4.8 Article

VB12-Sericin-PBLG-IR780 Nanomicelles for Programming Cell Pyroptosis via Photothermal (PTT)/Photodynamic (PDT) Effect-Induced Mitochondrial DNA (mitoDNA) Oxidative Damage

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 14, 期 15, 页码 17008-17021

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c22804

关键词

photothermal/photodynamic therapy; mitochondrial DNA; oxidative damage; pyroptosis; nanomicelles

资金

  1. Guangdong Provincial Key Laboratory of Precision Medicine for Gastrointestinal Cancer [2020B121201004]
  2. Guangdong Provincial Major Talents Project [2019JC05Y361]
  3. National Natural Science Foundation of China [82001948, 81971746]
  4. Medical Scientific Research Foundation of Guangdong Province of China [A2020297]
  5. Special Funds for Cultivation of Guangdong College Students' Scientific and Technological Innovation [pdjh2021b0099]
  6. College Students' Innovative Entrepreneur ial Training Plan Program [202112121005, 202112121200, S202112121101, S202012121051]

向作者/读者索取更多资源

In this study, VB12-sericin-PBLG-IR780 nanomicelles were successfully synthesized, which can induce pyroptosis through photothermal effect and promote DC maturation and activate antitumor immunity.
Pyroptosis, a kind of programmed cell death involving inflammation, might be a powerful way to fight against tumors, for example, using immunotherapy. However, how to trigger pyroptosis in cancer cells is an important issue. Photothermal (PTT)/photodynamic (PDT) therapy is a crucial strategy for inducing cancer cell pyroptosis with noninvasiveness. In this work, a sericin derivative modified with poly(gamma-benzyl-L-glutamate) (PBLG) could self-assemble and was stable in an aqueous environment. Furthermore, the sericin derivative was conjugated with the tumor-targeting agent VB12 and loaded with IR780. Finally, we successfully synthesized VB12-sericin-PBLG-IR780 nanomicelles. The as-designed nanomicelles showed appropriate particle sizes, spherical morphology, improved photothermal stability, and high photothermal conversion efficiency (similar to 40%), which generated reactive oxygen species (ROS) simultaneously. Through enhanced cellular uptake, VB12-sericin-PBLG-IR780 could deliver more IR780 into cancer cells. With near-infrared (NIR), the VB12-sericin-PBLG-IR780 could significantly inhibit the expression of ATP synthase, called ATP5MC3, followed by mitochondrial damage. The presence of mitochondrial reactive oxygen species (mitoROS) led to oxidative damage of mitochondrial DNA (mitoDNA), which further activates NLRP3/Caspase-1/gasdermin D (GSDMD)-dependent pyroptosis and could promote dendritic cell (DC) maturation by pyroptosis. Furthermore, our data showed that VB12-sericin-PBLG-IR780 could achieve a brilliant antitumor effect and could activate DC maturation, initiate T-cell recruiting, and prime adaptive antitumor efficiency. Overall, our well-prepared nanomicelles might offer a tumor-targeted approach for programmed cell pyroptosis and inducing antitumor immunity via photothermal PTT/PDT effect-induced mitoDNA oxidative damage.

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