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肥胖小鼠的微生物群通过改变骨髓微环境来调节造血干细胞分化。

Microbiota from Obese Mice Regulate Hematopoietic Stem Cell Differentiation by Altering the Bone Niche.

机构信息

Department of Internal Medicine 3, University of Erlangen-Nuremberg, Erlangen 91054, Germany.

Department of Radiology, Preclinical Imaging, University of Erlangen-Nuremberg, Erlangen 91054, Germany.

出版信息

Cell Metab. 2015 Nov 3;22(5):886-94. doi: 10.1016/j.cmet.2015.08.020. Epub 2015 Sep 17.

Abstract

The effect of metabolic stress on the bone marrow microenvironment is poorly defined. We show that high-fat diet (HFD) decreased long-term Lin(-)Sca-1(+)c-Kit(+) (LSK) stem cells and shifted lymphoid to myeloid cell differentiation. Bone marrow niche function was impaired after HFD as shown by poor reconstitution of hematopoietic stem cells. HFD led to robust activation of PPARγ2, which impaired osteoblastogenesis while enhancing bone marrow adipogenesis. At the same time, expression of genes such as Jag-1, SDF-1, and IL-7 forming the bone marrow niche was highly suppressed after HFD. Moreover, structural changes of microbiota were associated to HFD-induced bone marrow changes. Antibiotic treatment partially rescued HFD-mediated effects on the bone marrow niche, while transplantation of stools from HFD mice could transfer the effect to normal mice. These findings show that metabolic stress affects the bone marrow niche by alterations of gut microbiota and osteoblast-adipocyte homeostasis.

摘要

代谢应激对骨髓微环境的影响还不甚明确。我们发现高脂饮食(HFD)会减少长期 Lin(-)Sca-1(+)c-Kit(+)(LSK)干细胞,并促使淋系细胞向髓系细胞分化。HFD 后骨髓龛功能受损,造血干细胞的重建能力下降。HFD 导致 PPARγ2 的强烈激活,损害成骨细胞生成,同时增强骨髓脂肪生成。与此同时,Jag-1、SDF-1 和 IL-7 等形成骨髓龛的基因的表达在 HFD 后受到高度抑制。此外,肠道微生物组的结构变化与 HFD 引起的骨髓变化有关。抗生素治疗部分挽救了 HFD 对骨髓龛的影响,而 HFD 小鼠的粪便移植可将该影响转移至正常小鼠。这些发现表明,代谢应激通过改变肠道微生物组和骨细胞-脂肪细胞平衡来影响骨髓龛。

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