Preferential Propagation of Competent SIX2+ Nephronic Progenitors by LIF/ROCKi Treatment of the Metanephric Mesenchyme

Understanding the mechanisms responsible for nephrogenic stem cell preservation and commitment is fundamental to harnessing the potential of the metanephric mesenchyme (MM) for nephron regeneration. Accordingly, we established a culture model that preferentially expands the MM SIX2+ progenitor pool...

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Main Authors: Shunsuke Tanigawa, Nirmala Sharma, Michael D. Hall, Ryuichi Nishinakamura, Alan O. Perantoni
Format: Article
Language:English
Published: Elsevier 2015-09-01
Series:Stem Cell Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2213671115002210
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spelling doaj-977d3a35a00f4401a0e4a606ad0cc8722020-11-24T23:53:20ZengElsevierStem Cell Reports2213-67112015-09-015343544710.1016/j.stemcr.2015.07.015Preferential Propagation of Competent SIX2+ Nephronic Progenitors by LIF/ROCKi Treatment of the Metanephric MesenchymeShunsuke Tanigawa0Nirmala Sharma1Michael D. Hall2Ryuichi Nishinakamura3Alan O. Perantoni4National Cancer Institute-Frederick, Frederick, MD 21702, USANational Cancer Institute-Frederick, Frederick, MD 21702, USANational Cancer Institute-Frederick, Frederick, MD 21702, USADepartment of Kidney Development, Institute of Molecular Embryology and Genetics, Kumamoto University, 2-2-1 Honjo, Kumamoto 860-0811, JapanNational Cancer Institute-Frederick, Frederick, MD 21702, USAUnderstanding the mechanisms responsible for nephrogenic stem cell preservation and commitment is fundamental to harnessing the potential of the metanephric mesenchyme (MM) for nephron regeneration. Accordingly, we established a culture model that preferentially expands the MM SIX2+ progenitor pool using leukemia inhibitory factor (LIF), a Rho kinase inhibitor (ROCKi), and extracellular matrix. Passaged MM cells express the key stem cell regulators Six2 and Pax2 and remain competent to respond to WNT4 induction and form mature tubular epithelia and glomeruli. Mechanistically, LIF activates STAT, which binds to a Stat consensus sequence in the Six2 proximal promoter and sustains SIX2 levels. ROCKi, on the other hand, attenuates the LIF-induced differentiation activity of JNK. Concomitantly, the combination of LIF/ROCKi upregulates Slug expression and activates YAP, which maintains SIX2, PAX2, and SALL1. Using this novel model, our study underscores the pivotal roles of SIX2 and YAP in MM stem cell stability.http://www.sciencedirect.com/science/article/pii/S2213671115002210
collection DOAJ
language English
format Article
sources DOAJ
author Shunsuke Tanigawa
Nirmala Sharma
Michael D. Hall
Ryuichi Nishinakamura
Alan O. Perantoni
spellingShingle Shunsuke Tanigawa
Nirmala Sharma
Michael D. Hall
Ryuichi Nishinakamura
Alan O. Perantoni
Preferential Propagation of Competent SIX2+ Nephronic Progenitors by LIF/ROCKi Treatment of the Metanephric Mesenchyme
Stem Cell Reports
author_facet Shunsuke Tanigawa
Nirmala Sharma
Michael D. Hall
Ryuichi Nishinakamura
Alan O. Perantoni
author_sort Shunsuke Tanigawa
title Preferential Propagation of Competent SIX2+ Nephronic Progenitors by LIF/ROCKi Treatment of the Metanephric Mesenchyme
title_short Preferential Propagation of Competent SIX2+ Nephronic Progenitors by LIF/ROCKi Treatment of the Metanephric Mesenchyme
title_full Preferential Propagation of Competent SIX2+ Nephronic Progenitors by LIF/ROCKi Treatment of the Metanephric Mesenchyme
title_fullStr Preferential Propagation of Competent SIX2+ Nephronic Progenitors by LIF/ROCKi Treatment of the Metanephric Mesenchyme
title_full_unstemmed Preferential Propagation of Competent SIX2+ Nephronic Progenitors by LIF/ROCKi Treatment of the Metanephric Mesenchyme
title_sort preferential propagation of competent six2+ nephronic progenitors by lif/rocki treatment of the metanephric mesenchyme
publisher Elsevier
series Stem Cell Reports
issn 2213-6711
publishDate 2015-09-01
description Understanding the mechanisms responsible for nephrogenic stem cell preservation and commitment is fundamental to harnessing the potential of the metanephric mesenchyme (MM) for nephron regeneration. Accordingly, we established a culture model that preferentially expands the MM SIX2+ progenitor pool using leukemia inhibitory factor (LIF), a Rho kinase inhibitor (ROCKi), and extracellular matrix. Passaged MM cells express the key stem cell regulators Six2 and Pax2 and remain competent to respond to WNT4 induction and form mature tubular epithelia and glomeruli. Mechanistically, LIF activates STAT, which binds to a Stat consensus sequence in the Six2 proximal promoter and sustains SIX2 levels. ROCKi, on the other hand, attenuates the LIF-induced differentiation activity of JNK. Concomitantly, the combination of LIF/ROCKi upregulates Slug expression and activates YAP, which maintains SIX2, PAX2, and SALL1. Using this novel model, our study underscores the pivotal roles of SIX2 and YAP in MM stem cell stability.
url http://www.sciencedirect.com/science/article/pii/S2213671115002210
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