Yu Wenzhuo, Jia Xu, Qiao Han, Liu Di, Sun Yan, Yan Rong, Zhang Chenglong, Yu Na, Song Yiping, Ling Mingying, Zhang Zhen, Li Xuehui, Zhao Chuanli, Xing Yanqiu
Department of Geriatric Medicine, Qilu Hospital of Shandong University, 250012 Jinan, Shandong, China.
Division of Bacterial Anti-tumor Drugs, Shandong Precision Medicine Engineering Laboratory, Shandong Xinchuang Biotechnology Co., LTD, Jinan, Shandong, China.
J Proteomics. 2025 Jan 6;310:105335. doi: 10.1016/j.jprot.2024.105335. Epub 2024 Oct 20.
Aging is a critical biological process, with particularly notable impacts on the kidneys. Exosomes derived from human umbilical cord mesenchymal stem cells (hUC-MSCs) are capable of transferring various bioactive molecules, which exhibit beneficial therapeutic effects on kidney diseases. This study demonstrates that exosomes derived from hUC-MSCs ameliorate cellular senescence in the kidneys of naturally aging mice. These exosomes reduce the protein expression of senescence markers and senescence-associated secretory phenotypes (SASP) leading to fewer DNA damage foci and increased expression of the proliferation indicator Ki67. During the aging process, many proteins undergo phosphorylation modifications. We utilized data-independent acquisition (DIA) phosphoproteomics to study kidneys of naturally aging mice and those treated with hUC-MSC-derived exosomes. We observed elevated phosphorylation levels of the differentially phosphorylated proteins, Lamin A/C, at Ser390 and Ser392 sites, which were subsequently verified by western blotting. Overall, this study provides a new molecular characterization of hUC-MSC-derived exosomes in mitigating cellular senescence in the kidneys. SIGNIFICANCE: DIA phosphoproteomics was employed to investigate phosphorylated proteins in the kidney tissues of naturally aging mice with hUCMSC-exos treated. The results demonstrated that the DIA technique detected a higher abundance of phosphorylated proteins. We identified 24 significantly differentially phosphorylated proteins, and found that the phosphorylation of specific Lamin A/C sites is crucial for preventing cellular senescence. This study will help to better reveal the related phosphorylated proteins involved in hUCMSC-exos intervention in the kidneys of naturally aging mice, providing a foundation for future research on specific phosphorylation sites of proteins as potential therapeutic targets for renal aging-related diseases.
衰老 是一个关键的生物学过程,对肾脏的影响尤为显著。源自人脐带间充质干细胞(hUC-MSCs)的外泌体能够传递各种生物活性分子,对肾脏疾病具有有益的治疗作用。本研究表明,源自hUC-MSCs的外泌体可改善自然衰老小鼠肾脏中的细胞衰老。这些外泌体降低了衰老标志物和衰老相关分泌表型(SASP)的蛋白表达,从而减少DNA损伤灶,并增加增殖指标Ki67的表达。在衰老过程中,许多蛋白质会发生磷酸化修饰。我们利用数据非依赖采集(DIA)磷酸化蛋白质组学研究自然衰老小鼠以及用hUC-MSC来源的外泌体处理的小鼠的肾脏。我们观察到差异磷酸化蛋白核纤层蛋白A/C在Ser390和Ser392位点的磷酸化水平升高,随后通过蛋白质印迹法进行了验证。总体而言,本研究为hUC-MSC来源的外泌体减轻肾脏细胞衰老提供了新的分子特征。意义:采用DIA磷酸化蛋白质组学研究经hUCMSC-外泌体处理的自然衰老小鼠肾脏组织中的磷酸化蛋白质。结果表明,DIA技术检测到更高丰度的磷酸化蛋白质。我们鉴定出24种显著差异磷酸化的蛋白质,并发现特定核纤层蛋白A/C位点的磷酸化对于预防细胞衰老至关重要。本研究将有助于更好地揭示参与hUCMSC-外泌体干预自然衰老小鼠肾脏的相关磷酸化蛋白质,为未来将蛋白质的特定磷酸化位点作为肾脏衰老相关疾病潜在治疗靶点的研究奠定基础。