Wattiaux R, Jadot M, Dubois F, Misquith S, Wattiaux-De Coninck S
Laboratoire de Chimie Physiologique, Facultés Universitaires Notre-Dame de la Paix, Namur, Belgium.
Biochem Biophys Res Commun. 1995 Aug 4;213(1):81-7. doi: 10.1006/bbrc.1995.2101.
We have investigated by using centrifugation methods, the uptake and the intracellular fate of 35S DNA by rat liver and the effect on these processes of N-(1-(2,3-dioleoxyloxy)propyl)-N,N,N,-trimethylammonium-methyl-sul fate(DOTAP, Boehringer, Mannheim, Germany), an artificial cationic lipid frequently used in transfection experiments. Labeled DNA molecules are quickly taken up by the liver but a progressive degradation takes place with time. Subcellular distribution of the radioactivity was established after differential and isopycnic centrifugation. Results indicate that 35S DNA enters liver cells by endocytosis and reaches lysosomes. The uptake of 35S DNA is not modified if the molecule is associated with DOTAP but marked differences are observed after internalization of the macromolecule. When DOTAP is used, radioactive products remain for a long time in low density organelles distinct from lysosomes indicating that the transfer of internalized DNA to these organelles is delayed by the cationic lipid. These results suggest that cationic lipids could favor transfection by preventing the delivery of DNA to lysosomes, allowing these molecules to be kept intact and available for transfer from endosomes to cytosol for a long time.
我们运用离心方法研究了大鼠肝脏对35S DNA的摄取及细胞内命运,以及N-(1-(2,3-二油酰氧基)丙基)-N,N,N-三甲基铵甲基硫酸盐(DOTAP,德国曼海姆勃林格公司生产)对这些过程的影响,DOTAP是转染实验中常用的一种人工合成阳离子脂质。标记的DNA分子迅速被肝脏摄取,但随着时间推移会逐渐降解。通过差速离心和等密度离心确定了放射性的亚细胞分布。结果表明,35S DNA通过内吞作用进入肝细胞并到达溶酶体。如果DNA分子与DOTAP结合,其摄取情况不会改变,但在大分子内化后会观察到明显差异。使用DOTAP时,放射性产物会在与溶酶体不同的低密度细胞器中长时间留存,这表明阳离子脂质会延迟内化DNA向这些细胞器的转运。这些结果表明,阳离子脂质可能通过阻止DNA进入溶酶体来促进转染,使这些分子保持完整并长时间可用于从内体转运至细胞质。