4.7 Article

Apoptosis of THP-1 macrophages induced by protoporphyrin IX-mediated sonodynamic therapy

期刊

INTERNATIONAL JOURNAL OF NANOMEDICINE
卷 8, 期 -, 页码 2239-2246

出版社

DOVE MEDICAL PRESS LTD
DOI: 10.2147/IJN.S43717

关键词

sonodynamic therapy; protoporphyrin IX; atherosclerotic plaque; macrophage; singlet oxygen; cytoskeleton

资金

  1. National Natural Science Foundation of China [30970786, 81101164, 81171483]
  2. Scientific and Technical Key Task of Heilongjiang Province, People's Republic of China [GC10C306]
  3. Funds for Creative Research Groups of the National Natural Science Foundation of China [81121003]

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Background: Sonodynamic therapy (SDT) was developed as a localized ultrasound-activated cytotoxic therapy for cancer. The ability of SDT to destroy target tissues selectively is especially appealing for atherosclerotic plaque, in which selective accumulation of the sonosensitizer, protoporphyrin IX (PpIX), had been demonstrated. Here we investigate the effects of PpIX-mediated SDT on macrophages, which are the main culprit in progression of atherosclerosis. Methods and results: Cultured THP-1 derived macrophages were incubated with PpIX. Fluorescence microscopy showed that the intracellular PpIX concentration increased with the concentration of PpIX in the incubation medium. MTT assay demonstrated that SDT with PpIX significantly decreased cell viability, and this effect increased with duration of ultrasound exposure and PpIX concentration. PpIX-mediated SDT induced both apoptosis and necrosis, and the maximum apoptosis to necrosis ratio was obtained after SDT with 20 mu g/mL PpIX and five minutes of sonication. Production of intracellular singlet oxygen and secondary disruption of the cytoskeleton were also observed after SDT with PpIX. Conclusion: PpIX-mediated SDT had apoptotic effects on THP-1 macrophages via generation of intracellular singlet oxygen and disruption of the cytoskeleton. PpIX-mediated SDT may be a potential treatment to attenuate progression of atherosclerotic plaque.

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