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Distinct bone marrow blood vessels differentially regulate haematopoiesis

机译:不同的骨髓血管差异调节造血功能

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摘要

Bone marrow endothelial cells (BMECs) form a network of blood vessels that regulate both leukocyte trafficking and haematopoietic stem and progenitor cell (HSPC) maintenance. However, it is not clear how BMECs balance these dual roles, and whether these events occur at the same vascular site. We found that mammalian bone marrow stem cell maintenance and leukocyte trafficking are regulated by distinct blood vessel types with different permeability properties. Less permeable arterial blood vessels maintain haematopoietic stem cells in a low reactive oxygen species (ROS) state, whereas the more permeable sinusoids promote HSPC activation and are the exclusive site for immature and mature leukocyte trafficking to and from the bone marrow. A functional consequence of high permeability of blood vessels is that exposure to blood plasma increases bone marrow HSPC ROS levels, augmenting their migration and differentiation, while compromising their long-term repopulation and survival. These findings may have relevance for clinical haematopoietic stem cell transplantation and mobilization protocols.
机译:骨髓内皮细胞(BMEC)形成血管网络,可调节白细胞运输和造血干祖细胞(HSPC)的维持。但是,尚不清楚BMEC如何平衡这些双重作用,以及这些事件是否发生在同一血管部位。我们发现,哺乳动物骨髓干细胞的维持和白细胞的运输受到具有不同渗透性的不同血管类型的调节。渗透性较差的动脉血管将造血干细胞维持在低活性氧(ROS)状态,而渗透性更强的正弦曲线可促进HSPC活化,并且是未成熟和成熟的白细胞往返骨髓运输的唯一部位。血管高通透性的功能性后果是,暴露于血浆会增加骨髓HSPC ROS水平,从而增加其迁移和分化能力,同时又会损害其长期繁殖和存活。这些发现可能与临床造血干细胞移植和动员方案有关。

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  • 来源
    《Nature》 |2016年第7599期|323-328|共6页
  • 作者单位

    Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel;

    Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel;

    Harvard Univ, Massachusetts Gen Hosp, Sch Med, Wellman Ctr Photomed, Boston, MA 02114 USA|Harvard Univ, Massachusetts Gen Hosp, Sch Med, Ctr Syst Biol, Boston, MA 02114 USA;

    Harvard Univ, Dept Stem Cell & Regenerat Biol, Cambridge, MA 02138 USA|Harvard Stem Cell Inst, Boston, MA 02114 USA|Massachusetts Gen Hosp, Ctr Regenerat Med, Boston, MA 02114 USA|Massachusetts Gen Hosp, Ctr Canc, Boston, MA 02114 USA;

    Univ Munster, Dept Tissue Morphogenesis, Max Planck Inst Mol Biomed, D-48149 Munster, Germany|Univ Munster, Fac Med, D-48149 Munster, Germany;

    Univ Munster, Dept Tissue Morphogenesis, Max Planck Inst Mol Biomed, D-48149 Munster, Germany|Univ Munster, Fac Med, D-48149 Munster, Germany;

    Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel|Tel Aviv Sourasky Med Ctr, Dept Internal Med, IL-64239 Tel Aviv, Israel;

    Harvard Univ, Massachusetts Gen Hosp, Sch Med, Wellman Ctr Photomed, Boston, MA 02114 USA|Harvard Univ, Massachusetts Gen Hosp, Sch Med, Ctr Syst Biol, Boston, MA 02114 USA;

    Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel;

    Weill Cornell Med Coll, Dept Med Genet, New York, NY 10065 USA;

    Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel;

    Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel;

    Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel;

    Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel;

    Weill Cornell Med Coll, Dept Med Genet, New York, NY 10065 USA;

    Weill Cornell Med Coll, Dept Med Genet, New York, NY 10065 USA;

    Univ Munster, Dept Tissue Morphogenesis, Max Planck Inst Mol Biomed, D-48149 Munster, Germany|Univ Munster, Fac Med, D-48149 Munster, Germany;

    Harvard Univ, Dept Stem Cell & Regenerat Biol, Cambridge, MA 02138 USA|Harvard Stem Cell Inst, Boston, MA 02114 USA|Massachusetts Gen Hosp, Ctr Regenerat Med, Boston, MA 02114 USA|Massachusetts Gen Hosp, Ctr Canc, Boston, MA 02114 USA;

    Harvard Univ, Massachusetts Gen Hosp, Sch Med, Wellman Ctr Photomed, Boston, MA 02114 USA|Harvard Univ, Massachusetts Gen Hosp, Sch Med, Ctr Syst Biol, Boston, MA 02114 USA;

    Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 02:52:10

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