The anti-aging mechanisms of Catalpol by elevating mitophagy

生物 粒体自噬 梓醇 细胞生物学 线粒体 酵母 功能(生物学) 机制(生物学) 品脱1 程序性细胞死亡 计算生物学 细胞 模式生物 细胞内 生物化学 突变 遗传学 焊剂(冶金) 表型 自噬
作者
Songtao Bie,Ze Kun Yao,Ming Lu,Chunshuang Li,Xiang Li,Shanghui Lu
出处
期刊:Gene [Elsevier BV]
卷期号:969: 149765-149765 被引量:1
标识
DOI:10.1016/j.gene.2025.149765
摘要

• Enhancement of Cell Viability : Treatment with Catalpol (CAT) significantly increases the viability of yeast cells, suggesting its potential role as an anti-aging agent by promoting cell health and function. • Identification of HSP82 as a Key Target : RNA-Seq and bioinformatics analyses identified HSP82 as a critical target of CAT, linking it to the regulation of mitophagy and mitochondrial activity in the context of aging. • HSP82 -Dependent Mitophagy : The study demonstrated that CAT enhances mitochondrial functions and extends the lifespan of yeast cells via HSP82 -dependent mitophagy, highlighting its importance in cellular maintenance. • Mechanistic Insights into Anti-Aging Effects : The research reveals the molecular mechanisms through which CAT exerts anti-aging effects, particularly by modulating mitophagy pathways to improve cell longevity. • Potential for Treating Age-Related Diseases : Findings indicate that CAT could serve as a promising therapeutic candidate for addressing age-related diseases by enhancing mitophagy and promoting mitochondrial health. Autophagy is an important mechanism for maintaining cell homeostasis, and its decline in function is widely regarded as a key factor in aging. Catalpol (CAT), an active compound derived from the traditional Chinese herb Rehmannia glutinosa , has shown potential to treat various age-related diseases through the regulation of autophagy. However, how CAT exerts anti-aging effects by regulating autophagy remains unclear. Therefore, this study sought to explore the anti-aging potential and molecular mechanisms, particularly the role of CAT in autophagy and mitochondrial function in yeast cells. The PI-CLS measurement method was employed to demonstrate enhanced yeast cells viability upon CAT treatment. RNA-Seq combined with bioinformatics analyses identified HSP82 as a key target of CAT. HSP82 knockout and HSP82 overexpression strains were employed to demonstrate that CAT enhances mitochondrial functions and extends cells lifespan by inducing HSP82 -dependent mitophagy. We concluded that CAT plays an anti-aging role by regulating HSP82 -dependent mitophagy and mitochondrial functions in yeast cells.
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