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The nucleotide sugar UDP-glucose mobilizes long-term repopulating primitive hematopoietic cells
Sungho Kook, … , Sean Bong Lee, Byeong-Chel Lee
Sungho Kook, … , Sean Bong Lee, Byeong-Chel Lee
Published July 25, 2013
Citation Information: J Clin Invest. 2013;123(8):3420-3435. https://doi.org/10.1172/JCI64060.
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Research Article Hematology Article has an altmetric score of 11

The nucleotide sugar UDP-glucose mobilizes long-term repopulating primitive hematopoietic cells

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Abstract

Hematopoietic stem progenitor cells (HSPCs) are present in very small numbers in the circulating blood in steady-state conditions. In response to stress or injury, HSPCs are primed to migrate out of their niche to peripheral blood. Mobilized HSPCs are now commonly used as stem cell sources due to faster engraftment and reduced risk of posttransplant infection. In this study, we demonstrated that a nucleotide sugar, UDP-glucose, which is released into extracellular fluids in response to stress, mediates HSPC mobilization. UDP-glucose–mobilized cells possessed the capacity to achieve long-term repopulation in lethally irradiated animals and the ability to differentiate into multi-lineage blood cells. Compared with G-CSF–mobilized cells, UDP-glucose–mobilized cells preferentially supported long-term repopulation and exhibited lymphoid-biased differentiation, suggesting that UDP-glucose triggers the mobilization of functionally distinct subsets of HSPCs. Furthermore, co-administration of UDP-glucose and G-CSF led to greater HSPC mobilization than G-CSF alone. Administration of the antioxidant agent NAC significantly reduced UDP-glucose–induced mobilization, coinciding with a reduction in RANKL and osteoclastogenesis. These findings provide direct evidence demonstrating a potential role for UDP-glucose in HSPC mobilization and may provide an attractive strategy to improve the yield of stem cells in poor-mobilizing allogeneic or autologous donors.

Authors

Sungho Kook, Joonseok Cho, Sean Bong Lee, Byeong-Chel Lee

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Figure 3

UDP-Glc causes no significant alterations in PB wbc.

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UDP-Glc causes no significant alterations in PB wbc.
(A) B6 mice were in...
(A) B6 mice were injected as described in Figure 2A. PB mononuclear cells were collected from each treatment group and stained with indicated antibodies, followed by flow cytometry analysis. Data are depicted as the mean number of wbc per milliliter of blood. For lineage marker–expressing cells, a mean value of the cell number ± SD obtained from 3 independent experiments is shown. (B) Csf3r–/– (KO) and WT mice were treated with UDP-Glc or PBS as described above. n > 5 mice/group. Left: Flow cytometry plots show the gating strategy for identification of LSK cells. PB cells were gated on a forward-scatter/side-scatter (FS/SS) dot plot. Lin– cells were gated (data not shown), with subsequent gating on c-Kit+Sca-1+ cells. Right: Mice (n > 5/group) were individually analyzed for each group. (C) Csf3r–/– (KO) and WT mice (n = 5/group) were treated as described above. PB was collected and analyzed as described in A. Data are mean ± SD of 3 independent experiments (A and C). *P < 0.05, **P < 0.01; ##P < 0.01 vs. Csfr+/+ CTL.

Copyright © 2025 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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