Neomangiferin prolongs the lifespan of Caenorhabditis elegans by regulating autophagy-dependent IIS and MAPK pathways via bas-1

秀丽隐杆线虫 MAPK/ERK通路 细胞生物学 自噬 脂褐素 生物 信号转导 转录因子 活性氧 p38丝裂原活化蛋白激酶 氧化应激 小桶 下调和上调 蛋白激酶A 化学 生物化学 突变体 激酶 磷脂过氧化氢谷胱甘肽过氧化物酶 磷酸化 KEAP1型 Wnt信号通路 亚细胞定位 PI3K/AKT/mTOR通路 抗氧化剂 刺猬信号通路 转录组 姜黄素
作者
Mei Wu,Feng Qiu,Dandan Li,Yiming Zhou,Lijuan Chen,Wei He,Nuokun Li,Xiaodan Liu,Meijing Wang,Mengting Zhang,Li Gong,Wei Bin Fang,Meng Pan
出处
期刊:Food & Function [Royal Society of Chemistry]
卷期号:16 (19): 7690-7704 被引量:2
标识
DOI:10.1039/d5fo02007g
摘要

Neomangiferin (NG) is an active ingredient extracted from mango, recognized for its antioxidant potential. However, its anti-aging efficacy remains largely unexplored. This study employed Caenorhabditis elegans (C. elegans) to evaluate the anti-aging activity of NG and investigate the corresponding molecular mechanism. Our findings demonstrated that NG significantly extended the average lifespan of C. elegans, by reducing the levels of lipofuscin and reactive oxygen species (ROS), as well as improving the survival rate under heat stress, oxidative stress, and UV stress. Transcriptomics results identified bas-1-a pivotal gene governing dopamine biosynthesis-as the most significantly upregulated target, with KEGG pathway enrichment highlighting coordinated activation of autophagy systems, insulin/insulin-like growth factor signaling (IIS) pathways, and mitogen-activated protein kinase (MAPK) cascades. Subsequent qPCR and other experiments verify that NG significantly upregulates bas-1, IIS pathways (daf-16, sod-3, and ctl-1), MAPK pathways (sek-1, pmk-1, skn-1, gcs-1, and gst-4), and autophagy pathways (lgg-1 and sqst-1), and significantly increases the number of lgg-1::GFP puncta. Mechanistically, fluorescence localization assays confirmed that NG promotes nuclear translocation of daf-16 and skn-1, while genetic ablation of these transcription factors inhibited NG-mediated ROS reduction, stress resilience and lipofuscin levels. Moreover, the molecular docking results showed that NG binds to bas-1 through hydrogen bonding interactions, hydrophobic interactions and salt bridge interactions. Critically, the bas-1 mutant exhibited substantially attenuated activation of autophagy as well as the IIS and MAPK pathways, ultimately weakening NG-mediated autophagy and anti-aging efficacy. Therefore, the targeted upregulation of bas-1 by NG through activating autophagy may potentially represent a novel and promising approach for alleviating aging.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
CipherSage应助落后芷文采纳,获得30
1秒前
王子熙发布了新的文献求助10
1秒前
2秒前
2秒前
栗松琛完成签到,获得积分20
3秒前
明理道之完成签到,获得积分10
4秒前
乐乐应助Eternity采纳,获得10
4秒前
lauren发布了新的文献求助10
4秒前
5秒前
红丿丿发布了新的文献求助10
6秒前
栗松琛发布了新的文献求助10
7秒前
7秒前
8秒前
ccc发布了新的文献求助10
11秒前
congcong成协完成签到,获得积分10
11秒前
12秒前
14秒前
陈蔡宇完成签到,获得积分10
16秒前
上官若男应助Sene采纳,获得10
16秒前
18秒前
20秒前
22秒前
万能图书馆应助iligll采纳,获得10
22秒前
微笑千愁完成签到 ,获得积分10
23秒前
舒心的飞荷完成签到 ,获得积分10
24秒前
科研通AI6.2应助zhengtan采纳,获得10
24秒前
25秒前
菠萝完成签到 ,获得积分0
26秒前
26秒前
28秒前
29秒前
张辰熙完成签到 ,获得积分10
30秒前
色彩发布了新的文献求助10
30秒前
潇洒的绮山完成签到,获得积分10
31秒前
32秒前
Bethune124完成签到 ,获得积分10
33秒前
还差完成签到,获得积分10
33秒前
ren发布了新的文献求助10
34秒前
azq完成签到,获得积分10
35秒前
香蕉梨愁完成签到,获得积分10
36秒前
高分求助中
Clinical Epidemiology: The Essentials, 6e 10000
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
The Graphene Handbook (2019 Edition) 800
Adhesion Science: Principles & Practice 800
Signals, Systems, and Signal Processing 610
Fundamentals of Pharmaceutical and Biologics Regulations: A Global Perspective, Second Edition 600
The Immune System (Fifth Edition) 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6568180
求助须知:如何正确求助?哪些是违规求助? 8347779
关于积分的说明 17885285
捐赠科研通 5695137
什么是DOI,文献DOI怎么找? 2944040
邀请新用户注册赠送积分活动 1919936
关于科研通互助平台的介绍 1795942