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Age-related mushroom body expansion in male sweat bees and bumble bees
A well-documented phenomenon among social insects is that brain changes occur prior to or at the onset of certain experiences, potentially serving to prime the brain for specific tasks. This insight comes almost exclusively from studies considering developmental maturation in females. As a result, i...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8382693/ https://www.ncbi.nlm.nih.gov/pubmed/34426595 http://dx.doi.org/10.1038/s41598-021-96268-w |
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author | Hagadorn, Mallory A. Eck, Karlee Del Grosso, Matthew Haemmerle, Xavier Wcislo, William T. Kapheim, Karen M. |
author_facet | Hagadorn, Mallory A. Eck, Karlee Del Grosso, Matthew Haemmerle, Xavier Wcislo, William T. Kapheim, Karen M. |
author_sort | Hagadorn, Mallory A. |
collection | PubMed |
description | A well-documented phenomenon among social insects is that brain changes occur prior to or at the onset of certain experiences, potentially serving to prime the brain for specific tasks. This insight comes almost exclusively from studies considering developmental maturation in females. As a result, it is unclear whether age-related brain plasticity is consistent across sexes, and to what extent developmental patterns differ. Using confocal microscopy and volumetric analyses, we investigated age-related brain changes coinciding with sexual maturation in the males of the facultatively eusocial sweat bee, Megalopta genalis, and the obligately eusocial bumble bee, Bombus impatiens. We compared volumetric measurements between newly eclosed and reproductively mature males kept isolated in the lab. We found expansion of the mushroom bodies—brain regions associated with learning and memory—with maturation, which were consistent across both species. This age-related plasticity may, therefore, play a functionally-relevant role in preparing male bees for mating, and suggests that developmentally-driven neural restructuring can occur in males, even in species where it is absent in females. |
format | Online Article Text |
id | pubmed-8382693 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83826932021-09-01 Age-related mushroom body expansion in male sweat bees and bumble bees Hagadorn, Mallory A. Eck, Karlee Del Grosso, Matthew Haemmerle, Xavier Wcislo, William T. Kapheim, Karen M. Sci Rep Article A well-documented phenomenon among social insects is that brain changes occur prior to or at the onset of certain experiences, potentially serving to prime the brain for specific tasks. This insight comes almost exclusively from studies considering developmental maturation in females. As a result, it is unclear whether age-related brain plasticity is consistent across sexes, and to what extent developmental patterns differ. Using confocal microscopy and volumetric analyses, we investigated age-related brain changes coinciding with sexual maturation in the males of the facultatively eusocial sweat bee, Megalopta genalis, and the obligately eusocial bumble bee, Bombus impatiens. We compared volumetric measurements between newly eclosed and reproductively mature males kept isolated in the lab. We found expansion of the mushroom bodies—brain regions associated with learning and memory—with maturation, which were consistent across both species. This age-related plasticity may, therefore, play a functionally-relevant role in preparing male bees for mating, and suggests that developmentally-driven neural restructuring can occur in males, even in species where it is absent in females. Nature Publishing Group UK 2021-08-23 /pmc/articles/PMC8382693/ /pubmed/34426595 http://dx.doi.org/10.1038/s41598-021-96268-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Hagadorn, Mallory A. Eck, Karlee Del Grosso, Matthew Haemmerle, Xavier Wcislo, William T. Kapheim, Karen M. Age-related mushroom body expansion in male sweat bees and bumble bees |
title | Age-related mushroom body expansion in male sweat bees and bumble bees |
title_full | Age-related mushroom body expansion in male sweat bees and bumble bees |
title_fullStr | Age-related mushroom body expansion in male sweat bees and bumble bees |
title_full_unstemmed | Age-related mushroom body expansion in male sweat bees and bumble bees |
title_short | Age-related mushroom body expansion in male sweat bees and bumble bees |
title_sort | age-related mushroom body expansion in male sweat bees and bumble bees |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8382693/ https://www.ncbi.nlm.nih.gov/pubmed/34426595 http://dx.doi.org/10.1038/s41598-021-96268-w |
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