Wilson T, Papahadjopoulos D, Taber R
Cell. 1979 May;17(1):77-84. doi: 10.1016/0092-8674(79)90296-4.
Large unilamellar vesicles (LUV) composed of phosphatidylserine are capable of encapsulating poliovirus ribonucleic acid (RNA) and delivering it efficiently to cells in an infectious form. The biological activity of vesicle-entrapped poliovirus RNA was 1-2 x 10(4) plaque forming units/nanogram (pfu/ng) and appeared to be enhanced by ribonuclease treatment of the vesicle preparations (infectivity = 1-2 x 10(5) pfu/ng). Vesicle-mediated RNA infection produced equivalent titers in primate and nonprimate cells. Moreover, the data strongly suggest that the ratio of molecules per infectious unit is close to one when the RNA is properly delivered to the cell. A comparative study of LUV and multilamellar vesicles (MLV) indicates that LUV deliver their contents to the cell cytoplasm much more efficiently than MLV. LUV-entrapped poliovirus RNA produced infectious titer 10-100 fold higher than comparable RNA preparations delivered to cells by other techniques.
由磷脂酰丝氨酸组成的大单层囊泡(LUV)能够包裹脊髓灰质炎病毒核糖核酸(RNA),并以感染性形式将其高效递送至细胞。囊泡包裹的脊髓灰质炎病毒RNA的生物活性为1 - 2×10⁴ 蚀斑形成单位/纳克(pfu/ng),并且通过对囊泡制剂进行核糖核酸酶处理,其活性似乎有所增强(感染性 = 1 - 2×10⁵ pfu/ng)。囊泡介导的RNA感染在灵长类和非灵长类细胞中产生的滴度相当。此外,数据有力地表明,当RNA被正确递送至细胞时,每个感染单位的分子比例接近1。对LUV和多层囊泡(MLV)的比较研究表明,LUV将其内容物递送至细胞质的效率比MLV高得多。LUV包裹的脊髓灰质炎病毒RNA产生的感染滴度比通过其他技术递送至细胞的可比RNA制剂高10 - 100倍。