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锝-99m-替曲膦、锝-99m-甲氧基异丁基异腈和铊-201在肿瘤细胞系中的摄取情况。

Uptake of technetium-99m-tetrofosmin, technetium-99m-MIBI and thallium-201 in tumor cell lines.

作者信息

Arbab A S, Koizumi K, Toyama K, Araki T

机构信息

Department of Radiology, Yamanashi Medical University, Japan.

出版信息

J Nucl Med. 1996 Sep;37(9):1551-6.

PMID:8790217
Abstract

UNLABELLED

We investigated the kinetics, cellular uptake and intracellular distribution of 99mTc-tetrofosmin in tumor cell lines and compared them with those of 99mTc-MIBI and 201TI.

METHODS

At specific intervals after incubation with radiotracers, cellular uptake was determined. Cells were also treated with nigericin, carbonyl cyanide m-chloro-phenylhydrazone (CCCP) and ouabain to determine their effects on the uptake of the tracers.

RESULTS

Each tracer showed similar uptake kinetics in both cell lines, and a steady-state was maintained for at least 4 hr. Nigericin stimulated the uptake of both 99mTc-tetrofosmin and 99mTc-MIBI in HBL-2 cells, although it inhibited their uptake in SW-13 cells. Nigericin also inhibited 90% of 201TI uptake in both cell lines. Addition of CCCP caused 73%-97% release of accumulated 99mTc-MIBI from both cell lines with or without nigericin pretreatment, indicating that most of the accumulated 99mTc-MIBI was related to mitochondria. The effect of CCCP on accumulated 99mTc-tetrofosmin was less marked than that on 99mTc-MIBI in both cell lines, indicating that only a part of accumulated 99mTc-tetrofosmin, was related to mitochondria. Ouabain preincubation inhibited 74%-77% and 51%-53% of 201TI uptake in HBL-2 and SW-13 cells, respectively, as well as inhibited 22%-31% uptake of 99mTc-tetrofosmin in both HBL-2 and SW-13 cells. Uptake by the dead cells of either cell line was negligible for each tracer.

CONCLUSION

Technetium-99m-tetrofosmin uptake depends on both cell membrane and mitochondrial potentials. Only a small fraction of 99mTc-tetrofosmin accumulates inside the mitochondria, while most 99mTc-MIBI accumulates inside the mitochondria. Thallium-201 uptake is partly independent of the Na+, K+ pump.

摘要

未标记

我们研究了99mTc-替曲膦在肿瘤细胞系中的动力学、细胞摄取和细胞内分布,并将其与99mTc-MIBI和201Tl的情况进行了比较。

方法

在与放射性示踪剂孵育后的特定时间间隔,测定细胞摄取情况。还用尼日利亚菌素、羰基氰化物间氯苯腙(CCCP)和哇巴因处理细胞,以确定它们对示踪剂摄取的影响。

结果

每种示踪剂在两种细胞系中均显示出相似的摄取动力学,并且至少4小时内维持稳态。尼日利亚菌素刺激了HBL-2细胞对99mTc-替曲膦和99mTc-MIBI的摄取,尽管它抑制了SW-13细胞中它们的摄取。尼日利亚菌素在两种细胞系中还抑制了90%的201Tl摄取。添加CCCP导致无论有无尼日利亚菌素预处理,两种细胞系中积累的99mTc-MIBI有73%-97%释放,这表明大部分积累的99mTc-MIBI与线粒体有关。在两种细胞系中,CCCP对积累的99mTc-替曲膦的影响比对99mTc-MIBI的影响小,这表明积累的99mTc-替曲膦只有一部分与线粒体有关。哇巴因预孵育分别抑制了HBL-2和SW-13细胞中74%-77%和51%-53%的201Tl摄取,以及HBL-2和SW-13细胞中22%-31%的99mTc-替曲膦摄取。每种示踪剂在任一细胞系的死细胞中的摄取都可忽略不计。

结论

99mTc-替曲膦的摄取取决于细胞膜和线粒体电位。只有一小部分99mTc-替曲膦在线粒体内积累,而大部分99mTc-MIBI在线粒体内积累。201Tl的摄取部分独立于Na+、K+泵。

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