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Endotrophin neutralization through targeted antibody treatment protects from renal fibrosis in a podocyte ablation model
OBJECTIVE: Renal fibrosis is a hallmark for chronic kidney disease (CKD), and often leads to end stage renal disease (ESRD). However, limited interventions are available clinically to ameliorate or reverse renal fibrosis. METHODS: Herein, we evaluated whether blockade of endotrophin through neutrali...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9918787/ https://www.ncbi.nlm.nih.gov/pubmed/36696925 http://dx.doi.org/10.1016/j.molmet.2023.101680 |
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author | An, Yu A. Xiong, Wei Chen, Shiuhwei Bu, Dawei Rutkowski, Joseph M. Berger, Joel P. Kusminski, Christine M. Zhang, Ningyan An, Zhiqiang Scherer, Philipp E. |
author_facet | An, Yu A. Xiong, Wei Chen, Shiuhwei Bu, Dawei Rutkowski, Joseph M. Berger, Joel P. Kusminski, Christine M. Zhang, Ningyan An, Zhiqiang Scherer, Philipp E. |
author_sort | An, Yu A. |
collection | PubMed |
description | OBJECTIVE: Renal fibrosis is a hallmark for chronic kidney disease (CKD), and often leads to end stage renal disease (ESRD). However, limited interventions are available clinically to ameliorate or reverse renal fibrosis. METHODS: Herein, we evaluated whether blockade of endotrophin through neutralizing antibodies protects from renal fibrosis in the podocyte insult model (the “POD-ATTAC” mouse). We determined the therapeutic effects of endotrophin targeted antibody through assessing renal function, renal inflammation and fibrosis at histological and transcriptional levels, and podocyte regeneration. RESULTS: We demonstrated that neutralizing endotrophin antibody treatment significantly ameliorates renal fibrosis at the transcriptional, morphological, and functional levels. In the antibody treatment group, expression of pro-inflammatory and pro-fibrotic genes was significantly reduced, normal renal structures were restored, collagen deposition was decreased, and proteinuria and renal function were improved. We further performed a lineage tracing study confirming that podocytes regenerate as de novo podocytes upon injury and loss, and blockade of endotrophin efficiently enhances podocyte-specific marker expressions. CONCLUSION: Combined, we provide pre-clinical evidence supporting neutralizing endotrophin as a promising therapy for intervening with renal fibrosis in CKD, and potentially in other chronic fibro-inflammatory diseases. |
format | Online Article Text |
id | pubmed-9918787 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-99187872023-02-12 Endotrophin neutralization through targeted antibody treatment protects from renal fibrosis in a podocyte ablation model An, Yu A. Xiong, Wei Chen, Shiuhwei Bu, Dawei Rutkowski, Joseph M. Berger, Joel P. Kusminski, Christine M. Zhang, Ningyan An, Zhiqiang Scherer, Philipp E. Mol Metab Brief Communication OBJECTIVE: Renal fibrosis is a hallmark for chronic kidney disease (CKD), and often leads to end stage renal disease (ESRD). However, limited interventions are available clinically to ameliorate or reverse renal fibrosis. METHODS: Herein, we evaluated whether blockade of endotrophin through neutralizing antibodies protects from renal fibrosis in the podocyte insult model (the “POD-ATTAC” mouse). We determined the therapeutic effects of endotrophin targeted antibody through assessing renal function, renal inflammation and fibrosis at histological and transcriptional levels, and podocyte regeneration. RESULTS: We demonstrated that neutralizing endotrophin antibody treatment significantly ameliorates renal fibrosis at the transcriptional, morphological, and functional levels. In the antibody treatment group, expression of pro-inflammatory and pro-fibrotic genes was significantly reduced, normal renal structures were restored, collagen deposition was decreased, and proteinuria and renal function were improved. We further performed a lineage tracing study confirming that podocytes regenerate as de novo podocytes upon injury and loss, and blockade of endotrophin efficiently enhances podocyte-specific marker expressions. CONCLUSION: Combined, we provide pre-clinical evidence supporting neutralizing endotrophin as a promising therapy for intervening with renal fibrosis in CKD, and potentially in other chronic fibro-inflammatory diseases. Elsevier 2023-01-22 /pmc/articles/PMC9918787/ /pubmed/36696925 http://dx.doi.org/10.1016/j.molmet.2023.101680 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Brief Communication An, Yu A. Xiong, Wei Chen, Shiuhwei Bu, Dawei Rutkowski, Joseph M. Berger, Joel P. Kusminski, Christine M. Zhang, Ningyan An, Zhiqiang Scherer, Philipp E. Endotrophin neutralization through targeted antibody treatment protects from renal fibrosis in a podocyte ablation model |
title | Endotrophin neutralization through targeted antibody treatment protects from renal fibrosis in a podocyte ablation model |
title_full | Endotrophin neutralization through targeted antibody treatment protects from renal fibrosis in a podocyte ablation model |
title_fullStr | Endotrophin neutralization through targeted antibody treatment protects from renal fibrosis in a podocyte ablation model |
title_full_unstemmed | Endotrophin neutralization through targeted antibody treatment protects from renal fibrosis in a podocyte ablation model |
title_short | Endotrophin neutralization through targeted antibody treatment protects from renal fibrosis in a podocyte ablation model |
title_sort | endotrophin neutralization through targeted antibody treatment protects from renal fibrosis in a podocyte ablation model |
topic | Brief Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9918787/ https://www.ncbi.nlm.nih.gov/pubmed/36696925 http://dx.doi.org/10.1016/j.molmet.2023.101680 |
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