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来自白令海的深海柱头虫Quatuoralisia malakhovi(半索动物门,肠鳃纲,Torquaratoridae科)的雄性生殖系统。

Male reproductive system of the deep-sea acorn worm Quatuoralisia malakhovi (Hemichordata, Enteropneusta, Torquaratoridae) from the Bering Sea.

作者信息

Lukinykh Anastasiya Ivanovna, Ezhova Olga Vladimirovna, Yushin Vladimir Vladimirovich, Galkin Sergey Vladimirovich, Malakhov Vladimir Vasilievich

机构信息

Biological Faculty, Department of Invertebrate Zoology, Lomonosov Moscow State University, Leninskie Gory, 1, Bld. 12, Moscow, Russia, 119234.

A.V. Zhirmunsky National Scientific Center of Marine Biology, Far Eastern Branch, Russian Academy of Sciences (NSCMB FEB RAS), Palchevskogo Str. 17, Vladivostok, Russia, 690041.

出版信息

Front Zool. 2024 Oct 8;21(1):26. doi: 10.1186/s12983-024-00548-w.

DOI:10.1186/s12983-024-00548-w
PMID:39379961
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11459992/
Abstract

BACKGROUND

The deep-sea acorn worm Quatuoralisia malakhovi belongs to the phylum Hemichordata, class Enteropneusta, family Torquaratoridae, which was described in 2005. Owing to their epibenthic lifestyle and deep-sea habitat features, torquaratorids differ anatomically from shallow-water acorn worms; however, their morphology and fine structure are poorly studied. We have the opportunity to make three complete detailed series of histological sections of Q. malakhovi and to study the microscopic anatomy, histology and fine structure of the reproductive system of this acorn worm using scanning and transmission electron microscopy.

RESULTS

The sexes of Q. malakhovi are separate and indistinguishable externally. The lobed testes occupy the dorsal side of the genital wings and distinctly bulge into the peribranchial cavity by their mature lobes. The central part of the testis is always submerged into the genital wing and opens via a single gonad pore. The monociliary muscle cells stretch along the external wall of the testis and surround the gonad pore, probably taking part in the contraction of the testis lobes for spawning. The germinative epithelium of the testis contains spermatogenic cells at different stages of development and interstitial cells. Yolk cells are not found. Interstitial cells embrace the spermatogonia and spermatogenic columns, providing horizontal compartmentalization of the germinative epithelium, and contain numerous phagosomes with remnants of degenerating spermatogenic cells. The testis wall contains haemal lacunae, which are usually located on the side opposite the gonad pore. We describe the fine structure of spermatogonia, spermatocytes clustered in spermatogenic columns, spermatids, and spermatozoa. Spermatozoa are of the ectaquasperm type and consist of an acorn-shaped head and a flagellum 18-25 µm long. The sperm head includes a beak-shaped acrosomal part, a spherical nucleus and a midpiece containing a ring of 5 or rarely 6 mitochondria.

CONCLUSIONS

The male reproductive system and sperm structure of Q. malakhovi, a representative of the family Torquaratoridae, have a number of differences from shallow-water acorn worms; however, the spermatogenesis and sperm structure of Q. malakhovi generally follow the pattern of the other three enteropneust families, and the phylogenetic significance of these deviations should be the subject of further research.

摘要

背景

深海橡实虫马氏四鳃虫属于半索动物门、肠鳃纲、扭鳃虫科,于2005年被描述。由于其底栖生物的生活方式和深海栖息地特征,扭鳃虫科在解剖学上与浅水橡实虫不同;然而,它们的形态和精细结构研究较少。我们有机会制作了马氏四鳃虫的三个完整详细的组织学切片系列,并使用扫描电子显微镜和透射电子显微镜研究了这种橡实虫生殖系统的微观解剖结构、组织学和精细结构。

结果

马氏四鳃虫雌雄异体,外部无法区分。叶状睾丸占据生殖翼的背侧,成熟叶明显突入鳃周腔。睾丸的中央部分始终浸没在生殖翼中,并通过单个生殖孔开口。单纤毛肌细胞沿着睾丸外壁伸展并围绕生殖孔,可能参与睾丸叶的收缩以进行产卵。睾丸的生发上皮包含处于不同发育阶段的生精细胞和间质细胞。未发现卵黄细胞。间质细胞包围精原细胞和生精柱,为生发上皮提供水平分隔,并含有许多带有退化生精细胞残余物的吞噬体。睾丸壁含有血腔隙,通常位于与生殖孔相对的一侧。我们描述了精原细胞、聚集在生精柱中的精母细胞、精子细胞和精子的精细结构。精子属于外鞭毛精子类型,由橡子形头部和长18 - 25微米的鞭毛组成。精子头部包括喙形顶体部分、球形细胞核和含有5个或很少6个线粒体环的中段。

结论

扭鳃虫科的代表物种马氏四鳃虫的雄性生殖系统和精子结构与浅水橡实虫有许多不同;然而,马氏四鳃虫的精子发生和精子结构总体上遵循其他三个肠鳃科的模式,这些差异的系统发育意义应是进一步研究的主题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66c8/11459992/b100d4429f87/12983_2024_548_Fig13_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66c8/11459992/92c0f9d533e5/12983_2024_548_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66c8/11459992/b91545f7f59b/12983_2024_548_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66c8/11459992/825652a467dd/12983_2024_548_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66c8/11459992/dce8831734eb/12983_2024_548_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66c8/11459992/9a9f90409d35/12983_2024_548_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66c8/11459992/41dfc4c63191/12983_2024_548_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66c8/11459992/fd0f2d9a6c89/12983_2024_548_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66c8/11459992/14f9ef4ff25a/12983_2024_548_Fig11_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66c8/11459992/06d52ce367bb/12983_2024_548_Fig12_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66c8/11459992/b100d4429f87/12983_2024_548_Fig13_HTML.jpg

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