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苄青霉素在小鼠腹膜巨噬细胞单层中的转运及亚细胞分布

Benzylpenicillin transport and subcellular distribution in mouse peritoneal macrophage monolayers.

作者信息

Lowrie D B, Peters T J, Scoging A

出版信息

Biochem Pharmacol. 1982 Feb 1;31(3):423-32. doi: 10.1016/0006-2952(82)90193-9.

Abstract

[14C]Benzylpenicillin was rapidly taken up into and eluted from mouse peritoneal macrophage monolayers and entered cytosol, lysosomes and phagolysosomes containing Staphylococcus aureus. Equilibrium concentrations in cytosol and lysosomes were consistent with transport by diffusion but partial membrane carrier dependence was evidenced by saturability (Km and Vmax 110 mM and 117 nmoles (10(6) cells)-1 (3 min)-1 respectively) and inhibition by probenecid. Partial dependence of transport on metabolic energy was shown by inhibition with cyanide plus 2-deoxyglucose and the temperature coefficient (Q10) was about 2. Some of the intralysosomal radiolabel accumulated as benzylpenicilloic acid.

摘要

[14C]苄青霉素能迅速被小鼠腹腔巨噬细胞单层摄取并洗脱,进入含有金黄色葡萄球菌的胞质溶胶、溶酶体和吞噬溶酶体。胞质溶胶和溶酶体中的平衡浓度与通过扩散的转运一致,但饱和性(Km和Vmax分别为110 mM和117纳摩尔(10⁶个细胞)⁻¹(3分钟)⁻¹)和丙磺舒的抑制作用证明了对部分膜载体的依赖性。用氰化物加2-脱氧葡萄糖抑制表明转运对代谢能量有部分依赖性,温度系数(Q10)约为2。一些溶酶体内的放射性标记物以苄青霉素酸的形式积累。

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