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用于声动力免疫治疗的可生物降解且具有压电性的锰掺杂羟基磷灰石

Biodegradable and Piezoelectric Mn-Doped Hydroxyapatite for Sonodynamic Immunotherapy.

作者信息

Cai Lihan, Han Fuping, Ding Junying, Zhou Xiao, Shi Tiancong, Cheng Fang, Peng Chong, Long Saran, Sun Wen, Fan Jiangli, Du Jianjun, Peng Xiaojun

机构信息

State Key Laboratory of Fine Chemicals, Frontiers Science Center for Smart Materials, Dalian University of Technology, Dalian, Liaoning 116024, P. R. China.

Ningbo Institute of Dalian University of Technology, 26 Yucai Road, Jiangbei District, Ningbo, Zhejiang 315016, P. R. China.

出版信息

ACS Nano. 2025 Jul 8;19(26):24067-24077. doi: 10.1021/acsnano.5c06775. Epub 2025 Jun 24.

DOI:10.1021/acsnano.5c06775
PMID:40554728
Abstract

The tumor microenvironment usually exhibits immunosuppressive characteristics, and pyroptosis is an effective method to stimulate antitumor immune responses. However, the current metal-ion-overload strategy to induce pyroptosis is hindered by the ion buffering system within the cell, which inhibits the release of exogenous ions. Herein, a biodegradable manganese-doped hydroxyapatite (Mn-HAP) with ultrasound (US) triggered continuous reactive oxygen species (ROS) modulation is proposed. Mn-HAP is defined as a sonoimmune stimulator because it functions as both a sonosensitizer and an immune agent. Before degradation, Mn-HAP exhibits an enhanced sonodynamic antitumor effect through the Mn-doping oxygen vacancies. Moreover, the built-in electric field induced by US activates the cell membrane-related ion channels and induces Ca influx. Following the degradation of Mn-HAP in the slightly acidic tumor microenvironment, the released Ca and ROS produced in sonodynamic therapy promote pyroptosis, while Mn activates the cGAS-STING pathway, triggering innate immunity and further enhancing the effect of pyroptosis-induced immunotherapy. This work provides a promising strategy for engineering biodegradable materials for the sonodynamic immunotherapy of solid tumors.

摘要

肿瘤微环境通常具有免疫抑制特性,而细胞焦亡是刺激抗肿瘤免疫反应的有效方法。然而,目前通过金属离子过载诱导细胞焦亡的策略受到细胞内离子缓冲系统的阻碍,该系统会抑制外源离子的释放。在此,我们提出了一种具有超声(US)触发的连续活性氧(ROS)调节功能的可生物降解的锰掺杂羟基磷灰石(Mn-HAP)。Mn-HAP被定义为一种声免疫刺激剂,因为它兼具声敏剂和免疫剂的功能。在降解之前,Mn-HAP通过锰掺杂的氧空位表现出增强的声动力抗肿瘤作用。此外,超声诱导的内建电场激活细胞膜相关离子通道并诱导钙离子内流。在微酸性肿瘤微环境中Mn-HAP降解后,释放的钙离子和在声动力疗法中产生的ROS促进细胞焦亡,而锰激活cGAS-STING途径,触发先天免疫并进一步增强细胞焦亡诱导的免疫治疗效果。这项工作为设计用于实体瘤声动力免疫治疗的可生物降解材料提供了一种有前景的策略。

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