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Protein phosphatase 2A modulates podocyte maturation and glomerular functional integrity in mice

BACKGROUND: Protein phosphorylation & dephosphorylation are ubiquitous cellular processes that allow for the nuanced and reversible regulation of protein activity. Protein phosphatase 2A (PP2A) is a multifunction phosphatase that is well expressed in all cell types of kidney during early renal d...

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Autores principales: Zhu, Xiujuan, Ye, Yuhong, Xu, Chengxian, Gao, Cunji, Zhang, Yingying, Zhou, Jing, Lin, Weiqiang, Mao, Jianhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6685276/
https://www.ncbi.nlm.nih.gov/pubmed/31387591
http://dx.doi.org/10.1186/s12964-019-0402-y
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author Zhu, Xiujuan
Ye, Yuhong
Xu, Chengxian
Gao, Cunji
Zhang, Yingying
Zhou, Jing
Lin, Weiqiang
Mao, Jianhua
author_facet Zhu, Xiujuan
Ye, Yuhong
Xu, Chengxian
Gao, Cunji
Zhang, Yingying
Zhou, Jing
Lin, Weiqiang
Mao, Jianhua
author_sort Zhu, Xiujuan
collection PubMed
description BACKGROUND: Protein phosphorylation & dephosphorylation are ubiquitous cellular processes that allow for the nuanced and reversible regulation of protein activity. Protein phosphatase 2A (PP2A) is a multifunction phosphatase that is well expressed in all cell types of kidney during early renal development, though its functions in kidney remains to be elucidated. METHODS: PP2A conditional knock-out mice was generated with PP2A fl/fl mice that were crossed with Podocin-Cre mice. The phenotype of Pod-PP2A–KO mice (homozygous for the floxed PP2A allele with Podocin-Cre) and littermate PP2A fl/fl controls (homozygous for the PP2A allele but lacking Podocin-Cre) were further studied. Primary podocytes isolated from the Pod-PP2A-KO mice were cultured and they were then employed with sing label-free nano-LC − MS/MS technology on a Q-exactive followed by SIEVE processing to identify possible target molecular entities for the dephosphorylation effect of PP2A, in which Western blot and immunofluorescent staining were used to analyze further. RESULTS: Pod-PP2A–KO mice were developed with weight loss, growth retardation, proteinuria, glomerulopathy and foot process effacement, together with reduced expression of some slit diaphragm molecules and cytoskeleton rearrangement of podocytes. Y box protein 1 (YB-1) was identified to be the target molecule for dephosphorylation effect of PP2A. Furthermore, YB-1 phosphorylation was up-regulated in the Pod-PP2A–KO mice in contrast to the wild type controls, while total and un-phosphorylated YB-1 both was moderately down-regulated in podocytes from the Pod-PP2A-KO mice. CONCLUSION: Our study revealed the important role of PP2A in regulating the development of foot processes and fully differentiated podocytes whereas fine-tuning of YB-1 via a post-translational modification by PP2A regulating its activity might be crucial for the functional integrity of podocytes and glomerular filtration barrier. GRAPHIC ABSTRACT: [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12964-019-0402-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-66852762019-08-12 Protein phosphatase 2A modulates podocyte maturation and glomerular functional integrity in mice Zhu, Xiujuan Ye, Yuhong Xu, Chengxian Gao, Cunji Zhang, Yingying Zhou, Jing Lin, Weiqiang Mao, Jianhua Cell Commun Signal Research BACKGROUND: Protein phosphorylation & dephosphorylation are ubiquitous cellular processes that allow for the nuanced and reversible regulation of protein activity. Protein phosphatase 2A (PP2A) is a multifunction phosphatase that is well expressed in all cell types of kidney during early renal development, though its functions in kidney remains to be elucidated. METHODS: PP2A conditional knock-out mice was generated with PP2A fl/fl mice that were crossed with Podocin-Cre mice. The phenotype of Pod-PP2A–KO mice (homozygous for the floxed PP2A allele with Podocin-Cre) and littermate PP2A fl/fl controls (homozygous for the PP2A allele but lacking Podocin-Cre) were further studied. Primary podocytes isolated from the Pod-PP2A-KO mice were cultured and they were then employed with sing label-free nano-LC − MS/MS technology on a Q-exactive followed by SIEVE processing to identify possible target molecular entities for the dephosphorylation effect of PP2A, in which Western blot and immunofluorescent staining were used to analyze further. RESULTS: Pod-PP2A–KO mice were developed with weight loss, growth retardation, proteinuria, glomerulopathy and foot process effacement, together with reduced expression of some slit diaphragm molecules and cytoskeleton rearrangement of podocytes. Y box protein 1 (YB-1) was identified to be the target molecule for dephosphorylation effect of PP2A. Furthermore, YB-1 phosphorylation was up-regulated in the Pod-PP2A–KO mice in contrast to the wild type controls, while total and un-phosphorylated YB-1 both was moderately down-regulated in podocytes from the Pod-PP2A-KO mice. CONCLUSION: Our study revealed the important role of PP2A in regulating the development of foot processes and fully differentiated podocytes whereas fine-tuning of YB-1 via a post-translational modification by PP2A regulating its activity might be crucial for the functional integrity of podocytes and glomerular filtration barrier. GRAPHIC ABSTRACT: [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12964-019-0402-y) contains supplementary material, which is available to authorized users. BioMed Central 2019-08-06 /pmc/articles/PMC6685276/ /pubmed/31387591 http://dx.doi.org/10.1186/s12964-019-0402-y Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Zhu, Xiujuan
Ye, Yuhong
Xu, Chengxian
Gao, Cunji
Zhang, Yingying
Zhou, Jing
Lin, Weiqiang
Mao, Jianhua
Protein phosphatase 2A modulates podocyte maturation and glomerular functional integrity in mice
title Protein phosphatase 2A modulates podocyte maturation and glomerular functional integrity in mice
title_full Protein phosphatase 2A modulates podocyte maturation and glomerular functional integrity in mice
title_fullStr Protein phosphatase 2A modulates podocyte maturation and glomerular functional integrity in mice
title_full_unstemmed Protein phosphatase 2A modulates podocyte maturation and glomerular functional integrity in mice
title_short Protein phosphatase 2A modulates podocyte maturation and glomerular functional integrity in mice
title_sort protein phosphatase 2a modulates podocyte maturation and glomerular functional integrity in mice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6685276/
https://www.ncbi.nlm.nih.gov/pubmed/31387591
http://dx.doi.org/10.1186/s12964-019-0402-y
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