半胱氨酸蛋白酶 cathepsin B 可促进溶酶体的完整性,从而延长隔日禁食蠕虫的寿命。

IF 8 1区 医学 Q1 CELL BIOLOGY Aging Cell Pub Date : 2024-07-24 DOI:10.1111/acel.14286
Xue Yin, Fangzhou Dai, Dongyang Ran, Yutong Zhang, Zhi Qu, Shanqing Zheng
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引用次数: 0

摘要

研究表明,替代性一日禁食(ADF)能延长动物的寿命。然而,评估 ADF 疗效的人体试验最近才出现,由于这种饮食疗法的极端性质,带来了挑战。为了更好地了解 ADF 的效果,我们以 elegans(秀丽隐杆线虫)为模式生物研究了它的影响。我们的研究结果表明,ADF能延长以动物性蛋白质为主要蛋白质来源的蠕虫的寿命,而以植物性蛋白质为主要蛋白质来源的蠕虫则没有这种益处。值得注意的是,在中年期开始使用 ADF 足以延长寿命,而在青年期使用 ADF 则会导致发育受损,在老年期使用 ADF 则无法提供额外的延长寿命效果。此外,我们还发现,中年ADF能上调两种半胱氨酸蛋白酶cathepsin B基因(cpr-2和cpr-5)的表达,从而保持溶酶体的完整性,增强其消化聚集蛋白的功能,并促进脂质代谢,改善衰老过程中的神经退行性疾病标志物和现象。这表明,中年ADF具有持久的抗衰老作用,并可能延缓相关疾病的发生,特别是在食用动物蛋白质来源的动物中。这些发现为了解 ADF 的作用提供了宝贵的见解,并为今后的研究和在个人身上的潜在应用提供了指导。
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Cysteine protease cathepsin B promotes lysosome integrity to extend the lifespan of alternative day fasting worms.

Alternative day fasting (ADF) has been shown to enhance the lifespan of animals. However, human trials evaluating the efficacy of ADF have only recently emerged, presenting challenges due to the extreme nature of this dietary regimen. To better understand the effects of ADF, we investigated its impact using Caenorhabditis elegans as a model organism. Our findings reveal that ADF extends the lifespan of worms nourished on animal-based protein source, while those fed with plant-based protein as the primary protein source do not experience such benefits. Remarkably, initiating ADF during midlife is sufficient to prolong lifespan, whereas implementation during youth results in developmental damage, and in older age, fails to provide additional extension effects. Furthermore, we discovered that midlife ADF up-regulates the expression of two cysteine protease cathepsin B genes, cpr-2 and cpr-5, which preserve lysosomal integrity and enhance its function in digesting aggregated proteins, as well as enhancing lipid metabolism and ameliorating neurodegenerative disease markers and phenomena during aging. This suggests that midlife ADF has long lasting anti-aging effects and may delay the onset of related diseases, specifically in animals consuming animal-based protein source. These findings offer valuable insights into the effects of ADF and provide guidance for future research and potential applications in individuals.

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来源期刊
Aging Cell
Aging Cell Biochemistry, Genetics and Molecular Biology-Cell Biology
自引率
2.60%
发文量
212
期刊介绍: Aging Cell is an Open Access journal that focuses on the core aspects of the biology of aging, encompassing the entire spectrum of geroscience. The journal's content is dedicated to publishing research that uncovers the mechanisms behind the aging process and explores the connections between aging and various age-related diseases. This journal aims to provide a comprehensive understanding of the biological underpinnings of aging and its implications for human health. The journal is widely recognized and its content is abstracted and indexed by numerous databases and services, which facilitates its accessibility and impact in the scientific community. These include: Academic Search (EBSCO Publishing) Academic Search Alumni Edition (EBSCO Publishing) Academic Search Premier (EBSCO Publishing) Biological Science Database (ProQuest) CAS: Chemical Abstracts Service (ACS) Embase (Elsevier) InfoTrac (GALE Cengage) Ingenta Select ISI Alerting Services Journal Citation Reports/Science Edition (Clarivate Analytics) MEDLINE/PubMed (NLM) Natural Science Collection (ProQuest) PubMed Dietary Supplement Subset (NLM) Science Citation Index Expanded (Clarivate Analytics) SciTech Premium Collection (ProQuest) Web of Science (Clarivate Analytics) Being indexed in these databases ensures that the research published in Aging Cell is discoverable by researchers, clinicians, and other professionals interested in the field of aging and its associated health issues. This broad coverage helps to disseminate the journal's findings and contributes to the advancement of knowledge in geroscience.
期刊最新文献
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