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Enhancing Hematopoietic Stem Cell Transplantation Efficacy by Mitigating Oxygen Shock

机译:通过减轻氧气冲击来增强造血干细胞移植的功效

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Hematopoietic stem cells (HSCs) reside in hypoxic niches within bone marrow and cord blood. Yet, essentially all HSC studies have been performed with cells isolated and processed in non-physiologic ambient air. By collecting and manipulating bone marrow and cord blood in native conditions of hypoxia, we demonstrate that brief exposure to ambient oxygen decreases recovery of long-term repopulating HSCs and increases progenitor cells, a phenomenon we term extraphysiologic oxygen shock/stress (EPHOSS). Thus, true numbers of HSCs in the bone marrow and cord blood are routinely underestimated. We linked ROS production and induction of the mitochondrial permeability transition pore (MPTP) via cyclophilin D and p53 as mechanisms of EPHOSS. The MPTP inhibitor cyclosporin A protects mouse bone marrow and human cord blood HSCs from EPHOSS during collection in air, resulting in increased recovery of transplantable HSCs. Mitigating EPHOSS during cell collection and processing by pharmacological means may be clinically advantageous for transplantation.
机译:造血干细胞(HSC)驻留在骨髓和脐带血中的低氧环境中。但是,基本上所有的HSC研究都是在非生理环境空气中分离并处理过的细胞中进行的。通过在缺氧的自然条件下收集和处理骨髓和脐带血,我们证明了短暂暴露于环境氧会降低长期繁殖的HSC的恢复并增加祖细胞,这种现象我们称为生理外氧休克/压力(EPHOSS)。因此,通常会低估骨髓和脐带血中HSC的真实数量。我们通过亲环蛋白D和p53将ROS的产生和线粒体通透性转换孔(MPTP)的诱导作为EPHOSS的机制。 MPTP抑制剂环孢菌素A在空气中收集期间可保护小鼠骨髓和人脐血HSC免受EPHOSS侵害,从而提高了可移植HSC的回收率。通过药理学方法减轻细胞收集和加工过程中的EPHOSS在临床上对于移植可能是有利的。

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