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Social reprogramming in ants induces longevity-associated glia remodeling
In social insects, workers and queens arise from the same genome but display profound differences in behavior and longevity. In Harpegnathos saltator ants, adult workers can transition to a queen-like state called gamergate, which results in reprogramming of social behavior and life-span extension....
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7438095/ https://www.ncbi.nlm.nih.gov/pubmed/32875108 http://dx.doi.org/10.1126/sciadv.aba9869 |
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author | Sheng, Lihong Shields, Emily J. Gospocic, Janko Glastad, Karl M. Ratchasanmuang, Puttachai Berger, Shelley L. Raj, Arjun Little, Shawn Bonasio, Roberto |
author_facet | Sheng, Lihong Shields, Emily J. Gospocic, Janko Glastad, Karl M. Ratchasanmuang, Puttachai Berger, Shelley L. Raj, Arjun Little, Shawn Bonasio, Roberto |
author_sort | Sheng, Lihong |
collection | PubMed |
description | In social insects, workers and queens arise from the same genome but display profound differences in behavior and longevity. In Harpegnathos saltator ants, adult workers can transition to a queen-like state called gamergate, which results in reprogramming of social behavior and life-span extension. Using single-cell RNA sequencing, we compared the distribution of neuronal and glial populations before and after the social transition. We found that the conversion of workers into gamergates resulted in the expansion of neuroprotective ensheathing glia. Brain injury assays revealed that activation of the damage response gene Mmp1 was weaker in old workers, where the relative frequency of ensheathing glia also declined. On the other hand, long-lived gamergates retained a larger fraction of ensheathing glia and the ability to mount a strong Mmp1 response to brain injury into old age. We also observed molecular and cellular changes suggestive of age-associated decline in ensheathing glia in Drosophila. |
format | Online Article Text |
id | pubmed-7438095 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-74380952020-08-31 Social reprogramming in ants induces longevity-associated glia remodeling Sheng, Lihong Shields, Emily J. Gospocic, Janko Glastad, Karl M. Ratchasanmuang, Puttachai Berger, Shelley L. Raj, Arjun Little, Shawn Bonasio, Roberto Sci Adv Research Articles In social insects, workers and queens arise from the same genome but display profound differences in behavior and longevity. In Harpegnathos saltator ants, adult workers can transition to a queen-like state called gamergate, which results in reprogramming of social behavior and life-span extension. Using single-cell RNA sequencing, we compared the distribution of neuronal and glial populations before and after the social transition. We found that the conversion of workers into gamergates resulted in the expansion of neuroprotective ensheathing glia. Brain injury assays revealed that activation of the damage response gene Mmp1 was weaker in old workers, where the relative frequency of ensheathing glia also declined. On the other hand, long-lived gamergates retained a larger fraction of ensheathing glia and the ability to mount a strong Mmp1 response to brain injury into old age. We also observed molecular and cellular changes suggestive of age-associated decline in ensheathing glia in Drosophila. American Association for the Advancement of Science 2020-08-19 /pmc/articles/PMC7438095/ /pubmed/32875108 http://dx.doi.org/10.1126/sciadv.aba9869 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Sheng, Lihong Shields, Emily J. Gospocic, Janko Glastad, Karl M. Ratchasanmuang, Puttachai Berger, Shelley L. Raj, Arjun Little, Shawn Bonasio, Roberto Social reprogramming in ants induces longevity-associated glia remodeling |
title | Social reprogramming in ants induces longevity-associated glia remodeling |
title_full | Social reprogramming in ants induces longevity-associated glia remodeling |
title_fullStr | Social reprogramming in ants induces longevity-associated glia remodeling |
title_full_unstemmed | Social reprogramming in ants induces longevity-associated glia remodeling |
title_short | Social reprogramming in ants induces longevity-associated glia remodeling |
title_sort | social reprogramming in ants induces longevity-associated glia remodeling |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7438095/ https://www.ncbi.nlm.nih.gov/pubmed/32875108 http://dx.doi.org/10.1126/sciadv.aba9869 |
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