Distinct bone marrow blood vessels differentially regulate haematopoiesis

被引:0
|
作者
Tomer Itkin
Shiri Gur-Cohen
Joel A. Spencer
Amir Schajnovitz
Saravana K. Ramasamy
Anjali P. Kusumbe
Guy Ledergor
Yookyung Jung
Idan Milo
Michael G. Poulos
Alexander Kalinkovich
Aya Ludin
Karin Golan
Eman Khatib
Anju Kumari
Orit Kollet
Guy Shakhar
Jason M. Butler
Shahin Rafii
Ralf H. Adams
David T. Scadden
Charles P. Lin
Tsvee Lapidot
机构
[1] The Weizmann Institute of Science,Department of Immunology
[2] Wellman Center for Photomedicine,Department of Stem Cell and Regenerative Biology
[3] Massachusetts General Hospital,Department of Tissue Morphogenesis and Faculty of Medicine
[4] Harvard Medical School,Internal Medicine Department
[5] Center for Systems Biology,Department of Genetic Medicine
[6] Massachusetts General Hospital,undefined
[7] Harvard Medical School,undefined
[8] Harvard University,undefined
[9] Harvard Stem Cell Institute,undefined
[10] Center for Regenerative Medicine and Cancer Center,undefined
[11] Massachusetts General Hospital,undefined
[12] Max Planck Institute for Molecular Biomedicine,undefined
[13] University of Münster,undefined
[14] Tel-Aviv Sourasky Medical Center,undefined
[15] Weill Cornell Medical College,undefined
来源
Nature | 2016年 / 532卷
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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.
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页码:323 / 328
页数:5
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