中国神经再生研究(英文版) ›› 2019, Vol. 14 ›› Issue (1): 87-99.doi: 10.4103/1673-5374.243713

• 原著:神经损伤修复保护与再生 • 上一篇    下一篇

叶黄素促进神经细胞分化:基于对线粒体呼吸的调节?

  

  • 出版日期:2019-01-15 发布日期:2019-01-15

Modulation of mitochondrial respiration underpins neuronal differentiation enhanced by lutein

Kui Xie, Sherry Ngo, Jing Rong, Allan Sheppard   

  1. Liggins Institute, University of Auckland, Auckland, New Zealand
  • Online:2019-01-15 Published:2019-01-15
  • Contact: Kui Xie, PhD, k.xie@auckland.ac.nz.

摘要:

叶黄素是一种具有特殊营养价值的膳食类胡萝卜素,已显示出对视觉的有益作用;因为它优先被神经组织吸收,研究探讨了叶黄素对神经元分化的影响。结果发现叶黄素处理促进了SH-SY5Y细胞的分化,特别是增加了神经元分支和神经元标志物微管相关蛋白2(MAP2)的表达,该作用由细胞内磷酸肌醇-3-激酶(PI3K)信号传导途径介导。实验对生物能量学的分析发现,叶黄素处理增加了葡萄糖消耗,糖酵解速率和线粒体复合物的呼吸活动增强。同时,活性氧(ROS)的产生增加以及关键代谢中间体乙酰辅酶A的产生,乙酰辅酶A是细胞中表观遗传状态的重要决定因素。由此认为叶黄素刺激的神经元分化是由线粒体呼吸和信号传导的PI3K依赖性调节介导的,并且随后的代谢变化启动表观遗传学依赖的转录组重编程以支持这种形态发生。这些观察结果支持微量营养素补充剂在正常发育和再生修复过程中对神经发生的潜在重要性。

orcid: 0000-0001-7463-4047(Kui Xie)

关键词: 叶黄素, 微量营养素, 神经元分化, 代谢, PI3K-AKT途径

Abstract:

Lutein is a dietary carotenoid of particular nutritional interest as it is preferentially taken up by neural tissues. Often linked with beneficial effects on vision, a broader role for lutein in neuronal differentiation has emerged recently, although the underlying mechanisms for these effects are not yet clear. The purpose of this study was to investigate the effect of lutein on neuronal differentiation and explore the associated underpinning mechanisms. We found that lutein treatment enhanced the differentiation of SH-SY5Y cells, specifically increasing neuronal arborization and expression of the neuronal process filament protein microtubule-associated protein 2. This effect was mediated by the intracellular phosphoinositide-3-kinase (PI3K) signaling pathway. While PI3K activity is a known trigger of neuronal differentiation, more recently it has also been shown to modulate the metabolic state of cells. Our analysis of bioenergetics found that lutein treatment increased glucose consumption, rates of glycolysis and enhanced respiratory activity of mitochondrial complexes. Concomitantly, the generation of reactive oxygen species was increased (consistent with previous reports that reactive oxygen species promote neuronal differentiation), as well as the production of the key metabolic intermediate acetyl-CoA, an essential determinant of epigenetic status in the cell. We suggest that lutein-stimulated neuronal differentiation is mediated by PI3K-dependent modulation of mitochondrial respiration and signaling, and that the consequential metabolic shifts initiate epigenetically dependent transcriptomic reprogramming in support of this morphogenesis. These observations support the potential importance of micronutrients supplementation to neurogenesis, both during normal development and in regenerative repair.

Key words: lutein, micronutrient, neuronal differentiation, metabolism, PI3K-AKT pathway, glycolysis, mitochondria, gene expression