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27-Hydroxycholesterol induces hematopoietic stem cell mobilization and extramedullary hematopoiesis during pregnancy
Hideyuki Oguro, … , Philip W. Shaul, Sean J. Morrison
Hideyuki Oguro, … , Philip W. Shaul, Sean J. Morrison
Published August 7, 2017
Citation Information: J Clin Invest. 2017;127(9):3392-3401. https://doi.org/10.1172/JCI94027.
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Research Article

27-Hydroxycholesterol induces hematopoietic stem cell mobilization and extramedullary hematopoiesis during pregnancy

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Abstract

Extramedullary hematopoiesis (EMH) is induced during pregnancy to support rapid expansion of maternal blood volume. EMH activation requires hematopoietic stem cell (HSC) proliferation and mobilization, processes that depend upon estrogen receptor α (ERα) in HSCs. Here we show that treating mice with estradiol to model estradiol increases during pregnancy induced HSC proliferation in the bone marrow but not HSC mobilization. Treatment with the alternative ERα ligand 27-hydroxycholesterol (27HC) induced ERα-dependent HSC mobilization and EMH but not HSC division in the bone marrow. During pregnancy, 27HC levels increased in hematopoietic stem/progenitor cells as a result of CYP27A1, a cholesterol hydroxylase. Cyp27a1-deficient mice had significantly reduced 27HC levels, HSC mobilization, and EMH during pregnancy but normal bone marrow hematopoiesis and EMH in response to bleeding or G-CSF treatment. Distinct hematopoietic stresses thus induce EMH through different mechanisms. Two different ERα ligands, estradiol and 27HC, work together to promote EMH during pregnancy, revealing a collaboration of hormonal and metabolic mechanisms as well as a physiological function for 27HC in normal mice.

Authors

Hideyuki Oguro, Jeffrey G. McDonald, Zhiyu Zhao, Michihisa Umetani, Philip W. Shaul, Sean J. Morrison

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Figure 2

27HC-induced mobilization of hematopoietic stem and progenitor cells requires Esr1 but not Csf3.

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27HC-induced mobilization of hematopoietic stem and progenitor cells req...
(A) Representative spleen sections stained with H&E from mice treated with vehicle (left) or 27HC (right) daily for 6 days. Lower-magnification (top) and higher-magnification (bottom) images are shown. Scale bars: 200 μm (top panels); 50 μm (bottom panels). (B and C) The numbers of hematopoietic stem and progenitor cells in the bone marrow (femurs and tibias; B) and spleen (C) of Csf3+/+ or Csf3–/– mice treated with vehicle or 27HC daily for 6 days (a total of 5 mice/treatment from 4 independent experiments). (D) Numbers of CFU in the blood of mice treated with vehicle, 27HC, G-CSF, or a combination of 27HC and G-CSF daily for 6 days (a total of 4–6 mice/treatment from 6 independent experiments). (E and F) Numbers of hematopoietic stem and progenitor cells in the bone marrow (femurs and tibias; E) and spleen (F) of Vav1-icre; Esr1fl/fl mice or Esr1fl/fl controls treated with vehicle or 27HC daily for 6 days (a total of 3 mice/treatment from 3 independent experiments). Statistical significance was assessed using 1-way ANOVA with Šídák’s multiple comparisons tests (*P < 0.05, ‡P < 0.01, #P < 0.001). All data represent mean ± SD.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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