静脉注射67cu标记的Cu-PTSM后组织放射性铜的亚细胞分布

Ingrid D. Baerga , Roger P. Maickel , Mark A. Green
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引用次数: 27

摘要

用铜-67标记的丙酮醛双(n4 -甲基硫代氨基脲)铜(II)静脉注射Cu-PTSM后,测定了放射性铜在大鼠大脑和肝脏中的亚细胞分布。匀浆后的组织样品经差速离心分离成四个亚细胞部分:(1)细胞膜+细胞核;(2)线粒体;(3)微粒体;(IV)细胞质。在牺牲在10分钟post-Cu-PTSM注入,大脑分数,I, II, III和IV包含35±12日11±3,2.8±1.3和51±7%的大脑活动,分别为(n = 4)。在动物牺牲24 h post-injection脑组织显示变化不大的亚细胞分数radiocopper分布在10分钟post-injection,尽管线粒体分数可能包含稍微示踪和胞质分数略低(我40±10%;Ii, 18±5%;Iii, 3.4±1.5%;静脉注射38±5%;n = 5)。注射cu - ptsm后10 min,死亡动物肝脏亚细胞部分I、II、III和IV分别含有25±5%、12±3%、17±4%和46±6%的67Cu示踪剂。在静脉注射离子放射性铜(柠檬酸铜)后,在肝脏中发现了相同的67Cu亚细胞分布。注射后10 min,用葡聚糖柱层析进一步分离肝、脑细胞质组分。在肝细胞质中,发现了三种不同的放射性铜组分,分子量约为140,000,41,000-46,000和10,000-16,000 Da。在脑上清部分,大部分放射性铜结合到单一的低分子量细胞质成分(14000 - 16000 Da)。这些结果表明,示踪剂Cu-PTSM的细胞内分解可能导致放射性铜进入正常的细胞铜离子池。
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Subcellular distribution of tissue radiocopper following intravenous administration of 67Cu-labeled Cu-PTSM

The subcellular distribution of radiocopper in the brain and liver of rats has been determined following i.v. administration of Cu-PTSM, pyruvaldehyde bis(N4-methylthiosemicarbazonato)copper(II), labeled with copper-67. Homogenized tissue samples were separated by differential centrifugation into four subcellular fractions: (I) cell membrane + nuclei; (II) mitochondria; (III) microsomes; and (IV) cell cytosol. Upon sacrifice at 10 min post-Cu-PTSM injection, brain fractions, I, II, III and IV contain 35 ± 12, 11 ± 3, 2.8 ± 1.3 and 51 ± 7% of brain activity, respectively (n = 4). In animals sacrificed 24 h post-injection the subcellular fractions of brain tissue show little change from the radiocopper distribution seen at 10 min post-injection, although the mitochondrial fraction may contain slightly more tracer and the cytosolic fraction slightly less (I, 40 ± 10%; II, 18 ± 5%; III, 3.4 ± 1.5%; and IV, 38 ± 5%; n = 5). Subcellular fractions I, II, III and IV of liver contain 25 ± 5, 12 ± 3, 17 ± 4 and 46 ± 6% of 67Cu tracer in animals sacrificed 10 min post-Cu-PTSM injection. An identical subcellular distribution of 67Cu, was found in the liver following i.v. administration of ionic radiocopper (as Cu-citrate). The liver and brain cytosolic fractions at 10 min post-injection were further separated by Sephadex column chromatography. In liver cytosol, three different radiocopper components with molecular weights of about 140,000, 41,000–46,000 and 10,000–16,000 Da were found. In the brain supernatant fraction, most of the radiocopper was bound to a single low molecular weight cytosolic component (14,000–16,000 Da). These results suggest that the intracellular decomposition of tracer Cu-PTSM may result in the radiocopper entering the normal cellular pools for copper ions.

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