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Saturated fatty acids enhance osteoclast survival.

机译:饱和脂肪酸可提高破骨细胞的存活率。

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Hyperlipidemia and marrow fat are associated with lowering bone density in vivo, suggesting that lipid contributes to bone loss. Using bone marrow-derived macrophages, we investigated the effect of saturated fatty acids (SFA) on osteoclastogenesis. The level of free fatty acids and adiposity in bone marrow was significantly elevated in obese mice. SFA increased osteoclast (OC) survival by preventing apoptosis. SFA caused the production of MIP-1alpha and led to activation of nuclear factor (NF)-kappaB in the OC. The absence of Toll-like receptor 4 (TLR4) or myeloid differentiation factor 88 (MyD88) abolished the survival effect of SFA on OC.
机译:高脂血症和骨髓脂肪与体内体内骨密度降低有关,提示脂质有助于骨质流失。使用骨髓来源的巨噬细胞,我们调查了饱和脂肪酸(SFA)对破骨细胞形成的影响。肥胖小鼠的骨髓中游离脂肪酸和脂肪水平显着升高。 SFA通过防止细胞凋亡增加破骨细胞(OC)的存活率。 SFA导致MIP-1alpha的产生并导致OC中核因子(NF)-κB的活化。 Toll样受体4(TLR4)或髓系分化因子88(MyD88)的缺乏消除了SFA对OC的存活作用。

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