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Renal defects associated with improper polarization of the CRB and DLG polarity complexes in MALS-3 knockout mice
Kidney development and physiology require polarization of epithelia that line renal tubules. Genetic studies show that polarization of invertebrate epithelia requires the crumbs, partition-defective-3, and discs large complexes. These evolutionarily conserved protein complexes occur in mammalian kid...
Autores principales: | , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2064744/ https://www.ncbi.nlm.nih.gov/pubmed/17923534 http://dx.doi.org/10.1083/jcb.200702054 |
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author | Olsen, Olav Funke, Lars Long, Jia-fu Fukata, Masaki Kazuta, Toshinari Trinidad, Jonathan C. Moore, Kimberly A. Misawa, Hidemi Welling, Paul A. Burlingame, Alma L. Zhang, Mingjie Bredt, David S. |
author_facet | Olsen, Olav Funke, Lars Long, Jia-fu Fukata, Masaki Kazuta, Toshinari Trinidad, Jonathan C. Moore, Kimberly A. Misawa, Hidemi Welling, Paul A. Burlingame, Alma L. Zhang, Mingjie Bredt, David S. |
author_sort | Olsen, Olav |
collection | PubMed |
description | Kidney development and physiology require polarization of epithelia that line renal tubules. Genetic studies show that polarization of invertebrate epithelia requires the crumbs, partition-defective-3, and discs large complexes. These evolutionarily conserved protein complexes occur in mammalian kidney; however, their role in renal development remains poorly defined. Here, we find that mice lacking the small PDZ protein mammalian LIN-7c (MALS-3) have hypomorphic, cystic, and fibrotic kidneys. Proteomic analysis defines MALS-3 as the only known core component of both the crumbs and discs large cell polarity complexes. MALS-3 mediates stable assembly of the crumbs tight junction complex and the discs large basolateral complex, and these complexes are disrupted in renal epithelia from MALS-3 knockout mice. Interestingly, MALS-3 controls apico-basal polarity preferentially in epithelia derived from metanephric mesenchyme, and defects in kidney architecture owe solely to MALS expression in these epithelia. These studies demonstrate that defects in epithelial cell polarization can cause cystic and fibrotic renal disease. |
format | Text |
id | pubmed-2064744 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-20647442008-04-08 Renal defects associated with improper polarization of the CRB and DLG polarity complexes in MALS-3 knockout mice Olsen, Olav Funke, Lars Long, Jia-fu Fukata, Masaki Kazuta, Toshinari Trinidad, Jonathan C. Moore, Kimberly A. Misawa, Hidemi Welling, Paul A. Burlingame, Alma L. Zhang, Mingjie Bredt, David S. J Cell Biol Research Articles Kidney development and physiology require polarization of epithelia that line renal tubules. Genetic studies show that polarization of invertebrate epithelia requires the crumbs, partition-defective-3, and discs large complexes. These evolutionarily conserved protein complexes occur in mammalian kidney; however, their role in renal development remains poorly defined. Here, we find that mice lacking the small PDZ protein mammalian LIN-7c (MALS-3) have hypomorphic, cystic, and fibrotic kidneys. Proteomic analysis defines MALS-3 as the only known core component of both the crumbs and discs large cell polarity complexes. MALS-3 mediates stable assembly of the crumbs tight junction complex and the discs large basolateral complex, and these complexes are disrupted in renal epithelia from MALS-3 knockout mice. Interestingly, MALS-3 controls apico-basal polarity preferentially in epithelia derived from metanephric mesenchyme, and defects in kidney architecture owe solely to MALS expression in these epithelia. These studies demonstrate that defects in epithelial cell polarization can cause cystic and fibrotic renal disease. The Rockefeller University Press 2007-10-08 /pmc/articles/PMC2064744/ /pubmed/17923534 http://dx.doi.org/10.1083/jcb.200702054 Text en Copyright © 2007, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Research Articles Olsen, Olav Funke, Lars Long, Jia-fu Fukata, Masaki Kazuta, Toshinari Trinidad, Jonathan C. Moore, Kimberly A. Misawa, Hidemi Welling, Paul A. Burlingame, Alma L. Zhang, Mingjie Bredt, David S. Renal defects associated with improper polarization of the CRB and DLG polarity complexes in MALS-3 knockout mice |
title | Renal defects associated with improper polarization of the CRB and DLG polarity complexes in MALS-3 knockout mice |
title_full | Renal defects associated with improper polarization of the CRB and DLG polarity complexes in MALS-3 knockout mice |
title_fullStr | Renal defects associated with improper polarization of the CRB and DLG polarity complexes in MALS-3 knockout mice |
title_full_unstemmed | Renal defects associated with improper polarization of the CRB and DLG polarity complexes in MALS-3 knockout mice |
title_short | Renal defects associated with improper polarization of the CRB and DLG polarity complexes in MALS-3 knockout mice |
title_sort | renal defects associated with improper polarization of the crb and dlg polarity complexes in mals-3 knockout mice |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2064744/ https://www.ncbi.nlm.nih.gov/pubmed/17923534 http://dx.doi.org/10.1083/jcb.200702054 |
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