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首页> 外文期刊>Journal of Biophysical and Biochemical Cytology >De novo fatty acid synthesis by Schwann cells is essential for peripheral nervous system myelination
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De novo fatty acid synthesis by Schwann cells is essential for peripheral nervous system myelination

机译:Schwann细胞的De Novo脂肪酸合成对于外周神经系统髓鞘来说是必不可少的

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摘要

Myelination calls for a remarkable surge in cell metabolism to facilitate lipid and membrane production. Endogenous fatty acid (FA) synthesis represents a potentially critical process in myelinating glia. Using genetically modified mice, we show that Schwann cell (SC) intrinsic activity of the enzyme essential for de novo FA synthesis, fatty acid synthase (FASN), is crucial for precise lipid composition of peripheral nerves and fundamental for the correct onset of myelination and proper myelin growth. Upon FASN depletion in SCs, epineurial adipocytes undergo lipolysis, suggestive of a compensatory role. Mechanistically, we found that a lack of FASN in SCs leads to an impairment of the peroxisome proliferator-activated receptor (PPAR) γ–regulated transcriptional program. In agreement, defects in myelination of FASN-deficient SCs could be ameliorated by treatment with the PPARγ agonist rosiglitazone ex vivo and in vivo . Our results reveal that FASN-driven de novo FA synthesis in SCs is mandatory for myelination and identify lipogenic activation of the PPARγ transcriptional network as a putative downstream functional mediator.
机译:髓鞘导致细胞新陈代谢的显着浪涌,以促进脂质和膜的产生。内源性脂肪酸(FA)合成代表了髓鞘胶质胶质胶质的潜在关键方法。使用遗传修饰的小鼠,我们表明施万细胞(SC)酶的内在活性对于De Novo FA合成,脂肪酸合酶(FASN)至关重要,对外周神经的精确脂质组合和正确发作的髓鞘形成的基本脂质组合物至关重要适当的髓鞘生长。在SCS的Fasn枯竭后,髁癌脂肪细胞经历脂肪解,暗示了补偿性作用。机械地,我们发现SCS中缺乏FASN导致过氧化物体增殖物激活受体(PPAR)γ调节转录程序的损害。在一致性的情况下,通过用PPARγ激动剂Rosiglitazone离体和体内治疗可以改善Fasn缺陷SCs的髓鞘中的缺陷。我们的研究结果表明,SCS中的Fasn驱动的De Novo FA合成是髓鞘中的强制性,并鉴定PPARγ转录网络的脂原激活作为推定的下游功能介质。

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