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Short-term ex-vivo exposure to hydrogen sulfide enhances murine hematopoietic stem and progenitor cell migration, homing, and proliferation
Cell Adhesion & Migration ( IF 3.2 ) Pub Date : 2020-11-11 , DOI: 10.1080/19336918.2020.1842131
Anoushka Khanna 1, 2 , Namita Indracanti 1 , Rina Chakrabarti 2 , Prem Kumar Indraganti 1
Affiliation  

ABSTRACT

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.



中文翻译:

短期体外暴露于硫化氢可增强小鼠造血干细胞和祖细胞的迁移、归巢和增殖

摘要

为了成功移植造血干细胞(HSC),HSC的有效归巢、植入和保留自我更新能力是非常必要的,而这往往由于成体HSC数量不足而受到限制。在此,我们报告用硫化氢钠(NaHS,硫化氢-H 2 S 供体)对小鼠骨髓单核细胞(BMMNC)进行短期离体治疗可作为克服这一障碍的可能策略。H 2 S 增加 HSPC 上 CXCR4 的表达,增强它们在体外向 SDF-1α 的迁移,从而归巢到 BM 生态位。。此外,体外研究表明,H 2 S 具有激活线粒体的作用,从而推动静止的 HSC 进入分裂。这些结果表明了一种容易获得且具有成本效益的方法来促进有效的 HSC 移植。

更新日期:2020-11-12
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