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类器官培养中照射后大鼠乳腺克隆原细胞潜在致死性损伤的修复

Repair of potentially lethal damage in rat mammary clonogens following irradiation in organoid culture.

作者信息

Kamiya K, Kim N D, Gould M N, Clifton K H

机构信息

Department of Human Oncology, University of Wisconsin Clinical Cancer Center, Madison.

出版信息

Int J Radiat Biol. 1991 May;59(5):1207-16. doi: 10.1080/09553009114551081.

Abstract

In the course of investigations of radiogenic neoplasia in mammary cells in vivo, post-irradiation repair of potentially lethal damage (PLDR) was previously observed in mammary epithelial clonogens when they were irradiated and left in their tissue environment for 4-24 h after exposure. This type of PLDR increases the initial shoulder of the survival curve without significantly affecting its terminal slope. It has since been described in similarly treated thyroid and hepatic clonogens, and significantly exceeds that generally seen in most mammalian cells in culture. In this study, a ten-fold increase in the concentration of mammary clonogens which could be assayed was achieved by the isolation and short term culture (2-4 days) of mammary organoids (ductal and end-bud fragments). Assays of clonogen concentrations were carried out with cell suspensions prepared immediately following irradiation of 4-day organoid cultures or 24 h after irradiation of such organoid cultures. A near four-fold increase in clonogen survival was observed with the delay in assay after irradiation; this is comparable to the PLDR seen in mammary clonogens irradiated and left in situ for 4-24 h after exposure.

摘要

在对体内乳腺细胞放射性肿瘤形成的研究过程中,之前观察到,当乳腺上皮克隆原受到照射并在照射后于其组织环境中放置4至24小时时,潜在致死性损伤(PLDR)的照射后修复现象。这种类型的PLDR增加了存活曲线的初始肩部,而对其终末斜率没有显著影响。此后,在经过类似处理的甲状腺和肝克隆原中也有描述,并且明显超过了大多数培养的哺乳动物细胞中通常所见的情况。在本研究中,通过分离和短期培养(2至4天)乳腺类器官(导管和终末芽片段),可检测的乳腺克隆原浓度增加了10倍。克隆原浓度测定是在4天类器官培养物照射后立即制备的细胞悬液或此类类器官培养物照射后24小时进行的。照射后延迟测定观察到克隆原存活率增加了近4倍;这与照射后留在原位4至24小时的乳腺克隆原中所见的PLDR相当。

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