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首页> 外文期刊>Journal of cell biology >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:雪旺细胞从头合成脂肪酸对周围神经系统髓鞘形成至关重要

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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:髓鞘化要求细胞代谢显着增加,以促进脂质和膜的产生。内源性脂肪酸(FA)的合成代表了髓鞘神经胶质的潜在关键过程。使用转基因小鼠,我们显示出从头FA合成所必需的酶Schwann细胞(SC)的内在活性,脂肪酸合酶(FASN),对于周围神经的精确脂质组成至关重要,对于髓鞘形成的正确发作至关重要。适当的髓磷脂生长。在SCs中FASN耗尽后,肾上腺脂肪细胞发生脂解,提示其具有补偿作用。从机制上讲,我们发现SC中FASN的缺乏会导致过氧化物酶体增殖物激活受体(PPAR)γ调控的转录程序的损害。一致地,可以通过离体和体内用PPARγ激动剂罗格列酮治疗来改善FASN缺陷型SCs的髓鞘化缺陷。我们的研究结果表明,SCs中FASN驱动的从头FA合成对于髓鞘化是必不可少的,并且可以将PPARγ转录网络的脂肪生成激活作为假定的下游功能介体。

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