虾青素在秀丽隐杆线虫自噬中延长寿命的作用。

IF 2.2 4区 医学 Q3 GERIATRICS & GERONTOLOGY
Rejuvenation research Pub Date : 2021-06-01 Epub Date: 2020-11-30 DOI:10.1089/rej.2020.2355
Min Fu, Xumei Zhang, Xuguang Zhang, Liu Yang, Suhui Luo, Huan Liu
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引用次数: 13

摘要

虾青素(AST)是一种叶黄素,属于类胡萝卜素家族,是一种有效的抗氧化剂。AST对长寿的影响及其生理分子机制尚不清楚。在本研究中,我们证明了AST可以延长秀丽隐杆线虫的寿命。为了揭示AST是否可以通过上调自噬来延缓衰老,我们测量了自噬基因bec1突变体线虫的自噬基因表达和寿命,结果显示AST干预后自噬基因表达上调,bec1的破坏削弱了寿命的延长。为探究ast诱导自噬上调的分子机制,我们通过RNA干扰敲除胰岛素/胰岛素生长因子-1 [IGF-1]信号通路或雷帕霉素[TOR]信号通路关键基因daf-16或hlh-30,自噬基因lgg-1表达降低。综上所述,我们的研究结果强烈提示,依赖于胰岛素/IGF-1信号通路和TOR信号通路的自噬作用通过AST延长秀丽隐杆线虫的寿命。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Autophagy Plays a Role in the Prolongation of the Life Span of Caenorhabditis elegans by Astaxanthin.

Astaxanthin (AST), a xanthophyll belonging to the family of carotenoids, is a potent antioxidant. The effect of AST on longevity and its physiological and molecular mechanism are still unclear. In this study, we proved that AST could prolong the life span of Caenorhabditis elegans. To uncover whether AST could delay aging by upregulating autophagy, we measured the expression of autophagy gene and the life span of autophagy gene bec-1 mutant nematodes, and the results showed that the expression of autophagy gene was upregulated after AST intervention and the disruption of bec-1 weakened the extension of the life span. To explore the molecular mechanism of AST-induced autophagy upregulation, we knocked out the daf-16 or hlh-30 (key genes of insulin/insulin growth factor-1 [IGF-1] signal pathway or target of rapamycin [TOR] signal pathway) by RNA interference, and the expression of autophagy gene lgg-1 decreased. Collectively, our results strongly suggest that autophagy, which is both the insulin/IGF-1 signal pathway dependent and TOR signal pathway dependent, plays a role in the prolongation of the life span of Caenorhabditis elegans by AST.

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来源期刊
Rejuvenation research
Rejuvenation research 医学-老年医学
CiteScore
4.50
自引率
0.00%
发文量
41
审稿时长
3 months
期刊介绍: Rejuvenation Research publishes cutting-edge, peer-reviewed research on rejuvenation therapies in the laboratory and the clinic. The Journal focuses on key explorations and advances that may ultimately contribute to slowing or reversing the aging process, and covers topics such as cardiovascular aging, DNA damage and repair, cloning, and cell immortalization and senescence. Rejuvenation Research coverage includes: Cell immortalization and senescence Pluripotent stem cells DNA damage/repair Gene targeting, gene therapy, and genomics Growth factors and nutrient supply/sensing Immunosenescence Comparative biology of aging Tissue engineering Late-life pathologies (cardiovascular, neurodegenerative and others) Public policy and social context.
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