Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
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
_version_ 1784886663508393984
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
work_keys_str_mv AT anyua endotrophinneutralizationthroughtargetedantibodytreatmentprotectsfromrenalfibrosisinapodocyteablationmodel
AT xiongwei endotrophinneutralizationthroughtargetedantibodytreatmentprotectsfromrenalfibrosisinapodocyteablationmodel
AT chenshiuhwei endotrophinneutralizationthroughtargetedantibodytreatmentprotectsfromrenalfibrosisinapodocyteablationmodel
AT budawei endotrophinneutralizationthroughtargetedantibodytreatmentprotectsfromrenalfibrosisinapodocyteablationmodel
AT rutkowskijosephm endotrophinneutralizationthroughtargetedantibodytreatmentprotectsfromrenalfibrosisinapodocyteablationmodel
AT bergerjoelp endotrophinneutralizationthroughtargetedantibodytreatmentprotectsfromrenalfibrosisinapodocyteablationmodel
AT kusminskichristinem endotrophinneutralizationthroughtargetedantibodytreatmentprotectsfromrenalfibrosisinapodocyteablationmodel
AT zhangningyan endotrophinneutralizationthroughtargetedantibodytreatmentprotectsfromrenalfibrosisinapodocyteablationmodel
AT anzhiqiang endotrophinneutralizationthroughtargetedantibodytreatmentprotectsfromrenalfibrosisinapodocyteablationmodel
AT schererphilippe endotrophinneutralizationthroughtargetedantibodytreatmentprotectsfromrenalfibrosisinapodocyteablationmodel