Department of Medical Bioengineering, Okayama University, Okayama, Japan.
Department of Interdisciplinary Science and Engineering in Health Systems, Okayama University, Okayama, Japan.
Photochem Photobiol. 2019 Nov;95(6):1395-1402. doi: 10.1111/php.13146. Epub 2019 Aug 24.
The inefficient endosomal escape of drugs or macromolecules is a major obstacle to achieving successful delivery to therapeutic targets. An efficient approach to circumvent this barrier is photochemical internalization (PCI), which uses light and photosensitizers for endosomal escape of the delivered macromolecules. The PCI mechanism is related to photogenerated singlet oxygen, but the mechanism is still unclear. In this study, we examined the relation of PCI to heat, pH and Ca ions using cell penetrating peptide (CPP)-cargo-photosensitizer (Alexa546 or Alexa633) conjugates. A cell temperature changing experiment demonstrated that heat (thermal mechanism) does not significantly contribute to the photoinduced endosomal escape. Inhibition of V-ATPase proton pump activity and endosomal pH upregulation indicated that PCI-mediated endosomal escape needs endosomal acidification prior to photoirradiation. Imaging of the CPP-cargo-photosensitizer and Ca ions during photostimulation showed that intracellular calcium increase is not the cause of the endosomal escape of the complex. The increment is mainly due to Ca influx. These findings show the importance of extra- and intracellular milieu conditions in the PCI mechanism and enrich our understanding of PCI-related changes in cell.
药物或大分子的内体逃逸效率低下是实现治疗靶点有效递送的主要障碍。规避这一障碍的一种有效方法是光化学内化(PCI),它利用光和光敏剂实现递送至细胞内的大分子的内体逃逸。PCI 机制与光生成的单线态氧有关,但机制尚不清楚。在这项研究中,我们使用穿透肽(CPP)-货物-光敏剂(Alexa546 或 Alexa633)缀合物研究了 PCI 与热、pH 和 Ca 离子的关系。细胞温度变化实验表明,热(热机制)对光诱导的内体逃逸没有显著贡献。抑制 V-ATPase 质子泵活性和内体 pH 上调表明,PCI 介导的内体逃逸需要在光照射前进行内体酸化。在光刺激过程中对 CPP-货物-光敏剂和 Ca 离子进行成像显示,细胞内钙离子的增加不是复合物内体逃逸的原因。这种增加主要是由于 Ca 内流。这些发现表明细胞内、外环境条件在 PCI 机制中的重要性,并丰富了我们对 PCI 相关细胞变化的理解。