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A meiotic switch in lysosome activity supports spermatocyte development in young flies but collapses with age

Gamete development ultimately influences animal fertility. Identifying mechanisms that direct gametogenesis, and how they deteriorate with age, may inform ways to combat infertility. Recently, we found that lysosomes acidify during oocyte maturation in Caenorhabditis elegans, suggesting that a meiot...

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Detalles Bibliográficos
Autores principales: Butsch, Tyler J., Dubuisson, Olga, Johnson, Alyssa E., Bohnert, K. Adam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9126793/
https://www.ncbi.nlm.nih.gov/pubmed/35620438
http://dx.doi.org/10.1016/j.isci.2022.104382
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author Butsch, Tyler J.
Dubuisson, Olga
Johnson, Alyssa E.
Bohnert, K. Adam
author_facet Butsch, Tyler J.
Dubuisson, Olga
Johnson, Alyssa E.
Bohnert, K. Adam
author_sort Butsch, Tyler J.
collection PubMed
description Gamete development ultimately influences animal fertility. Identifying mechanisms that direct gametogenesis, and how they deteriorate with age, may inform ways to combat infertility. Recently, we found that lysosomes acidify during oocyte maturation in Caenorhabditis elegans, suggesting that a meiotic switch in lysosome activity promotes female germ-cell health. Using Drosophila melanogaster, we report that lysosomes likewise acidify in male germ cells during meiosis. Inhibiting lysosomes in young-male testes causes E-cadherin accumulation and loss of germ-cell partitioning membranes. Notably, analogous changes occur naturally during aging; in older testes, a reduction in lysosome acidity precedes E-cadherin accumulation and membrane dissolution, suggesting one potential cause of age-related spermatocyte abnormalities. Consistent with lysosomes governing the production of mature sperm, germ cells with homozygous-null mutations in lysosome-acidifying machinery fail to survive through meiosis. Thus, lysosome activation is entrained to meiotic progression in developing sperm, as in oocytes, and lysosomal dysfunction may instigate male reproductive aging.
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spelling pubmed-91267932022-05-25 A meiotic switch in lysosome activity supports spermatocyte development in young flies but collapses with age Butsch, Tyler J. Dubuisson, Olga Johnson, Alyssa E. Bohnert, K. Adam iScience Article Gamete development ultimately influences animal fertility. Identifying mechanisms that direct gametogenesis, and how they deteriorate with age, may inform ways to combat infertility. Recently, we found that lysosomes acidify during oocyte maturation in Caenorhabditis elegans, suggesting that a meiotic switch in lysosome activity promotes female germ-cell health. Using Drosophila melanogaster, we report that lysosomes likewise acidify in male germ cells during meiosis. Inhibiting lysosomes in young-male testes causes E-cadherin accumulation and loss of germ-cell partitioning membranes. Notably, analogous changes occur naturally during aging; in older testes, a reduction in lysosome acidity precedes E-cadherin accumulation and membrane dissolution, suggesting one potential cause of age-related spermatocyte abnormalities. Consistent with lysosomes governing the production of mature sperm, germ cells with homozygous-null mutations in lysosome-acidifying machinery fail to survive through meiosis. Thus, lysosome activation is entrained to meiotic progression in developing sperm, as in oocytes, and lysosomal dysfunction may instigate male reproductive aging. Elsevier 2022-05-10 /pmc/articles/PMC9126793/ /pubmed/35620438 http://dx.doi.org/10.1016/j.isci.2022.104382 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Butsch, Tyler J.
Dubuisson, Olga
Johnson, Alyssa E.
Bohnert, K. Adam
A meiotic switch in lysosome activity supports spermatocyte development in young flies but collapses with age
title A meiotic switch in lysosome activity supports spermatocyte development in young flies but collapses with age
title_full A meiotic switch in lysosome activity supports spermatocyte development in young flies but collapses with age
title_fullStr A meiotic switch in lysosome activity supports spermatocyte development in young flies but collapses with age
title_full_unstemmed A meiotic switch in lysosome activity supports spermatocyte development in young flies but collapses with age
title_short A meiotic switch in lysosome activity supports spermatocyte development in young flies but collapses with age
title_sort meiotic switch in lysosome activity supports spermatocyte development in young flies but collapses with age
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9126793/
https://www.ncbi.nlm.nih.gov/pubmed/35620438
http://dx.doi.org/10.1016/j.isci.2022.104382
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