Short-term ex-vivo exposure to hydrogen sulfide enhances murine hematopoietic stem and progenitor cell migration, homing, and proliferation
For successful transplantation of Hematopoietic Stem cells (HSCs), it is quite necessary that efficient homing, engraftment and retention of HSC self-renewal capacity takes place, which is often restricted due to inadequate number of adult HSCs. Here, we report that short-term ex-vivo treatment of m...
Main Authors: | , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Taylor & Francis Group
2020-01-01
|
Series: | Cell Adhesion & Migration |
Subjects: | |
Online Access: | http://dx.doi.org/10.1080/19336918.2020.1842131 |
id |
doaj-b38876a3fd6d48988f24a9a9be0281bc |
---|---|
record_format |
Article |
spelling |
doaj-b38876a3fd6d48988f24a9a9be0281bc2021-01-04T18:02:33ZengTaylor & Francis GroupCell Adhesion & Migration1933-69181933-69262020-01-0114121422610.1080/19336918.2020.18421311842131Short-term ex-vivo exposure to hydrogen sulfide enhances murine hematopoietic stem and progenitor cell migration, homing, and proliferationAnoushka Khanna0Namita Indracanti1Rina Chakrabarti2Prem Kumar Indraganti3Institute of Nuclear Medicine and Allied Sciences, Defence Research and Development OrganizationInstitute of Nuclear Medicine and Allied Sciences, Defence Research and Development OrganizationUniversity of DelhiInstitute of Nuclear Medicine and Allied Sciences, Defence Research and Development OrganizationFor successful transplantation of Hematopoietic Stem cells (HSCs), it is quite necessary that efficient homing, engraftment and retention of HSC self-renewal capacity takes place, which is often restricted due to inadequate number of adult HSCs. Here, we report that short-term ex-vivo treatment of mouse bone marrow mononuclear cells (BMMNCs) to Sodium Hydrogen Sulfide (NaHS, hydrogen sulfide-H2S donor) can be used as a possible strategy to overcome such hurdle. H2S increases the expression of CXCR4 on HSPCs, enhancing their migration toward SDF-1α in-vitro and thus homing to BM niche. . Additionally, in-vitro studies revealed that H2S has a role in activating mitochondria, thus, pushing quiescent HSCs into division. These results suggest a readily available and cost-effective method to facilitate efficient HSC transplantation.http://dx.doi.org/10.1080/19336918.2020.1842131stem cell migrationhomingbone marrow transplantationmitochondrial functioncxcr4 expression |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Anoushka Khanna Namita Indracanti Rina Chakrabarti Prem Kumar Indraganti |
spellingShingle |
Anoushka Khanna Namita Indracanti Rina Chakrabarti Prem Kumar Indraganti Short-term ex-vivo exposure to hydrogen sulfide enhances murine hematopoietic stem and progenitor cell migration, homing, and proliferation Cell Adhesion & Migration stem cell migration homing bone marrow transplantation mitochondrial function cxcr4 expression |
author_facet |
Anoushka Khanna Namita Indracanti Rina Chakrabarti Prem Kumar Indraganti |
author_sort |
Anoushka Khanna |
title |
Short-term ex-vivo exposure to hydrogen sulfide enhances murine hematopoietic stem and progenitor cell migration, homing, and proliferation |
title_short |
Short-term ex-vivo exposure to hydrogen sulfide enhances murine hematopoietic stem and progenitor cell migration, homing, and proliferation |
title_full |
Short-term ex-vivo exposure to hydrogen sulfide enhances murine hematopoietic stem and progenitor cell migration, homing, and proliferation |
title_fullStr |
Short-term ex-vivo exposure to hydrogen sulfide enhances murine hematopoietic stem and progenitor cell migration, homing, and proliferation |
title_full_unstemmed |
Short-term ex-vivo exposure to hydrogen sulfide enhances murine hematopoietic stem and progenitor cell migration, homing, and proliferation |
title_sort |
short-term ex-vivo exposure to hydrogen sulfide enhances murine hematopoietic stem and progenitor cell migration, homing, and proliferation |
publisher |
Taylor & Francis Group |
series |
Cell Adhesion & Migration |
issn |
1933-6918 1933-6926 |
publishDate |
2020-01-01 |
description |
For successful transplantation of Hematopoietic Stem cells (HSCs), it is quite necessary that efficient homing, engraftment and retention of HSC self-renewal capacity takes place, which is often restricted due to inadequate number of adult HSCs. Here, we report that short-term ex-vivo treatment of mouse bone marrow mononuclear cells (BMMNCs) to Sodium Hydrogen Sulfide (NaHS, hydrogen sulfide-H2S donor) can be used as a possible strategy to overcome such hurdle. H2S increases the expression of CXCR4 on HSPCs, enhancing their migration toward SDF-1α in-vitro and thus homing to BM niche. . Additionally, in-vitro studies revealed that H2S has a role in activating mitochondria, thus, pushing quiescent HSCs into division. These results suggest a readily available and cost-effective method to facilitate efficient HSC transplantation. |
topic |
stem cell migration homing bone marrow transplantation mitochondrial function cxcr4 expression |
url |
http://dx.doi.org/10.1080/19336918.2020.1842131 |
work_keys_str_mv |
AT anoushkakhanna shorttermexvivoexposuretohydrogensulfideenhancesmurinehematopoieticstemandprogenitorcellmigrationhomingandproliferation AT namitaindracanti shorttermexvivoexposuretohydrogensulfideenhancesmurinehematopoieticstemandprogenitorcellmigrationhomingandproliferation AT rinachakrabarti shorttermexvivoexposuretohydrogensulfideenhancesmurinehematopoieticstemandprogenitorcellmigrationhomingandproliferation AT premkumarindraganti shorttermexvivoexposuretohydrogensulfideenhancesmurinehematopoieticstemandprogenitorcellmigrationhomingandproliferation |
_version_ |
1724349135278047232 |