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1,3-双(2-氯乙基)-1-亚硝基脲与地塞米松对大鼠胶质瘤细胞培养物产生的联合生长抑制反应及超微结构改变

Combined growth-inhibitory responses and ultrastructural alterations produced by 1,3-bis(2-chloroethyl)-1-nitrosourea and dexamethasone in rat glioma cell cultures.

作者信息

Grasso R J, Johnson C E, Boler R K, Moore N A

出版信息

Cancer Res. 1977 Feb;37(2):585-94.

PMID:832280
Abstract

The effect of 0.0001 to 10 muM 1,3-bis(2-chloroethyl)-1-nitrosourea (BCNU) and 1 muM dexamethasone on cell proliferation was studied by measuring cell densities in control and drug-treated rat glioma (strain C6) monolayer cultures. When C6 cultures were exposed to 0.01 to 10 muM BCNU, the growth rates decreased for 2 days as control cell populations continued to proliferate at log phase rates. These growth-inhibitory responses were dose dependent and ranged from 20 to 80%, relative to control growth. Subsequently, the growth rates increased and the inhibitory responses ranged from 0 to 12% 4 days later. Cell densities in C6 cultures exposed to 1 muM dexamethasone for 1 day did not differ significantly from controls. Then cell proliferation ceased and the inhibitory response remained at 50% relative to controls in stationary phase. When 0.03 muM BCNU and 1 muM dexamethasone were supplied simultaneously to C6 cultures, a 35% inhibitory response occurred after 1 day. This response did not differ significantly from that observed with 0.03 muM BCNU alone. After 4 days, the inhibitory response did not decrease in cultures containing both drugs, but did decrease to 13% in the 0.03 muM BCNU-treated cultures. In 1 muM BCNU-treated cultures, the response was 66% after 1 day, which decreased to 21% 5 days later. When 1 muM BCNU was supplied to C6 cultures that were pretreated for 1 day with 1 muM dexamethasone, the response was 91% the following day, and this decreased to only 54% 5 days later. Dose-response curves showed that the inhibitory responses after 1 day in these pretreated cultures exposed to 0.001 to 10 muM BCNU increased up to 22% relative to the responses produced by either drug alone. After 5 days, the responses in the pretreated cultures exposed to 0.001 to 1 muM BCNU was 50%, which was similar to the response produced by 1 muM dexamethasone alone. Ultrastructural studies revealed that control and 1 muM BCNU-treated C6 cells contained 18 mitochondria, but the treated cells were 10% smaller after 1 day. Cells exposed to 1 muM dexamethasone for 1 day conount of granular endoplasmic reticulum increased greater than 80% in cells treated with BCNU for 1 day or dexamethasone for 2 days. C6 cells pretreated with dexamethasone and exposed to BCNU for an additional day (a) contained 23 mitochondria, (b) did not decrease in size, and (c) exhibited a greater than 250% increase in the amount of granular endoplasmic reticulum. These results demonstrate that combined growth-inhibitory responses and ultrastructural alterations occur when C6 cells are treated sequentially with 1 muM dexamethasone and BCNU.

摘要

通过测量对照和药物处理的大鼠胶质瘤(C6 株)单层培养物中的细胞密度,研究了 0.0001 至 10 μM 的 1,3 - 双(2 - 氯乙基)-1 - 亚硝基脲(BCNU)和 1 μM 地塞米松对细胞增殖的影响。当 C6 培养物暴露于 0.01 至 10 μM 的 BCNU 时,随着对照细胞群体以对数期速率持续增殖,生长速率在 2 天内下降。这些生长抑制反应呈剂量依赖性,相对于对照生长,范围为 20%至 80%。随后,生长速率增加,4 天后抑制反应范围为 0%至 12%。暴露于 1 μM 地塞米松 1 天的 C6 培养物中的细胞密度与对照无显著差异。然后细胞增殖停止,相对于静止期的对照,抑制反应保持在 50%。当将 0.03 μM BCNU 和 1 μM 地塞米松同时加入 C6 培养物时,1 天后出现 35%的抑制反应。该反应与单独使用 0.03 μM BCNU 时观察到的反应无显著差异。4 天后,含两种药物的培养物中的抑制反应没有降低,但在 0.03 μM BCNU 处理的培养物中降至 13%。在 1 μM BCNU 处理的培养物中,1 天后反应为 66%,5 天后降至 21%。当将 1 μM BCNU 加入预先用 1 μM 地塞米松处理 1 天的 C6 培养物中时,第二天反应为 91%,5 天后仅降至 54%。剂量反应曲线表明,在这些预先处理的培养物中,暴露于 0.001 至 10 μM BCNU 1 天后的抑制反应相对于单独使用任何一种药物产生的反应增加高达 22%。5 天后,暴露于 0.001 至 1 μM BCNU 的预先处理培养物中的反应为 50%,这与单独使用 1 μM 地塞米松产生的反应相似。超微结构研究表明,对照和 1 μM BCNU 处理的 C6 细胞含有 18 个线粒体,但处理后的细胞在 1 天后小 10%。暴露于 1 μM 地塞米松 1 天的细胞,其颗粒内质网的数量增加超过 80%,而在 BCNU 处理 1 天或地塞米松处理 2 天的细胞中也是如此。预先用地塞米松处理并再暴露于 BCNU 1 天的 C6 细胞:(a)含有 23 个线粒体;(b)大小没有减小;(c)颗粒内质网的数量增加超过 250%。这些结果表明,当 C6 细胞先后用 1 μM 地塞米松和 BCNU 处理时,会出现联合生长抑制反应和超微结构改变。

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