Prasmickaite L, Høgset A, Tjelle T E, Olsen V M, Berg K
Department of Biophysics, Institute for Cancer Research, The Norwegian Radium Hospital, Montebellow, Oslo.
J Gene Med. 2000 Nov-Dec;2(6):477-88. doi: 10.1002/1521-2254(200011/12)2:6<477::AID-JGM137>3.0.CO;2-B.
Most non-viral gene therapy vectors deliver transgenes into cells through the endocytic pathway. Lack of escape from endocytic vesicles in many cases constitutes a major barrier for delivery of the functional gene. We have developed a new technology named photochemical internalisation (PCI) to achieve light-inducible cytosolic delivery of the transgene. The technology is based on a photochemical treatment employing photosensitisers localised in endocytic vesicles. In this work mechanisms involved in PCI-mediated transfection (photochemical transfection) were studied.
Human melanoma or colon carcinoma cells were pre-incubated with the photosensitiser aluminium phthalocyanine disulfonate (AlPcS2a) followed by treatment with plasmid encoding enhanced green fluorescent protein (EGFP) complexed with poly-L-lysine, N-(1-(2,3-dioleoxyloxy)propyl)-N,N,N,-trimethylammonium-methyl-sulfate (DOTAP) or polyethylenimine (PEI) and light exposure. The expression of the EGFP-gene was scored by fluorescence microscopy and flow cytometry.
The photochemical treatment using light doses corresponding to D50 substantially improves the efficiency of transfection mediated by poly-L-lysine and PEI, but not by DOTAP. The treatment does not enhance the delivery of the plasmid complex across the plasma membrane, since the amount of internalised plasmid is similar for irradiated and non-irradiated cells. Light-inducible transfection occurs only under temperature conditions allowing endocytic uptake and is not improved by chloroquine or ammonium chloride, but is inhibited by bafilomycin A1 (agents that increase vesicular pH and interfere with the endocytic transport).
Photochemical transfection occurs through endocytosis, followed by cytosolic release of the transfecting DNA from photochemically permeabilised endocytic vesicles. Release of plasmid from early endosomes seems to be of importance in photochemical transfection, although a role of later endocytic vesicles can, however, not be ruled out.
大多数非病毒基因治疗载体通过内吞途径将转基因导入细胞。在许多情况下,无法从内吞小泡中逃逸是功能性基因递送的主要障碍。我们开发了一种名为光化学内化(PCI)的新技术,以实现转基因的光诱导胞质递送。该技术基于使用定位于内吞小泡的光敏剂的光化学处理。在这项工作中,研究了PCI介导的转染(光化学转染)所涉及的机制。
将人黑色素瘤或结肠癌细胞与光敏剂二磺酸铝酞菁(AlPcS2a)预孵育,然后用与聚-L-赖氨酸、N-(1-(2,3-二油酰氧基)丙基)-N,N,N-三甲基铵甲基硫酸盐(DOTAP)或聚乙烯亚胺(PEI)复合的编码增强型绿色荧光蛋白(EGFP)的质粒处理并进行光照。通过荧光显微镜和流式细胞术对EGFP基因的表达进行评分。
使用对应于D50的光剂量进行光化学处理可显著提高聚-L-赖氨酸和PEI介导的转染效率,但不能提高DOTAP介导的转染效率。该处理不会增强质粒复合物跨质膜的递送,因为照射和未照射细胞内化的质粒量相似。光诱导转染仅在允许内吞摄取的温度条件下发生,不受氯喹或氯化铵的影响,但被巴弗洛霉素A1(增加囊泡pH值并干扰内吞运输的试剂)抑制。
光化学转染通过内吞作用发生,随后转染DNA从光化学通透的内吞小泡中释放到胞质中。早期内体中质粒的释放似乎在光化学转染中起重要作用,尽管后期内吞小泡的作用也不能排除。