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Role of calcineurin (CN) in kidney glomerular podocyte: CN inhibitor ameliorated proteinuria by inhibiting the redistribution of CN at the slit diaphragm

Although calcineurin (CN) is distributed in many cell types and functions in regulating cell functions, the precise roles of CN remained in each type of the cells are not well understood yet. A CN inhibitor (CNI) has been used for steroid‐resistant nephrotic syndrome. A CNI is assumed to ameliorate...

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Autores principales: Wakamatsu, Ayako, Fukusumi, Yoshiyasu, Hasegawa, Eriko, Tomita, Masayuki, Watanabe, Toru, Narita, Ichiei, Kawachi, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4814882/
https://www.ncbi.nlm.nih.gov/pubmed/27009276
http://dx.doi.org/10.14814/phy2.12679
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author Wakamatsu, Ayako
Fukusumi, Yoshiyasu
Hasegawa, Eriko
Tomita, Masayuki
Watanabe, Toru
Narita, Ichiei
Kawachi, Hiroshi
author_facet Wakamatsu, Ayako
Fukusumi, Yoshiyasu
Hasegawa, Eriko
Tomita, Masayuki
Watanabe, Toru
Narita, Ichiei
Kawachi, Hiroshi
author_sort Wakamatsu, Ayako
collection PubMed
description Although calcineurin (CN) is distributed in many cell types and functions in regulating cell functions, the precise roles of CN remained in each type of the cells are not well understood yet. A CN inhibitor (CNI) has been used for steroid‐resistant nephrotic syndrome. A CNI is assumed to ameliorate proteinuria by preventing the overproduction of T‐cell cytokines. However, recent reports suggest that CNI has a direct effect on podocyte. It is accepted that a slit diaphragm (SD), a unique cell–cell junction of podocytes, is a critical barrier preventing a leak of plasma protein into urine. Therefore, we hypothesized that CNI has an effect on the SD. In this study, we analyzed the expression of CN in physiological and in the nephrotic model caused by the antibody against nephrin, a critical component of the SD. We observed that CN is expressed at the SD in normal rat and human kidney sections and has an interaction with nephrin. The staining of CN at the SD was reduced in the nephrotic model, while CN activity in glomeruli was increased. We also observed that the treatment with tacrolimus, a CNI, in this nephrotic model suppressed the redistribution of CN, nephrin, and other SD components and ameliorated proteinuria. These observations suggested that the redistribution and the activation of CN may participate in the development of the SD injury.
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spelling pubmed-48148822016-04-11 Role of calcineurin (CN) in kidney glomerular podocyte: CN inhibitor ameliorated proteinuria by inhibiting the redistribution of CN at the slit diaphragm Wakamatsu, Ayako Fukusumi, Yoshiyasu Hasegawa, Eriko Tomita, Masayuki Watanabe, Toru Narita, Ichiei Kawachi, Hiroshi Physiol Rep Original Research Although calcineurin (CN) is distributed in many cell types and functions in regulating cell functions, the precise roles of CN remained in each type of the cells are not well understood yet. A CN inhibitor (CNI) has been used for steroid‐resistant nephrotic syndrome. A CNI is assumed to ameliorate proteinuria by preventing the overproduction of T‐cell cytokines. However, recent reports suggest that CNI has a direct effect on podocyte. It is accepted that a slit diaphragm (SD), a unique cell–cell junction of podocytes, is a critical barrier preventing a leak of plasma protein into urine. Therefore, we hypothesized that CNI has an effect on the SD. In this study, we analyzed the expression of CN in physiological and in the nephrotic model caused by the antibody against nephrin, a critical component of the SD. We observed that CN is expressed at the SD in normal rat and human kidney sections and has an interaction with nephrin. The staining of CN at the SD was reduced in the nephrotic model, while CN activity in glomeruli was increased. We also observed that the treatment with tacrolimus, a CNI, in this nephrotic model suppressed the redistribution of CN, nephrin, and other SD components and ameliorated proteinuria. These observations suggested that the redistribution and the activation of CN may participate in the development of the SD injury. John Wiley and Sons Inc. 2016-03-23 /pmc/articles/PMC4814882/ /pubmed/27009276 http://dx.doi.org/10.14814/phy2.12679 Text en © 2016 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Wakamatsu, Ayako
Fukusumi, Yoshiyasu
Hasegawa, Eriko
Tomita, Masayuki
Watanabe, Toru
Narita, Ichiei
Kawachi, Hiroshi
Role of calcineurin (CN) in kidney glomerular podocyte: CN inhibitor ameliorated proteinuria by inhibiting the redistribution of CN at the slit diaphragm
title Role of calcineurin (CN) in kidney glomerular podocyte: CN inhibitor ameliorated proteinuria by inhibiting the redistribution of CN at the slit diaphragm
title_full Role of calcineurin (CN) in kidney glomerular podocyte: CN inhibitor ameliorated proteinuria by inhibiting the redistribution of CN at the slit diaphragm
title_fullStr Role of calcineurin (CN) in kidney glomerular podocyte: CN inhibitor ameliorated proteinuria by inhibiting the redistribution of CN at the slit diaphragm
title_full_unstemmed Role of calcineurin (CN) in kidney glomerular podocyte: CN inhibitor ameliorated proteinuria by inhibiting the redistribution of CN at the slit diaphragm
title_short Role of calcineurin (CN) in kidney glomerular podocyte: CN inhibitor ameliorated proteinuria by inhibiting the redistribution of CN at the slit diaphragm
title_sort role of calcineurin (cn) in kidney glomerular podocyte: cn inhibitor ameliorated proteinuria by inhibiting the redistribution of cn at the slit diaphragm
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4814882/
https://www.ncbi.nlm.nih.gov/pubmed/27009276
http://dx.doi.org/10.14814/phy2.12679
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