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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 hav...

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Autores principales: Durkina, Valentina B., Chapman, John W., Demchenko, Natalia L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8918206/
https://www.ncbi.nlm.nih.gov/pubmed/35291485
http://dx.doi.org/10.7717/peerj.12950
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author Durkina, Valentina B.
Chapman, John W.
Demchenko, Natalia L.
author_facet Durkina, Valentina B.
Chapman, John W.
Demchenko, Natalia L.
author_sort Durkina, Valentina B.
collection PubMed
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 ovaries to reproduce a second brood. The precursors of these third-year females (a small number the second-year females with an asynchronous [summer] breeding period and ovaries that have atrophied due to seasonal starvation) appear to possess sources of somatic and germ cells that are sufficient for ovarian regeneration and that may be adaptations to starvation stress.
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spelling pubmed-89182062022-03-14 First observations of ovary regeneration in an amphipod, Ampelisca eschrichtii Krøyer, 1842 Durkina, Valentina B. Chapman, John W. Demchenko, Natalia L. PeerJ Conservation Biology 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 ovaries to reproduce a second brood. The precursors of these third-year females (a small number the second-year females with an asynchronous [summer] breeding period and ovaries that have atrophied due to seasonal starvation) appear to possess sources of somatic and germ cells that are sufficient for ovarian regeneration and that may be adaptations to starvation stress. PeerJ Inc. 2022-03-10 /pmc/articles/PMC8918206/ /pubmed/35291485 http://dx.doi.org/10.7717/peerj.12950 Text en © 2022 Durkina et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Conservation Biology
Durkina, Valentina B.
Chapman, John W.
Demchenko, Natalia L.
First observations of ovary regeneration in an amphipod, Ampelisca eschrichtii Krøyer, 1842
title 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_short 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
topic Conservation Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8918206/
https://www.ncbi.nlm.nih.gov/pubmed/35291485
http://dx.doi.org/10.7717/peerj.12950
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