...
首页> 外文期刊>Biochimica et biophysica acta. Biomembranes >Endocytosis and intracellular processing accompanying transfection mediated by cationic liposomes
【24h】

Endocytosis and intracellular processing accompanying transfection mediated by cationic liposomes

机译:阳离子脂质体介导的内吞和伴随转染的细胞内加工

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Cationic liposomes mediate efficient transfection of mammalian cells, but the manner in which cells internalize and process cationic liposome-DNA complexes has not been well characterized. We exposed several cell types, including human and murine erythroleukemia cells, African green monkey kidney cells (CV-1), isolated rat alveolar type II cells and alveolar macrophages to DNA-cationic liposome complexes containing N-(1-2,3-dioleyloxypropyl)-N,N,N-triethylammonium (DOTMA) and Dioleylphosphatidylethanolamine (DOPE). The morphology of liposome-cell interactions was assessed by electron microscopy. Liposome preparations were complexed to colloidal gold particles or to both plasmid DNA and gold particles. Cells treated with DOTMA liposome-DNA complexes demonstrated endocytosis of the liposome-DNA complexes in coated pits, which were seen in early endosomes, late endosomes, and lysosomes. In isolated alveolar type II cells, the gold-labelled DOTMA lipid apparently mixed with the contents of lamellar bodies. In most cells, gold particles were dispersed throughout the cytoplasmic matrix. In a small proportion of CV-1 and U937 cells, a membrane system resembling the endoplasmic reticulum developed within the nucleus. This novel structure was also present in nuclei after they were isolated from CV-1 cells and then mixed with DOTMA-containing liposomes. Membranes which form after exposure to DOTMA-containing liposomes were 10 nm in thickness as compared to the approx. 8 nm thickness of endogenous cellular membranes. Based on these morphologic observations, we propose that the main route of entry of cationic liposomes into cells is by endocytosis. In some instances, the endosomal compartment releases its cationic liposome-DNA contents into the cytoplasmic matrix. Occasionally, liposomes may enter the nucleus by fusion with the nuclear envelope, creating vesicular and reticular intranuclear membranes. It is not clear at present which, if any of these morphological observations correlates with transfection mediated by cationic liposomes.
机译:阳离子脂质体介导了哺乳动物细胞的有效转染,但是细胞内化和处理阳离子脂质体-DNA复合物的方式尚未得到很好的表征。我们将几种细胞类型暴露于含有N-(1-2,3-二醇基氧丙基)的DNA阳离子脂质体复合物中,包括人类和鼠类红白血病细胞,非洲绿猴肾细胞(CV-1),分离的大鼠II型肺泡细胞和肺泡巨噬细胞。 )-N,N,N-三乙铵(DOTMA)和二油基磷脂酰乙醇胺(DOPE)。通过电子显微镜评估脂质体-细胞相互作用的形态。将脂质体制剂与胶体金颗粒或质粒DNA和金颗粒复合。用DOTMA脂质体-DNA复合物处理的细胞在包被的凹坑中显示出脂质体-DNA复合物的内吞作用,这在早期的内体,晚期的内体和溶酶体中可见。在分离的II型肺泡细胞中,金标记的DOTMA脂质显然与片状体的内容物混合。在大多数细胞中,金颗粒分散在整个细胞质基质中。在一小部分CV-1和U937细胞中,类似于内质网的膜系统在细胞核内发育。从CV-1细胞中分离出来然后与含DOTMA的脂质体混合后,这种新结构也存在于细胞核中。暴露于含DOTMA的脂质体后形成的膜的厚度约为10 nm。内源性细胞膜的厚度为8 nm。基于这些形态学观察,我们提出阳离子脂质体进入细胞的主要途径是通过内吞作用。在某些情况下,内体区室将其阳离子脂质体-DNA含量释放到细胞质基质中。有时,脂质体可能会通过与核被膜融合而进入核内,形成囊泡和网状核内膜。目前尚不清楚,如果这些形态学观察中的任何一个与阳离子脂质体介导的转染有关。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号