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  1. Article ; Online: Dynamic Cross Talk between S1P and CXCL12 Regulates Hematopoietic Stem Cells Migration, Development and Bone Remodeling

    Karin Golan / Orit Kollet / Tsvee Lapidot

    Pharmaceuticals, Vol 6, Iss 9, Pp 1145-

    2013  Volume 1169

    Abstract: Hematopoietic stem cells (HSCs) are mostly retained in a quiescent non-motile mode in their bone marrow (BM) niches, shifting to a migratory cycling and differentiating state to replenish the blood with mature leukocytes on demand. The balance between ... ...

    Abstract Hematopoietic stem cells (HSCs) are mostly retained in a quiescent non-motile mode in their bone marrow (BM) niches, shifting to a migratory cycling and differentiating state to replenish the blood with mature leukocytes on demand. The balance between the major chemo-attractants CXCL12, predominantly in the BM, and S1P, mainly in the blood, dynamically regulates HSC recruitment to the circulation versus their retention in the BM. During alarm situations, stress-signals induce a decrease in CXCL12 levels in the BM, while S1P levels are rapidly and transiently increased in the circulation, thus favoring mobilization of stem cells as part of host defense and repair mechanisms. Myeloid cytokines, including G-CSF, up-regulate S1P signaling in the BM via the PI3K pathway. Induced CXCL12 secretion from stromal cells via reactive oxygen species (ROS) generation and increased S1P1 expression and ROS signaling in HSCs, all facilitate mobilization. Bone turnover is also modulated by both CXCL12 and S1P, regulating the dynamic BM stromal microenvironment, osteoclasts and stem cell niches which all functionally express CXCL12 and S1P receptors. Overall, CXCL12 and S1P levels in the BM and circulation are synchronized to mutually control HSC motility, leukocyte production and osteoclast/osteoblast bone turnover during homeostasis and stress situations.
    Keywords hematopoietic stem cells ; CXCL12/CXCR4 ; S1P ; mobilization ; bone remodeling ; Medicine ; R ; Pharmacy and materia medica ; RS1-441
    Subject code 572
    Language English
    Publishing date 2013-09-01T00:00:00Z
    Publisher MDPI AG
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  2. Article ; Online: Lactate released by inflammatory bone marrow neutrophils induces their mobilization via endothelial GPR81 signaling

    Eman Khatib-Massalha / Suditi Bhattacharya / Hassan Massalha / Adi Biram / Karin Golan / Orit Kollet / Anju Kumari / Francesca Avemaria / Ekaterina Petrovich-Kopitman / Shiri Gur-Cohen / Tomer Itkin / Isabell Brandenburger / Asaf Spiegel / Ziv Shulman / Zachary Gerhart-Hines / Shalev Itzkovitz / Matthias Gunzer / Stefan Offermanns / Ronen Alon /
    Amiram Ariel / Tsvee Lapidot

    Nature Communications, Vol 11, Iss 1, Pp 1-

    2020  Volume 18

    Abstract: Lactate is a by-product of glycolysis that can function via its G protein receptor GPR81. Here the authors show that LPS or Salmonella infection enhances glycolytic metabolism in bone marrow neutrophils, resulting in lactate production, which increases ... ...

    Abstract Lactate is a by-product of glycolysis that can function via its G protein receptor GPR81. Here the authors show that LPS or Salmonella infection enhances glycolytic metabolism in bone marrow neutrophils, resulting in lactate production, which increases endothelial barrier permeability and mobilization of these neutrophils by targeting endothelial GPR81.
    Keywords Science ; Q
    Language English
    Publishing date 2020-07-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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