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LECT2 drives haematopoietic stem cell expansion and mobilization via regulating the macrophages and osteolineage cells

机译:LECT2通过调节巨噬细胞和骨系细胞来驱动造血干细胞的扩增和动员

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摘要

Haematopoietic stem cells (HSCs) can differentiate into cells of all lineages in the blood. However, the mechanisms by which cytokines in the blood affect HSC homeostasis remain largely unknown. Here we show that leukocyte cell-derived chemotaxin 2 (LECT2), a multifunctional cytokine, induces HSC expansion and mobilization. Recombinant LECT2 administration results in HSC expansion in the bone marrow and mobilization to the blood via CD209a. The effect of LECT2 on HSCs is reduced after specific depletion of macrophages or reduction of osteolineage cells. LECT2 treatment reduces the tumour necrosis factor (TNF) expression in macrophages and osteolineage cells. In TNF knockout mice, the effect of LECT2 on HSCs is reduced. Moreover, LECT2 induces HSC mobilization in irradiated mice, while granulocyte colony-stimulating factor does not. Our results illustrate that LECT2 is an extramedullar cytokine that contributes to HSC homeostasis and may be useful to induce HSC mobilization.
机译:造血干细胞(HSC)可以分化为血液中所有谱系的细胞。然而,血液中细胞因子影响HSC稳态的机制仍然未知。在这里,我们显示白细胞衍生的趋化因子2(LECT2),一种多功能的细胞因子,诱导HSC扩展和动员。重组LECT2给药导致HSC在骨髓中扩增,并通过CD209a动员到血液中。 LECT2对HSC的作用在巨噬细胞特异性消耗或骨系细胞减少后降低。 LECT2处理可降低巨噬细胞和骨系细胞中的肿瘤坏死因子(TNF)表达。在TNF基因敲除小鼠中,LECT2对HSC的作用降低。此外,LECT2诱导辐照小鼠的HSC动员,而粒细胞集落刺激因子则不然。我们的结果表明,LECT2是一种髓外细胞因子,可促进HSC的稳态,可能有助于诱导HSC的动员。

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