Poste G, Papahadjopoulos D
Proc Natl Acad Sci U S A. 1976 May;73(5):1603-7. doi: 10.1073/pnas.73.5.1603.
The mechanisms involved in the uptake of uni- and multi-lamellar lipid vesicles by BALB/c mouse 3T3 cells have been investigated. Vesicles are incorporated into cells both by endocytosis and by a nonendocytotic mechanism which we propose involves fusion of vesicles with the plasma membrane. The nonendocytotic pathway predominates in the uptake of negatively charged vesicles composed of phospholipids that are "fluid" (phosphatidylserine/phosphatidylcholine) at 37 degrees. Neutral fluid vesicles (phosphatidylcholine) and negatively charged vesicles prepared from "solid" phospholipids (phosphatidylserine/distearylphosphatidylcholine/dipalmitoylphosphatidylcholine) are instead incorporated largely by endocytosis. Uptake of the latter classes of vesicle is reduced (80-90% inhibition) by inhibitors of cellular energy metabolism and by cytochalasin B.
已对BALB/c小鼠3T3细胞摄取单层和多层脂质囊泡的机制进行了研究。囊泡通过内吞作用和一种非内吞机制进入细胞,我们认为这种非内吞机制涉及囊泡与质膜的融合。在37℃时,由“流动性”磷脂(磷脂酰丝氨酸/磷脂酰胆碱)组成的带负电荷囊泡的摄取中,非内吞途径占主导。相反,中性流动性囊泡(磷脂酰胆碱)和由“固态”磷脂(磷脂酰丝氨酸/二硬脂酰磷脂酰胆碱/二棕榈酰磷脂酰胆碱)制备的带负电荷囊泡主要通过内吞作用被摄取。细胞能量代谢抑制剂和细胞松弛素B可减少后一类囊泡的摄取(抑制80 - 90%)。