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Nitric oxide has contrasting age-dependent effects on the functionality of murine hematopoietic stem cells

BACKGROUND: The success of hematopoietic stem cell (HSC) transplantation is dependent on the quality of the donor HSCs. Some sources of HSCs display reduced engraftment efficiency either because of inadequate number (e.g., fetal liver and cord blood), or age-related dysfunction (e.g. in older indivi...

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Autores principales: Jalnapurkar, Sapana, Singh, Shweta, Devi, Moirangthem Ranjita, Limaye, Lalita, Kale, Vaijayanti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5120451/
https://www.ncbi.nlm.nih.gov/pubmed/27876094
http://dx.doi.org/10.1186/s13287-016-0433-x
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author Jalnapurkar, Sapana
Singh, Shweta
Devi, Moirangthem Ranjita
Limaye, Lalita
Kale, Vaijayanti
author_facet Jalnapurkar, Sapana
Singh, Shweta
Devi, Moirangthem Ranjita
Limaye, Lalita
Kale, Vaijayanti
author_sort Jalnapurkar, Sapana
collection PubMed
description BACKGROUND: The success of hematopoietic stem cell (HSC) transplantation is dependent on the quality of the donor HSCs. Some sources of HSCs display reduced engraftment efficiency either because of inadequate number (e.g., fetal liver and cord blood), or age-related dysfunction (e.g. in older individuals). Therefore, use of pharmacological compounds to improve functionality of HSCs is a forefront research area in hematology. METHODS: Lineage negative (Lin(−)) cells isolated from murine bone marrow or sort-purified Lin(−)Sca-1(+)c-Kit(+)CD34(−) (LSK-CD34(−)) were treated with a nitric oxide donor, sodium nitroprusside (SNP). The cells were subjected to various phenotypic and functional assays. RESULTS: We found that SNP treatment of Lin(−) cells leads to an increase in the numbers of LSK-CD34(+) cells in them. Using sort-purified LSK CD34(−) HSCs, we show that this is related to acquisition of CD34 expression by LSK-CD34(−) cells, rather than proliferation of LSK-CD34(+) cells. Most importantly, this upregulated expression of CD34 had age-dependent contrasting effects on HSC functionality. Increased CD34 expression significantly improved the engraftment of juvenile HSCs (6–8 weeks); in sharp contrast, it reduced the engraftment of adult HSCs (10–12 weeks). The molecular mechanism behind this phenomenon involved nitric oxide (NO)-mediated differential induction of various transcription factors involved in commitment with regard to self-renewal in adult and juvenile HSCs, respectively. Preliminary experiments performed on cord blood-derived and mobilized peripheral blood-derived cells revealed that NO exerts age-dependent contrasting effects on human HSCs as well. CONCLUSIONS: This study demonstrates novel age-dependent contrasting effects of NO on HSC functionality and suggests that HSC age may be an important parameter in screening of various compounds for their use in manipulation of HSCs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13287-016-0433-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-51204512016-11-28 Nitric oxide has contrasting age-dependent effects on the functionality of murine hematopoietic stem cells Jalnapurkar, Sapana Singh, Shweta Devi, Moirangthem Ranjita Limaye, Lalita Kale, Vaijayanti Stem Cell Res Ther Research BACKGROUND: The success of hematopoietic stem cell (HSC) transplantation is dependent on the quality of the donor HSCs. Some sources of HSCs display reduced engraftment efficiency either because of inadequate number (e.g., fetal liver and cord blood), or age-related dysfunction (e.g. in older individuals). Therefore, use of pharmacological compounds to improve functionality of HSCs is a forefront research area in hematology. METHODS: Lineage negative (Lin(−)) cells isolated from murine bone marrow or sort-purified Lin(−)Sca-1(+)c-Kit(+)CD34(−) (LSK-CD34(−)) were treated with a nitric oxide donor, sodium nitroprusside (SNP). The cells were subjected to various phenotypic and functional assays. RESULTS: We found that SNP treatment of Lin(−) cells leads to an increase in the numbers of LSK-CD34(+) cells in them. Using sort-purified LSK CD34(−) HSCs, we show that this is related to acquisition of CD34 expression by LSK-CD34(−) cells, rather than proliferation of LSK-CD34(+) cells. Most importantly, this upregulated expression of CD34 had age-dependent contrasting effects on HSC functionality. Increased CD34 expression significantly improved the engraftment of juvenile HSCs (6–8 weeks); in sharp contrast, it reduced the engraftment of adult HSCs (10–12 weeks). The molecular mechanism behind this phenomenon involved nitric oxide (NO)-mediated differential induction of various transcription factors involved in commitment with regard to self-renewal in adult and juvenile HSCs, respectively. Preliminary experiments performed on cord blood-derived and mobilized peripheral blood-derived cells revealed that NO exerts age-dependent contrasting effects on human HSCs as well. CONCLUSIONS: This study demonstrates novel age-dependent contrasting effects of NO on HSC functionality and suggests that HSC age may be an important parameter in screening of various compounds for their use in manipulation of HSCs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13287-016-0433-x) contains supplementary material, which is available to authorized users. BioMed Central 2016-11-22 /pmc/articles/PMC5120451/ /pubmed/27876094 http://dx.doi.org/10.1186/s13287-016-0433-x Text en © The Author(s). 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
Jalnapurkar, Sapana
Singh, Shweta
Devi, Moirangthem Ranjita
Limaye, Lalita
Kale, Vaijayanti
Nitric oxide has contrasting age-dependent effects on the functionality of murine hematopoietic stem cells
title Nitric oxide has contrasting age-dependent effects on the functionality of murine hematopoietic stem cells
title_full Nitric oxide has contrasting age-dependent effects on the functionality of murine hematopoietic stem cells
title_fullStr Nitric oxide has contrasting age-dependent effects on the functionality of murine hematopoietic stem cells
title_full_unstemmed Nitric oxide has contrasting age-dependent effects on the functionality of murine hematopoietic stem cells
title_short Nitric oxide has contrasting age-dependent effects on the functionality of murine hematopoietic stem cells
title_sort nitric oxide has contrasting age-dependent effects on the functionality of murine hematopoietic stem cells
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5120451/
https://www.ncbi.nlm.nih.gov/pubmed/27876094
http://dx.doi.org/10.1186/s13287-016-0433-x
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