MECHANISM OF POLYCATION STIMULATION OF PINOCYTOSIS

被引:35
作者
DUNCAN, R
PRATTEN, MK
LLOYD, JB
机构
[1] Biochemistry Research Laboratory, Department of Biological Sciences, University of Keele, Keele
关键词
(Peritoneal macrophage; Yolk sac); Endocytic index; Pinocytosis; Polycation stimulation;
D O I
10.1016/0304-4165(79)90450-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Synthetic polycations cause a stimulation in the rate of tissue accumulation of colloidal 198Au by the rat visceral yolk sac (at 17.5 days of gestaton) and rat peritoneal macrophages cultured in vitro. The mechanism of stimulation has been elucidated in these two cell types by using a dual-substrate technique, and by examining the differential effects of poly(d-lysine) and poly(l-lysine) and of metabolic and cytoskeletal inhibitors. Polycations cause aggregation of colloidal 198Au in the culture medium and increase its affinity for the plasma membrane. In the rat peritoneal macrophage this polycation-colloidal gold complex is pinocytosed, thus enhancing the intracellular accumulation of the radiolabelled substrate. In contrast, the rat viscerak yolk sac cannot internalize this complex, and so the substrate accumulates extracellularly. This mechanism of polycation modification affords the opportunity for differential uptake of a substrate into distinct cell types. © 1979.
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页码:463 / 475
页数:13
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