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大鼠肾上腺中线粒体内胆固醇向侧链裂解细胞色素P-450的转运调节

Regulation of intramitochondrial cholesterol transfer to side-chain cleavage cytochrome P-450 in rat adrenal gland.

作者信息

Privalle C T, Crivello J F, Jefcoate C R

出版信息

Proc Natl Acad Sci U S A. 1983 Feb;80(3):702-6. doi: 10.1073/pnas.80.3.702.

Abstract

Rat adrenal mitochondria accumulated cholesterol during ether stress in vivo when side-chain cleavage was inhibited by aminoglutethimide (control = 14.6 vs. aminoglutethimide = 26.5 micrograms of cholesterol per mg of protein). This accumulation was insensitive to simultaneous administration of cycloheximide (24.2 micrograms/mg), but side chain cleavage in the mitochondria was greatly decreased. Outer and inner mitochondrial membrane fractions were separated by discontinuous Ficoll gradient centrifugation. Quantitation of marker enzymes for inner, outer, and microsomal enzymes indicated that outer membranes contained less than 5% inner membranes. The inner membrane fraction contained less than 7% outer membrane and included 90% of mitochondrial cytochrome P-450. Electron microscopy revealed outer membranes as circular intact ghosts, whereas inner membranes were largely intact and retained vesicular structure typical of intact adrenal cortex mitochondria. Administration of aminoglutethimide effected a 2-fold increase in inner membrane cholesterol (9.4 vs. 20.1 micrograms/mg) but simultaneous administration of cycloheximide completely blocked this increase (10.9 micrograms/mg). We conclude that: (i) in the presence of aminoglutethimide, stress stimulates accumulation of cholesterol in the inner membrane of adrenal mitochondria; and (ii) transfer of cholesterol from outer to inner membranes requires a cycloheximide-sensitive agent.

摘要

当氨基导眠能抑制侧链裂解时,大鼠肾上腺线粒体在体内乙醚应激期间会积累胆固醇(对照组 = 每毫克蛋白质含14.6微克胆固醇,氨基导眠能组 = 每毫克蛋白质含26.5微克胆固醇)。这种积累对同时给予环己酰亚胺不敏感(24.2微克/毫克),但线粒体中的侧链裂解大大减少。通过不连续的Ficoll梯度离心分离线粒体外膜和内膜部分。对内膜、外膜和微粒体酶的标记酶进行定量分析表明,外膜中内膜含量不到5%。内膜部分中外膜含量不到7%,且包含90%的线粒体细胞色素P-450。电子显微镜显示外膜为完整的圆形空壳,而内膜基本完整并保留了完整肾上腺皮质线粒体典型的囊泡结构。给予氨基导眠能使内膜胆固醇增加了2倍(9.4微克/毫克对20.1微克/毫克),但同时给予环己酰亚胺则完全阻断了这种增加(10.9微克/毫克)。我们得出以下结论:(i)在存在氨基导眠能的情况下,应激会刺激肾上腺线粒体内膜中胆固醇的积累;(ii)胆固醇从外膜向内膜的转移需要一种对环己酰亚胺敏感的因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/859b/393447/c20d8b6ed91e/pnas00629-0058-a.jpg

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