the vast majority of animal diversity. Though ultimately organismal in focus, the journal publishes manuscripts addressing phenomena at all levels of biological organization. Invertebrate Biology welcomes manuscripts addressing the biology of invertebrates from diverse perspectives, including those of: • genetics, cell, and molecular biology • morphology and biomechanics • reproduction and development • physiology and behavior • ecology • evolution and phylogenetics
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