mTORC1型
小干扰RNA
纳米载体
衰老
可药性
基因沉默
细胞生物学
PI3K/AKT/mTOR通路
DNA损伤
化学
DNA
生物
信号转导
药品
核糖核酸
药理学
生物化学
基因
作者
Ziqi Yue,Yichen Yang,Lulingxiao Nie,Yuezhang Sun,Qi Wang,Yunfeng Lin,Yang Gao,Xiaoxiao Cai
出处
期刊:Small
[Wiley]
日期:2024-12-17
卷期号:21 (18): e2408323-e2408323
标识
DOI:10.1002/smll.202408323
摘要
Abstract Extensive accumulation of senescent cells contributes to organismal aging, and slowing down the process of cellular senescence may ameliorate age‐related pathologies. Targeted inhibition of the mechanistic target of rapamycin complex 1 (mTORC1) is found to suppress the conversion of cells to senescence. The regulatory‐associated protein of mTOR (Raptor), a key component of mTORC1, has been implicated as important in the aging process, and its druggability deserves to be investigated. Due to high efficiency and high convenience in drug construction, siRNA shows great potential in silencing Raptor expression via RNA interfering therapy. Here, we developed a functionalized anti‐aging nanoplatform based on tetrahedral DNA nanostructures (TDNs) encapsulating siRNA targeting Raptor for synergistic anti‐aging therapy, named siR‐TDN box . Anti‐inflammatory and antioxidant properties of TDN beneficially attenuate age‐associated inflammation while serving as siRNA nanocarrier, and thus play a binary role. The results suggest that the siR‐TDN box binary therapeutic nanoplatform has demonstrated an excellent ability to delay aging, inhibit mTORC1 signaling, and extend lifespan. This anti‐aging nanoplatform may provide a medium for the combined application of traditional senotherapeutic drugs and promote the upgrading of nanomaterials with anti‐aging effects.
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