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...

Full description

Bibliographic Details
Main Authors: Anoushka Khanna, Namita Indracanti, Rina Chakrabarti, Prem Kumar Indraganti
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