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The Study of Angptl4-Modulated Podocyte Injury in IgA Nephropathy
BACKGROUND: Increasing evidence shows that Angptl4 affects proteinuria in podocytes injured kidney disease, however, whether there is a relationship between Angptl4 and IgA nephropathy (IgAN) has not been studied yet. METHODS: Plasma and urine samples were obtained from 71 patients with IgAN and 61...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7905042/ https://www.ncbi.nlm.nih.gov/pubmed/33643055 http://dx.doi.org/10.3389/fphys.2020.575722 |
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author | Jia, Sha Peng, Xiaofeng Liang, Ludan Zhang, Ying Li, Meng Zhou, Qin Shen, Xiujin Wang, Yucheng Wang, Cuili Feng, Shi Chen, Jianghua Ren, Pingping Jiang, Hong |
author_facet | Jia, Sha Peng, Xiaofeng Liang, Ludan Zhang, Ying Li, Meng Zhou, Qin Shen, Xiujin Wang, Yucheng Wang, Cuili Feng, Shi Chen, Jianghua Ren, Pingping Jiang, Hong |
author_sort | Jia, Sha |
collection | PubMed |
description | BACKGROUND: Increasing evidence shows that Angptl4 affects proteinuria in podocytes injured kidney disease, however, whether there is a relationship between Angptl4 and IgA nephropathy (IgAN) has not been studied yet. METHODS: Plasma and urine samples were obtained from 71 patients with IgAN and 61 healthy controls. Glomeruli from six renal biopsy specimens (three IgAN patients and three healthy controls) were separated by RNA-Seq. Differentially expressed genes (DEGs) related to podocytes and Angptl4 between IgAN patients and healthy controls were performed using the Limma package. Gene set enrichment analysis was used to determine whether there was a statistically significant difference between the two groups. STRING was used to create a protein-protein interaction network of DEGs. Association analysis between Angptl4 levels and clinical features of IgAN was performed. RESULTS: Thirty-three podocyte-related and twenty-three Angpt4-related DEGs were found between IgAN patients and healthy controls. By overlapping the genes, FOS and G6PC were found to be upregulated in IgAN patients, while MMP9 was downregulated in IgAN patients. Plasma and urine Angptl4 levels were closely related to the degree of podocyte injury and urine protein, but not to the protein-creatine ratio. CONCLUSION: Our findings show that Angptl4 levels in plasma and urine are related to podocyte damage and, therefore, may be a promising tool for assessing the severity of IgAN patients to identify and reverse the progression to ESRD. |
format | Online Article Text |
id | pubmed-7905042 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79050422021-02-26 The Study of Angptl4-Modulated Podocyte Injury in IgA Nephropathy Jia, Sha Peng, Xiaofeng Liang, Ludan Zhang, Ying Li, Meng Zhou, Qin Shen, Xiujin Wang, Yucheng Wang, Cuili Feng, Shi Chen, Jianghua Ren, Pingping Jiang, Hong Front Physiol Physiology BACKGROUND: Increasing evidence shows that Angptl4 affects proteinuria in podocytes injured kidney disease, however, whether there is a relationship between Angptl4 and IgA nephropathy (IgAN) has not been studied yet. METHODS: Plasma and urine samples were obtained from 71 patients with IgAN and 61 healthy controls. Glomeruli from six renal biopsy specimens (three IgAN patients and three healthy controls) were separated by RNA-Seq. Differentially expressed genes (DEGs) related to podocytes and Angptl4 between IgAN patients and healthy controls were performed using the Limma package. Gene set enrichment analysis was used to determine whether there was a statistically significant difference between the two groups. STRING was used to create a protein-protein interaction network of DEGs. Association analysis between Angptl4 levels and clinical features of IgAN was performed. RESULTS: Thirty-three podocyte-related and twenty-three Angpt4-related DEGs were found between IgAN patients and healthy controls. By overlapping the genes, FOS and G6PC were found to be upregulated in IgAN patients, while MMP9 was downregulated in IgAN patients. Plasma and urine Angptl4 levels were closely related to the degree of podocyte injury and urine protein, but not to the protein-creatine ratio. CONCLUSION: Our findings show that Angptl4 levels in plasma and urine are related to podocyte damage and, therefore, may be a promising tool for assessing the severity of IgAN patients to identify and reverse the progression to ESRD. Frontiers Media S.A. 2021-02-11 /pmc/articles/PMC7905042/ /pubmed/33643055 http://dx.doi.org/10.3389/fphys.2020.575722 Text en Copyright © 2021 Jia, Peng, Liang, Zhang, Li, Zhou, Shen, Wang, Wang, Feng, Chen, Ren and Jiang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology Jia, Sha Peng, Xiaofeng Liang, Ludan Zhang, Ying Li, Meng Zhou, Qin Shen, Xiujin Wang, Yucheng Wang, Cuili Feng, Shi Chen, Jianghua Ren, Pingping Jiang, Hong The Study of Angptl4-Modulated Podocyte Injury in IgA Nephropathy |
title | The Study of Angptl4-Modulated Podocyte Injury in IgA Nephropathy |
title_full | The Study of Angptl4-Modulated Podocyte Injury in IgA Nephropathy |
title_fullStr | The Study of Angptl4-Modulated Podocyte Injury in IgA Nephropathy |
title_full_unstemmed | The Study of Angptl4-Modulated Podocyte Injury in IgA Nephropathy |
title_short | The Study of Angptl4-Modulated Podocyte Injury in IgA Nephropathy |
title_sort | study of angptl4-modulated podocyte injury in iga nephropathy |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7905042/ https://www.ncbi.nlm.nih.gov/pubmed/33643055 http://dx.doi.org/10.3389/fphys.2020.575722 |
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