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Caloric restriction alleviates aging-related fibrosis of kidney through downregulation of miR-21 in extracellular vesicles
Glomerulosclerosis and renal interstitial fibrosis occur with the aging kidney. In this study, we examined the expression of miR-21, peroxisome proliferator-activated receptor(PPARα), hypoxia-inducible factor(HIF-1α) in the kidney of 3-month-old rats fed ad libitum (YAL), 24-month-old rats fed ad li...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7585074/ https://www.ncbi.nlm.nih.gov/pubmed/32963130 http://dx.doi.org/10.18632/aging.103591 |
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author | Liu, Jin-rui Cai, Guang-yan Ning, Yi-chun Wang, Jing-chao Lv, Yang Guo, Ya-nan Fu, Bo Hong, Quan Sun, Xue-feng Chen, Xiang-mei |
author_facet | Liu, Jin-rui Cai, Guang-yan Ning, Yi-chun Wang, Jing-chao Lv, Yang Guo, Ya-nan Fu, Bo Hong, Quan Sun, Xue-feng Chen, Xiang-mei |
author_sort | Liu, Jin-rui |
collection | PubMed |
description | Glomerulosclerosis and renal interstitial fibrosis occur with the aging kidney. In this study, we examined the expression of miR-21, peroxisome proliferator-activated receptor(PPARα), hypoxia-inducible factor(HIF-1α) in the kidney of 3-month-old rats fed ad libitum (YAL), 24-month-old rats fed ad libitum (OAL) and 24-month-old rats subjected to a 70% calorie-restricted diet for 8 months (OCR). We found long-term caloric restriction (CR) ameliorated aging and aging-related fibrosis. CR ameliorated the increment of miR-21 and HIF-1α, as well as the decrement of PPARα in old ad libitum group. Human proximal tubular cells (HPTCs) presented phenotypes of senescence and epithelial to mesenchymal transition (EMT) under high-glucose conditions, in which senescence occurred earlier than EMT. Senescent cells secreted extracellular vesicles (EVs) which contained miR-21 into the recipient cells. Inhibiting miR-21 of donor cells prevented the occurrence of EMT in recipient cells. In addition, miR-21 induced EMT through targeting PPARα protein and consequently enhancing HIF-1α expression, although other pathways cannot be ruled out. These findings demonstrated that miR-21-containing EVs derived from the senescent cells could facilitate EMT of HPTCs via PPARα-HIF-1α signaling pathway. Long-term caloric restriction and caloric restriction mimetics alleviated aging-related-fibrosis of kidney through downregulation of miR-21. |
format | Online Article Text |
id | pubmed-7585074 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-75850742020-11-03 Caloric restriction alleviates aging-related fibrosis of kidney through downregulation of miR-21 in extracellular vesicles Liu, Jin-rui Cai, Guang-yan Ning, Yi-chun Wang, Jing-chao Lv, Yang Guo, Ya-nan Fu, Bo Hong, Quan Sun, Xue-feng Chen, Xiang-mei Aging (Albany NY) Research Paper Glomerulosclerosis and renal interstitial fibrosis occur with the aging kidney. In this study, we examined the expression of miR-21, peroxisome proliferator-activated receptor(PPARα), hypoxia-inducible factor(HIF-1α) in the kidney of 3-month-old rats fed ad libitum (YAL), 24-month-old rats fed ad libitum (OAL) and 24-month-old rats subjected to a 70% calorie-restricted diet for 8 months (OCR). We found long-term caloric restriction (CR) ameliorated aging and aging-related fibrosis. CR ameliorated the increment of miR-21 and HIF-1α, as well as the decrement of PPARα in old ad libitum group. Human proximal tubular cells (HPTCs) presented phenotypes of senescence and epithelial to mesenchymal transition (EMT) under high-glucose conditions, in which senescence occurred earlier than EMT. Senescent cells secreted extracellular vesicles (EVs) which contained miR-21 into the recipient cells. Inhibiting miR-21 of donor cells prevented the occurrence of EMT in recipient cells. In addition, miR-21 induced EMT through targeting PPARα protein and consequently enhancing HIF-1α expression, although other pathways cannot be ruled out. These findings demonstrated that miR-21-containing EVs derived from the senescent cells could facilitate EMT of HPTCs via PPARα-HIF-1α signaling pathway. Long-term caloric restriction and caloric restriction mimetics alleviated aging-related-fibrosis of kidney through downregulation of miR-21. Impact Journals 2020-08-27 /pmc/articles/PMC7585074/ /pubmed/32963130 http://dx.doi.org/10.18632/aging.103591 Text en Copyright: © 2020 Liu et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Liu, Jin-rui Cai, Guang-yan Ning, Yi-chun Wang, Jing-chao Lv, Yang Guo, Ya-nan Fu, Bo Hong, Quan Sun, Xue-feng Chen, Xiang-mei Caloric restriction alleviates aging-related fibrosis of kidney through downregulation of miR-21 in extracellular vesicles |
title | Caloric restriction alleviates aging-related fibrosis of kidney through downregulation of miR-21 in extracellular vesicles |
title_full | Caloric restriction alleviates aging-related fibrosis of kidney through downregulation of miR-21 in extracellular vesicles |
title_fullStr | Caloric restriction alleviates aging-related fibrosis of kidney through downregulation of miR-21 in extracellular vesicles |
title_full_unstemmed | Caloric restriction alleviates aging-related fibrosis of kidney through downregulation of miR-21 in extracellular vesicles |
title_short | Caloric restriction alleviates aging-related fibrosis of kidney through downregulation of miR-21 in extracellular vesicles |
title_sort | caloric restriction alleviates aging-related fibrosis of kidney through downregulation of mir-21 in extracellular vesicles |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7585074/ https://www.ncbi.nlm.nih.gov/pubmed/32963130 http://dx.doi.org/10.18632/aging.103591 |
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