First observations of ovary regeneration in an amphipod, Ampelisca eschrichtii Krøyer, 1842

Background Females of the gammaridean amphipod Ampelisca eschrichtii with signs of regenerating, previously atrophied ovaries were recovered from the northeastern shelf of Sakhalin Island (Okhotsk Sea, Russia). Ovarian regeneration was previously unknown for any amphipod species. A. eschrichtii have...

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Published in:PeerJ
Main Authors: Valentina B. Durkina, John W. Chapman, Natalia L. Demchenko
Format: Article in Journal/Newspaper
Language:English
Published: PeerJ Inc. 2022
Subjects:
R
Online Access:https://doi.org/10.7717/peerj.12950
https://doaj.org/article/bf76ab604d2b45b698bc6d80f7d090b1
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spelling ftdoajarticles:oai:doaj.org/article:bf76ab604d2b45b698bc6d80f7d090b1 2024-01-07T09:45:47+01:00 First observations of ovary regeneration in an amphipod, Ampelisca eschrichtii Krøyer, 1842 Valentina B. Durkina John W. Chapman Natalia L. Demchenko 2022-03-01T00:00:00Z https://doi.org/10.7717/peerj.12950 https://doaj.org/article/bf76ab604d2b45b698bc6d80f7d090b1 EN eng PeerJ Inc. https://peerj.com/articles/12950.pdf https://peerj.com/articles/12950/ https://doaj.org/toc/2167-8359 doi:10.7717/peerj.12950 2167-8359 https://doaj.org/article/bf76ab604d2b45b698bc6d80f7d090b1 PeerJ, Vol 10, p e12950 (2022) Amphipoda Histology Okhotsk Sea Germ cells Eosinophilic cells Reproduction Medicine R Biology (General) QH301-705.5 article 2022 ftdoajarticles https://doi.org/10.7717/peerj.12950 2023-12-10T01:52:21Z Background Females of the gammaridean amphipod Ampelisca eschrichtii with signs of regenerating, previously atrophied ovaries were recovered from the northeastern shelf of Sakhalin Island (Okhotsk Sea, Russia). Ovarian regeneration was previously unknown for any amphipod species. A. eschrichtii have a predominantly 2-year life cycle (from embryo to adult death) and reproduce once between late winter or early spring at the age of 2 years. Occasionally, females survive to a third year. An adaptive value of extended survival among these females is likely to require that they are also reproductive. Methods Histological sections from a second-year female with ovarian atrophy, a female with normal ovaries, a third-year female with ovarian regeneration, as well as testes of an immature and a sexually mature male were compared to determine the sources of cells of the germinal and somatic lines necessary for ovarian regeneration. Results Ovarian regeneration in the third-year female began with the formation of a new germinal zone from germ cells preserved in the atrophied ovaries and eosinophilic cells of the previously starving second-year female. Eosinophilic cells form the mesodermal component of the germinal zone. A mass of these cells appeared in the second-year female that had atrophied ovaries and in large numbers on the intestine wall of the third-year female with regenerating ovaries. These eosinophilic cells appear to migrate into the regenerating ovaries. Conclusions All germ cells of the second-year female are not lost during ovarian atrophy and can be involved in subsequent ovarian regeneration. Eosinophilic cells involved in ovarian regeneration are of mesodermal origin. The eosinophilic cell morphologies are similar to those of quiescence cells (cells in a reversible state that do not divide but retain the ability to re-enter cell division and participate in regeneration). These histological data thus indicate that eosinophilic and germ cells of third-year females can participate in the regeneration of the ... Article in Journal/Newspaper okhotsk sea Sakhalin Directory of Open Access Journals: DOAJ Articles Okhotsk PeerJ 10 e12950
institution Open Polar
collection Directory of Open Access Journals: DOAJ Articles
op_collection_id ftdoajarticles
language English
topic Amphipoda
Histology
Okhotsk Sea
Germ cells
Eosinophilic cells
Reproduction
Medicine
R
Biology (General)
QH301-705.5
spellingShingle Amphipoda
Histology
Okhotsk Sea
Germ cells
Eosinophilic cells
Reproduction
Medicine
R
Biology (General)
QH301-705.5
Valentina B. Durkina
John W. Chapman
Natalia L. Demchenko
First observations of ovary regeneration in an amphipod, Ampelisca eschrichtii Krøyer, 1842
topic_facet Amphipoda
Histology
Okhotsk Sea
Germ cells
Eosinophilic cells
Reproduction
Medicine
R
Biology (General)
QH301-705.5
description Background Females of the gammaridean amphipod Ampelisca eschrichtii with signs of regenerating, previously atrophied ovaries were recovered from the northeastern shelf of Sakhalin Island (Okhotsk Sea, Russia). Ovarian regeneration was previously unknown for any amphipod species. A. eschrichtii have a predominantly 2-year life cycle (from embryo to adult death) and reproduce once between late winter or early spring at the age of 2 years. Occasionally, females survive to a third year. An adaptive value of extended survival among these females is likely to require that they are also reproductive. Methods Histological sections from a second-year female with ovarian atrophy, a female with normal ovaries, a third-year female with ovarian regeneration, as well as testes of an immature and a sexually mature male were compared to determine the sources of cells of the germinal and somatic lines necessary for ovarian regeneration. Results Ovarian regeneration in the third-year female began with the formation of a new germinal zone from germ cells preserved in the atrophied ovaries and eosinophilic cells of the previously starving second-year female. Eosinophilic cells form the mesodermal component of the germinal zone. A mass of these cells appeared in the second-year female that had atrophied ovaries and in large numbers on the intestine wall of the third-year female with regenerating ovaries. These eosinophilic cells appear to migrate into the regenerating ovaries. Conclusions All germ cells of the second-year female are not lost during ovarian atrophy and can be involved in subsequent ovarian regeneration. Eosinophilic cells involved in ovarian regeneration are of mesodermal origin. The eosinophilic cell morphologies are similar to those of quiescence cells (cells in a reversible state that do not divide but retain the ability to re-enter cell division and participate in regeneration). These histological data thus indicate that eosinophilic and germ cells of third-year females can participate in the regeneration of the ...
format Article in Journal/Newspaper
author Valentina B. Durkina
John W. Chapman
Natalia L. Demchenko
author_facet Valentina B. Durkina
John W. Chapman
Natalia L. Demchenko
author_sort Valentina B. Durkina
title First observations of ovary regeneration in an amphipod, Ampelisca eschrichtii Krøyer, 1842
title_short First observations of ovary regeneration in an amphipod, Ampelisca eschrichtii Krøyer, 1842
title_full First observations of ovary regeneration in an amphipod, Ampelisca eschrichtii Krøyer, 1842
title_fullStr First observations of ovary regeneration in an amphipod, Ampelisca eschrichtii Krøyer, 1842
title_full_unstemmed First observations of ovary regeneration in an amphipod, Ampelisca eschrichtii Krøyer, 1842
title_sort first observations of ovary regeneration in an amphipod, ampelisca eschrichtii krøyer, 1842
publisher PeerJ Inc.
publishDate 2022
url https://doi.org/10.7717/peerj.12950
https://doaj.org/article/bf76ab604d2b45b698bc6d80f7d090b1
geographic Okhotsk
geographic_facet Okhotsk
genre okhotsk sea
Sakhalin
genre_facet okhotsk sea
Sakhalin
op_source PeerJ, Vol 10, p e12950 (2022)
op_relation https://peerj.com/articles/12950.pdf
https://peerj.com/articles/12950/
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doi:10.7717/peerj.12950
2167-8359
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