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Leptin Receptor Promotes Adipogenesis and Reduces Osteogenesis by Regulating Mesenchymal Stromal Cells in Adult Bone Marrow

机译:瘦素受体通过调节成年骨髓中的间质基质细胞促进脂肪形成和减少成骨

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Skeletal stem cells (SSCs) that are the major source of osteoblasts and adipocytes in adult bone marrow express leptin receptor (LepR). To test whether LepR regulates SSC function, we conditionally deleted Lepr from limb bone marrow stromal cells, but not from the axial skeleton or hypothalamic neurons, using Prx1-Cre. Prx1-Cre;Lepr(fl/fl) mice exhibited normal body mass and normal hematopoiesis. However, limb bones from Prx1-Cre;Lepr(fl/fl) mice exhibited increased osteogenesis, decreased adipogenesis, and accelerated fracture healing. Leptin increased adipogenesis and reduced osteogenesis by activating Jak2/Stat3 signaling in bone marrow stromal cells. A high-fat diet increased adipogenesis and reduced osteogenesis in limb bones from wild-type mice, but not from Prx1-Cre;Lepr(fl/fl) mice. This reflected local effects of LepR on osteogenesis and adipogenesis by bone marrow stromal cells and systemic effects on bone resorption. Leptin/LepR signaling regulates adipogenesis and osteogenesis by mesenchymal stromal cells in the bone marrow in response to diet and adiposity.
机译:骨骼干细胞(SSC)是成年骨髓中成骨细胞和脂肪细胞的主要来源,它表达瘦素受体(LepR)。为了测试LepR是否调节SSC功能,我们使用Prx1-Cre有条件地从肢体骨髓基质细胞中删除了Lepr,但没有从轴向骨骼或下丘脑神经元中删除。 Prx1-Cre; Lepr(fl / fl)小鼠表现出正常的体重和正常的造血作用。但是,Prx1-Cre; Lepr(fl / fl)小鼠的四肢骨骼显示出增加的成骨作用,减少的脂肪形成和加速的骨折愈合。瘦素通过激活骨髓基质细胞中的Jak2 / Stat3信号传导来增加脂肪生成并减少成骨作用。高脂饮食可增加野生型小鼠肢体骨骼的脂肪生成并减少成骨,但Prx1-Cre; Lepr(fl / fl)小鼠则不然。这反映了LepR对骨髓基质细胞成骨和成脂的局部作用以及对骨吸收的全身作用。瘦素/ LepR信号传导通过饮食中的脂肪和肥胖调节骨髓间充质基质细胞的脂肪形成和成骨作用。

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