| Literature DB >> 30174297 |
Karin Golan1, Anju Kumari1, Orit Kollet1, Eman Khatib-Massalha1, Mohana Devi Subramaniam1, Zulma S Ferreira2, Francesca Avemaria1, Sylwia Rzeszotek3, Andrés García-García4, Stephanie Xie5, Eugenia Flores-Figueroa6, Shiri Gur-Cohen1, Tomer Itkin1, Aya Ludin-Tal1, Hassan Massalha7, Biana Bernshtein1, Andrzej K Ciechanowicz8, Alexander Brandis9, Tevie Mehlman9, Suditi Bhattacharya1, Mayla Bertagna1, Hui Cheng10, Ekaterina Petrovich-Kopitman9, Tomasz Janus11, Nathali Kaushansky1, Tao Cheng12, Irit Sagi13, Mariusz Z Ratajczak14, Simón Méndez-Ferrer4, John E Dick5, Regina P Markus2, Tsvee Lapidot15.
Abstract
Hematopoietic stem and progenitor cells (HSPCs) tightly couple maintenance of the bone marrow (BM) reservoir, including undifferentiated long-term repopulating hematopoietic stem cells (LT-HSCs), with intensive daily production of mature leukocytes and blood replenishment. We found two daily peaks of BM HSPC activity that are initiated by onset of light and darkness providing this coupling. Both peaks follow transient elevation of BM norepinephrine and TNF secretion, which temporarily increase HSPC reactive oxygen species (ROS) levels. Light-induced norepinephrine and TNF secretion augments HSPC differentiation and increases vascular permeability to replenish the blood. In contrast, darkness-induced TNF increases melatonin secretion to drive renewal of HSPCs and LT-HSC potential through modulating surface CD150 and c-Kit expression, increasing COX-2/αSMA+ macrophages, diminishing vascular permeability, and reducing HSPC ROS levels. These findings reveal that light- and darkness-induced daily bursts of norepinephrine, TNF, and melatonin within the BM are essential for synchronized mature blood cell production and HSPC pool repopulation.Entities:
Keywords: TNF; bone marrow; differentiation and egress; hematopoietic stem and progenitor cells; light and darkness; maintenance and retention; melatonin; norepinephrine; stem cell repopulation potential; vascular permeability
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Year: 2018 PMID: 30174297 DOI: 10.1016/j.stem.2018.08.002
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 24.633