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The role of long-term label-retaining cells in the regeneration of adult mouse kidney after ischemia/reperfusion injury
BACKGROUND: Label-retaining cells (LRCs) have been recognized as rare stem and progenitor-like cells, but their complex biological features in renal repair at the cellular level have never been reported. This study was conducted to evaluate whether LRCs in kidney are indeed renal stem/progenitor cel...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4852428/ https://www.ncbi.nlm.nih.gov/pubmed/27137761 http://dx.doi.org/10.1186/s13287-016-0324-1 |
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author | Liu, Xiangchun Liu, Haiying Sun, Lina Chen, Zhixin Nie, Huibin Sun, Aili Liu, Gang Guan, Guangju |
author_facet | Liu, Xiangchun Liu, Haiying Sun, Lina Chen, Zhixin Nie, Huibin Sun, Aili Liu, Gang Guan, Guangju |
author_sort | Liu, Xiangchun |
collection | PubMed |
description | BACKGROUND: Label-retaining cells (LRCs) have been recognized as rare stem and progenitor-like cells, but their complex biological features in renal repair at the cellular level have never been reported. This study was conducted to evaluate whether LRCs in kidney are indeed renal stem/progenitor cells and to delineate their potential role in kidney regeneration. METHODS: We utilized a long-term pulse chase of 5-bromo-2'-deoxyuridine (BrdU)-labeled cells in C57BL/6J mice to identify renal LRCs. We tracked the precise morphological characteristics and locations of BrdU(+)LRCs by both immunohistochemistry and immunofluorescence. To examine whether these BrdU(+)LRCs contribute to the repair of acute kidney injury, we analyzed biological characteristics of BrdU(+)LRCs in mice after ischemia/reperfusion (I/R) injury. RESULTS: The findings revealed that the nuclei of BrdU(+) LRCs exhibited different morphological characteristics in normal adult kidneys, including nuclei in pairs or scattered, fragmented or intact, strongly or weakly positive. Only 24.3 ± 1.5 % of BrdU(+) LRCs co-expressed with Ki67 and 9.1 ± 1.4 % of BrdU(+) LRCs were positive for TUNEL following renal I/R injury. Interestingly, we found that newly regenerated cells formed a niche-like structure and LRCs in pairs tended to locate in this structure, but the number of those LRCs was very low. We found a few scattered LRCs co-expressed Lotus tetragonolobus agglutinin (LTA) in the early phase of injury, suggesting differentiation of those LRCs in mouse kidney. CONCLUSIONS: Our findings suggest that LRCs are not a simple type of slow-cycling cells in adult kidneys, indicating a limited role of these cells in the regeneration of I/R injured kidney. Thus, LRCs cannot reliably be considered stem/progenitor cells in the regeneration of adult mouse kidney. When researchers use this technique to study the cellular basis of renal repair, these complex features of renal LRCs and the purity of real stem cells among renal LRCs should be considered. |
format | Online Article Text |
id | pubmed-4852428 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48524282016-05-03 The role of long-term label-retaining cells in the regeneration of adult mouse kidney after ischemia/reperfusion injury Liu, Xiangchun Liu, Haiying Sun, Lina Chen, Zhixin Nie, Huibin Sun, Aili Liu, Gang Guan, Guangju Stem Cell Res Ther Research BACKGROUND: Label-retaining cells (LRCs) have been recognized as rare stem and progenitor-like cells, but their complex biological features in renal repair at the cellular level have never been reported. This study was conducted to evaluate whether LRCs in kidney are indeed renal stem/progenitor cells and to delineate their potential role in kidney regeneration. METHODS: We utilized a long-term pulse chase of 5-bromo-2'-deoxyuridine (BrdU)-labeled cells in C57BL/6J mice to identify renal LRCs. We tracked the precise morphological characteristics and locations of BrdU(+)LRCs by both immunohistochemistry and immunofluorescence. To examine whether these BrdU(+)LRCs contribute to the repair of acute kidney injury, we analyzed biological characteristics of BrdU(+)LRCs in mice after ischemia/reperfusion (I/R) injury. RESULTS: The findings revealed that the nuclei of BrdU(+) LRCs exhibited different morphological characteristics in normal adult kidneys, including nuclei in pairs or scattered, fragmented or intact, strongly or weakly positive. Only 24.3 ± 1.5 % of BrdU(+) LRCs co-expressed with Ki67 and 9.1 ± 1.4 % of BrdU(+) LRCs were positive for TUNEL following renal I/R injury. Interestingly, we found that newly regenerated cells formed a niche-like structure and LRCs in pairs tended to locate in this structure, but the number of those LRCs was very low. We found a few scattered LRCs co-expressed Lotus tetragonolobus agglutinin (LTA) in the early phase of injury, suggesting differentiation of those LRCs in mouse kidney. CONCLUSIONS: Our findings suggest that LRCs are not a simple type of slow-cycling cells in adult kidneys, indicating a limited role of these cells in the regeneration of I/R injured kidney. Thus, LRCs cannot reliably be considered stem/progenitor cells in the regeneration of adult mouse kidney. When researchers use this technique to study the cellular basis of renal repair, these complex features of renal LRCs and the purity of real stem cells among renal LRCs should be considered. BioMed Central 2016-04-30 /pmc/articles/PMC4852428/ /pubmed/27137761 http://dx.doi.org/10.1186/s13287-016-0324-1 Text en © Liu et al. 2016 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 Liu, Xiangchun Liu, Haiying Sun, Lina Chen, Zhixin Nie, Huibin Sun, Aili Liu, Gang Guan, Guangju The role of long-term label-retaining cells in the regeneration of adult mouse kidney after ischemia/reperfusion injury |
title | The role of long-term label-retaining cells in the regeneration of adult mouse kidney after ischemia/reperfusion injury |
title_full | The role of long-term label-retaining cells in the regeneration of adult mouse kidney after ischemia/reperfusion injury |
title_fullStr | The role of long-term label-retaining cells in the regeneration of adult mouse kidney after ischemia/reperfusion injury |
title_full_unstemmed | The role of long-term label-retaining cells in the regeneration of adult mouse kidney after ischemia/reperfusion injury |
title_short | The role of long-term label-retaining cells in the regeneration of adult mouse kidney after ischemia/reperfusion injury |
title_sort | role of long-term label-retaining cells in the regeneration of adult mouse kidney after ischemia/reperfusion injury |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4852428/ https://www.ncbi.nlm.nih.gov/pubmed/27137761 http://dx.doi.org/10.1186/s13287-016-0324-1 |
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