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Comparative proteomic analysis of children FSGS FFPE tissues
BACKGROUND: In children, focal segmental glomerulosclerosis (FSGS) is the main cause of steroid resistant nephrotic syndrome (SRNS). To identify specific candidates and the mechanism of steroid resistance, we examined the formalin-fixed paraffin embedded (FFPE) renal tissue protein profiles via liqu...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9743561/ https://www.ncbi.nlm.nih.gov/pubmed/36503536 http://dx.doi.org/10.1186/s12887-022-03764-7 |
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author | Ni, Jiajia Tian, Sha Bai, Lin Lv, Qianying Liu, Jialu Liu, Jiaojiao Fang, Ye Zhai, Yihui Shen, Qian Rao, Jia Ding, Chen Xu, Hong |
author_facet | Ni, Jiajia Tian, Sha Bai, Lin Lv, Qianying Liu, Jialu Liu, Jiaojiao Fang, Ye Zhai, Yihui Shen, Qian Rao, Jia Ding, Chen Xu, Hong |
author_sort | Ni, Jiajia |
collection | PubMed |
description | BACKGROUND: In children, focal segmental glomerulosclerosis (FSGS) is the main cause of steroid resistant nephrotic syndrome (SRNS). To identify specific candidates and the mechanism of steroid resistance, we examined the formalin-fixed paraffin embedded (FFPE) renal tissue protein profiles via liquid chromatography tandem mass spectrometry (LC-MS/MS). METHODS: Renal biopsies from seven steroid-sensitive (SS) and eleven steroid-resistant (SR) children FSGS patients were obtained. We examined the formalin-fixed paraffin embedded (FFPE) renal tissue protein profiles via liquid chromatography tandem mass spectrometry (LC-MS/MS). Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment and Gene Ontology (GO) analysis, as well as the construction of protein-protein interaction (PPI) network were performed. Two proteins were further valiadated by immunohistochemistry staining in FSGS patients and mice models. RESULTS: In total, we quantified more than 4000 proteins, of which 325 were found to be differentially expressed proteins (DEPs) between the SS and SR group (foldchange ≥2, P<0.05). The results of GO revealed that the most significant up-regulated proteins were primarily related to protein transportation, regulation of the complement activation process and cytolysis. Moreover, clustering analysis showed differences in the pathways (lysosome, terminal pathway of complement) between the two groups. Among these potential candidates, validation analyses for LAMP1 and ACSL4 were conducted. LAMP1 was observed to have a higher expression in glomerulus, while ACSL4 was expressed more in tubular epithelial cells. CONCLUSIONS: In this study, the potential mechanism and candidates related to steroid resistance in children FSGS patients were identified. It could be helpful in identifying potential therapeutic targets and predicting outcomes with these proteomic changes for children FSGS patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12887-022-03764-7. |
format | Online Article Text |
id | pubmed-9743561 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-97435612022-12-13 Comparative proteomic analysis of children FSGS FFPE tissues Ni, Jiajia Tian, Sha Bai, Lin Lv, Qianying Liu, Jialu Liu, Jiaojiao Fang, Ye Zhai, Yihui Shen, Qian Rao, Jia Ding, Chen Xu, Hong BMC Pediatr Research BACKGROUND: In children, focal segmental glomerulosclerosis (FSGS) is the main cause of steroid resistant nephrotic syndrome (SRNS). To identify specific candidates and the mechanism of steroid resistance, we examined the formalin-fixed paraffin embedded (FFPE) renal tissue protein profiles via liquid chromatography tandem mass spectrometry (LC-MS/MS). METHODS: Renal biopsies from seven steroid-sensitive (SS) and eleven steroid-resistant (SR) children FSGS patients were obtained. We examined the formalin-fixed paraffin embedded (FFPE) renal tissue protein profiles via liquid chromatography tandem mass spectrometry (LC-MS/MS). Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment and Gene Ontology (GO) analysis, as well as the construction of protein-protein interaction (PPI) network were performed. Two proteins were further valiadated by immunohistochemistry staining in FSGS patients and mice models. RESULTS: In total, we quantified more than 4000 proteins, of which 325 were found to be differentially expressed proteins (DEPs) between the SS and SR group (foldchange ≥2, P<0.05). The results of GO revealed that the most significant up-regulated proteins were primarily related to protein transportation, regulation of the complement activation process and cytolysis. Moreover, clustering analysis showed differences in the pathways (lysosome, terminal pathway of complement) between the two groups. Among these potential candidates, validation analyses for LAMP1 and ACSL4 were conducted. LAMP1 was observed to have a higher expression in glomerulus, while ACSL4 was expressed more in tubular epithelial cells. CONCLUSIONS: In this study, the potential mechanism and candidates related to steroid resistance in children FSGS patients were identified. It could be helpful in identifying potential therapeutic targets and predicting outcomes with these proteomic changes for children FSGS patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12887-022-03764-7. BioMed Central 2022-12-12 /pmc/articles/PMC9743561/ /pubmed/36503536 http://dx.doi.org/10.1186/s12887-022-03764-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Ni, Jiajia Tian, Sha Bai, Lin Lv, Qianying Liu, Jialu Liu, Jiaojiao Fang, Ye Zhai, Yihui Shen, Qian Rao, Jia Ding, Chen Xu, Hong Comparative proteomic analysis of children FSGS FFPE tissues |
title | Comparative proteomic analysis of children FSGS FFPE tissues |
title_full | Comparative proteomic analysis of children FSGS FFPE tissues |
title_fullStr | Comparative proteomic analysis of children FSGS FFPE tissues |
title_full_unstemmed | Comparative proteomic analysis of children FSGS FFPE tissues |
title_short | Comparative proteomic analysis of children FSGS FFPE tissues |
title_sort | comparative proteomic analysis of children fsgs ffpe tissues |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9743561/ https://www.ncbi.nlm.nih.gov/pubmed/36503536 http://dx.doi.org/10.1186/s12887-022-03764-7 |
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