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Fibroblast growth factor 21 prolongs lifespan and improves stress tolerance in the silkworm, Bombyx mori
BACKGROUND: Fibroblast growth factor 21 (FGF21), an FGF family member, is an atypical hormone and pro-longevity factor. METHODS: To better understand of the effects of exogenous administration of FGF21 on lifespan and stress tolerance, and the underlying molecular basis, we used the silkworm, Bombyx...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7154471/ https://www.ncbi.nlm.nih.gov/pubmed/32309367 http://dx.doi.org/10.21037/atm.2020.01.18 |
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author | Song, Jiang-Bo Hao, Kai-Ge Chen, Xin Zhang, Yan-Hua Cheng, Zi-Lin Mao, Shuang Tang, Yong-Xi Tong, Xiao-Ling Dai, Fang-Yin |
author_facet | Song, Jiang-Bo Hao, Kai-Ge Chen, Xin Zhang, Yan-Hua Cheng, Zi-Lin Mao, Shuang Tang, Yong-Xi Tong, Xiao-Ling Dai, Fang-Yin |
author_sort | Song, Jiang-Bo |
collection | PubMed |
description | BACKGROUND: Fibroblast growth factor 21 (FGF21), an FGF family member, is an atypical hormone and pro-longevity factor. METHODS: To better understand of the effects of exogenous administration of FGF21 on lifespan and stress tolerance, and the underlying molecular basis, we used the silkworm, Bombyx mori, as an experimental animal model to evaluate FGF21’s pharmaceutical effects. RESULTS: Lifespan was significantly prolonged in female silkworms with FGF21 replenishment, whereas no effect was observed in the male silkworms. FGF21 replenishment also significantly improved the activity of antioxidant systems such as glutathione-S-transferase (GST) and superoxide dismutase (SOD) and significantly decreased malondialdehyde (MDA) content. Moreover, FGF21 was found to play a critical role in enhancing stress resistance, including ultraviolet (UV) irradiation tolerance and thermotolerance. Furthermore, AMPK, FoxO, and sirtuins were activated by FGF21 and may be responsible for the prolonged lifespan and enhanced antioxidant activity observed in silkworms. CONCLUSIONS: Collectively, the results suggest the molecular pathways underlying of FGF21-induced longevity and stress tolerance, and support the use of silkworms as a promising experimental animal model for evaluating the pharmaceutical effects of small molecules. |
format | Online Article Text |
id | pubmed-7154471 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-71544712020-04-17 Fibroblast growth factor 21 prolongs lifespan and improves stress tolerance in the silkworm, Bombyx mori Song, Jiang-Bo Hao, Kai-Ge Chen, Xin Zhang, Yan-Hua Cheng, Zi-Lin Mao, Shuang Tang, Yong-Xi Tong, Xiao-Ling Dai, Fang-Yin Ann Transl Med Original Article BACKGROUND: Fibroblast growth factor 21 (FGF21), an FGF family member, is an atypical hormone and pro-longevity factor. METHODS: To better understand of the effects of exogenous administration of FGF21 on lifespan and stress tolerance, and the underlying molecular basis, we used the silkworm, Bombyx mori, as an experimental animal model to evaluate FGF21’s pharmaceutical effects. RESULTS: Lifespan was significantly prolonged in female silkworms with FGF21 replenishment, whereas no effect was observed in the male silkworms. FGF21 replenishment also significantly improved the activity of antioxidant systems such as glutathione-S-transferase (GST) and superoxide dismutase (SOD) and significantly decreased malondialdehyde (MDA) content. Moreover, FGF21 was found to play a critical role in enhancing stress resistance, including ultraviolet (UV) irradiation tolerance and thermotolerance. Furthermore, AMPK, FoxO, and sirtuins were activated by FGF21 and may be responsible for the prolonged lifespan and enhanced antioxidant activity observed in silkworms. CONCLUSIONS: Collectively, the results suggest the molecular pathways underlying of FGF21-induced longevity and stress tolerance, and support the use of silkworms as a promising experimental animal model for evaluating the pharmaceutical effects of small molecules. AME Publishing Company 2020-03 /pmc/articles/PMC7154471/ /pubmed/32309367 http://dx.doi.org/10.21037/atm.2020.01.18 Text en 2020 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Original Article Song, Jiang-Bo Hao, Kai-Ge Chen, Xin Zhang, Yan-Hua Cheng, Zi-Lin Mao, Shuang Tang, Yong-Xi Tong, Xiao-Ling Dai, Fang-Yin Fibroblast growth factor 21 prolongs lifespan and improves stress tolerance in the silkworm, Bombyx mori |
title | Fibroblast growth factor 21 prolongs lifespan and improves stress tolerance in the silkworm, Bombyx mori |
title_full | Fibroblast growth factor 21 prolongs lifespan and improves stress tolerance in the silkworm, Bombyx mori |
title_fullStr | Fibroblast growth factor 21 prolongs lifespan and improves stress tolerance in the silkworm, Bombyx mori |
title_full_unstemmed | Fibroblast growth factor 21 prolongs lifespan and improves stress tolerance in the silkworm, Bombyx mori |
title_short | Fibroblast growth factor 21 prolongs lifespan and improves stress tolerance in the silkworm, Bombyx mori |
title_sort | fibroblast growth factor 21 prolongs lifespan and improves stress tolerance in the silkworm, bombyx mori |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7154471/ https://www.ncbi.nlm.nih.gov/pubmed/32309367 http://dx.doi.org/10.21037/atm.2020.01.18 |
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