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长链脂肪酸氧化障碍患者成纤维细胞中偶数和奇数中链脂肪酸引起的脂质组学和蛋白质组学改变。

Lipidomic and Proteomic Alterations Induced by Even and Odd Medium-Chain Fatty Acids on Fibroblasts of Long-Chain Fatty Acid Oxidation Disorders.

机构信息

Department of General Pediatrics, Adolescent Medicine and Neonatology, Faculty of Medicine, Medical Centre-University of Freiburg, 79106 Freiburg, Germany.

Faculty of Biology, University of Freiburg, 79104 Freiburg, Germany.

出版信息

Int J Mol Sci. 2021 Sep 29;22(19):10556. doi: 10.3390/ijms221910556.

Abstract

Medium-chain fatty acids (mc-FAs) are currently applied in the treatment of long-chain fatty acid oxidation disorders (lc-FAOD) characterized by impaired β-oxidation. Here, we performed lipidomic and proteomic analysis in fibroblasts from patients with very long-chain acyl-CoA dehydrogenase (VLCADD) and long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHADD) deficiencies after incubation with heptanoate (C7) and octanoate (C8). Defects of β-oxidation induced striking proteomic alterations, whereas the effect of treatment with mc-FAs was minor. However, mc-FAs induced a remodeling of complex lipids. Especially C7 appeared to act protectively by restoring sphingolipid biosynthesis flux and improving the observed dysregulation of protein homeostasis in LCHADD under control conditions.

摘要

中链脂肪酸(mc-FAs)目前被应用于长链脂肪酸氧化障碍(lc-FAOD)的治疗中,这些障碍的特征是β-氧化受损。在这里,我们对长链酰基辅酶 A 脱氢酶(VLCADD)和长链 3-羟基酰基辅酶 A 脱氢酶(LCHADD)缺乏症患者的成纤维细胞进行了脂组学和蛋白质组学分析,这些细胞在孵育庚酸(C7)和辛酸(C8)后。β-氧化缺陷引起了明显的蛋白质组学改变,而 mc-FAs 的治疗效果则较小。然而,mc-FAs 诱导了复杂脂质的重塑。特别是 C7 似乎通过恢复神经酰胺生物合成通量和改善 LCHADD 在对照条件下观察到的蛋白质平衡失调发挥了保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/276a/8508682/1b875a8da441/ijms-22-10556-g001.jpg

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