Gwak HyeRan, Hong Seoyoung, Lee Su Hyun, Kim In Woo, Kim Yonghan, Kim Hyungmin, Pahk Ki Joo, Kim So Yeon
Chemical and Biological Integrative Research Center, Biomedical Research Division, Korea Institute of Science and Technology, Seoul, Republic of Korea.
Bionics Research Center, Biomedical Research Division, Korea Institute of Science and Technology, Seoul, Republic of Korea.
Aging Cell. 2025 May;24(5):e14486. doi: 10.1111/acel.14486. Epub 2025 Jan 16.
As emerging therapeutic strategies for aging and age-associated diseases, various biochemical approaches have been developed to selectively remove senescent cells, but how physical stimulus influences senescent cells and its possible application in senolytic therapy has not been reported yet. Here we developed a physical method to selectively stimulate senescent cells via low-intensity pulsed ultrasound (LIPUS) treatment. LIPUS stimulation did not affect the cell cycle, but selectively enhanced secretion of specific cytokines in senescent cells, known as the senescence-associated secretory phenotype (SASP), resulting in enhanced migration of monocytes/macrophages and upregulation of phagocytosis of senescent cells by M1 macrophage. We found that LIPUS stimulation selectively perturbed the cellular membrane structure in senescent cells, which led to activation of the intracellular reactive oxygen species-dependent p38-NF-κB signaling pathway. Using a UV-induced skin aging mouse model, we confirmed enhanced macrophage infiltration followed by reduced senescent cells after LIPUS treatment. Due to the advantages of ultrasound treatment, such as non-invasiveness, deep penetration capability, and easy application in clinical settings, we expect that our method can be applied to treat various senescence-associated diseases or combined with other established biochemical therapies to enhance efficacy.
作为针对衰老及与年龄相关疾病的新兴治疗策略,人们已开发出各种生化方法来选择性清除衰老细胞,但物理刺激如何影响衰老细胞及其在衰老细胞溶解疗法中的潜在应用尚未见报道。在此,我们开发了一种物理方法,通过低强度脉冲超声(LIPUS)治疗选择性刺激衰老细胞。LIPUS刺激不影响细胞周期,但能选择性增强衰老细胞中特定细胞因子的分泌,即所谓的衰老相关分泌表型(SASP),从而导致单核细胞/巨噬细胞迁移增强以及M1巨噬细胞对衰老细胞吞噬作用上调。我们发现,LIPUS刺激选择性扰乱了衰老细胞的细胞膜结构,进而激活了细胞内依赖活性氧的p38-NF-κB信号通路。利用紫外线诱导的皮肤衰老小鼠模型,我们证实LIPUS治疗后巨噬细胞浸润增强,随后衰老细胞减少。鉴于超声治疗具有非侵入性、深层穿透能力以及在临床环境中易于应用等优点,我们期望我们的方法能够应用于治疗各种与衰老相关的疾病,或与其他已确立的生化疗法联合使用以提高疗效。