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Fusion and expansion of vitellogenin vesicles during Caenorhabditis elegans intestinal senescence
Some of the most conspicuous aging phenotypes of C. elegans are related to post‐reproductive production of vitellogenins (Vtg), which form yolk protein (YP) complexes after processing and lipid loading. Vtg/YP levels show huge increases with age, and inhibition of this extends lifespan, but how subc...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9649609/ https://www.ncbi.nlm.nih.gov/pubmed/36199214 http://dx.doi.org/10.1111/acel.13719 |
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author | Zhai, Chao Zhang, Nan Li, Xi‐Xia Chen, Xi Sun, Fei Dong, Meng‐Qiu |
author_facet | Zhai, Chao Zhang, Nan Li, Xi‐Xia Chen, Xi Sun, Fei Dong, Meng‐Qiu |
author_sort | Zhai, Chao |
collection | PubMed |
description | Some of the most conspicuous aging phenotypes of C. elegans are related to post‐reproductive production of vitellogenins (Vtg), which form yolk protein (YP) complexes after processing and lipid loading. Vtg/YP levels show huge increases with age, and inhibition of this extends lifespan, but how subcellular and organism‐wide distribution of these proteins changes with age has not been systematically explored. Here, this has been done to understand how vitellogenesis promotes aging. The age‐associated changes of intestinal vitellogenin vesicles (VVs), pseudocoelomic yolk patches (PYPs), and gonadal yolk organelles (YOs) have been characterized by immuno‐electron microscopy. We find that from reproductive adult day 2 (AD 2) to post‐reproductive AD 6 and AD 9, intestinal VVs expand from 0.2 to 3–4 μm in diameter or by >3000 times in volume, PYPs increase by >3 times in YP concentration and volume, while YOs in oocytes shrink slightly from 0.5 to 0.4 μm in diameter or by 49% in volume. In AD 6 and AD 9 worms, mislocalized YOs found in the hypodermis, uterine cells, and the somatic gonadal sheath can reach a size of 10 μm across in the former two tissues. This remarkable size increase of VVs and that of mislocalized YOs in post‐reproductive worms are accompanied by extensive fusion between these Vtg/YP‐containing vesicular structures in somatic cells. In contrast, no fusion is seen between YOs in oocytes. We propose that in addition to the continued production of Vtg, excessive fusion between VVs and mislocalized YOs in the soma worsen the aging pathologies seen in C. elegans. |
format | Online Article Text |
id | pubmed-9649609 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96496092022-11-14 Fusion and expansion of vitellogenin vesicles during Caenorhabditis elegans intestinal senescence Zhai, Chao Zhang, Nan Li, Xi‐Xia Chen, Xi Sun, Fei Dong, Meng‐Qiu Aging Cell Research Articles Some of the most conspicuous aging phenotypes of C. elegans are related to post‐reproductive production of vitellogenins (Vtg), which form yolk protein (YP) complexes after processing and lipid loading. Vtg/YP levels show huge increases with age, and inhibition of this extends lifespan, but how subcellular and organism‐wide distribution of these proteins changes with age has not been systematically explored. Here, this has been done to understand how vitellogenesis promotes aging. The age‐associated changes of intestinal vitellogenin vesicles (VVs), pseudocoelomic yolk patches (PYPs), and gonadal yolk organelles (YOs) have been characterized by immuno‐electron microscopy. We find that from reproductive adult day 2 (AD 2) to post‐reproductive AD 6 and AD 9, intestinal VVs expand from 0.2 to 3–4 μm in diameter or by >3000 times in volume, PYPs increase by >3 times in YP concentration and volume, while YOs in oocytes shrink slightly from 0.5 to 0.4 μm in diameter or by 49% in volume. In AD 6 and AD 9 worms, mislocalized YOs found in the hypodermis, uterine cells, and the somatic gonadal sheath can reach a size of 10 μm across in the former two tissues. This remarkable size increase of VVs and that of mislocalized YOs in post‐reproductive worms are accompanied by extensive fusion between these Vtg/YP‐containing vesicular structures in somatic cells. In contrast, no fusion is seen between YOs in oocytes. We propose that in addition to the continued production of Vtg, excessive fusion between VVs and mislocalized YOs in the soma worsen the aging pathologies seen in C. elegans. John Wiley and Sons Inc. 2022-10-05 2022-11 /pmc/articles/PMC9649609/ /pubmed/36199214 http://dx.doi.org/10.1111/acel.13719 Text en © 2022 The Authors. Aging Cell published by Anatomical Society and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Zhai, Chao Zhang, Nan Li, Xi‐Xia Chen, Xi Sun, Fei Dong, Meng‐Qiu Fusion and expansion of vitellogenin vesicles during Caenorhabditis elegans intestinal senescence |
title | Fusion and expansion of vitellogenin vesicles during Caenorhabditis elegans intestinal senescence |
title_full | Fusion and expansion of vitellogenin vesicles during Caenorhabditis elegans intestinal senescence |
title_fullStr | Fusion and expansion of vitellogenin vesicles during Caenorhabditis elegans intestinal senescence |
title_full_unstemmed | Fusion and expansion of vitellogenin vesicles during Caenorhabditis elegans intestinal senescence |
title_short | Fusion and expansion of vitellogenin vesicles during Caenorhabditis elegans intestinal senescence |
title_sort | fusion and expansion of vitellogenin vesicles during caenorhabditis elegans intestinal senescence |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9649609/ https://www.ncbi.nlm.nih.gov/pubmed/36199214 http://dx.doi.org/10.1111/acel.13719 |
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