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微小棒状杆菌刺激的脾集落形成单位(CFU-S)放射敏感性的早期变化

Early changes in the radiosensitivity of Corynebacterium parvum-stimulated CFU-S.

作者信息

Maruyama Y, Grider C

出版信息

Stem Cells (1981). 1981;1(2):81-96.

PMID:7348462
Abstract

Corynebacterium parvum injected intraperitoneally into C57BL mice induced a progression of hemopoietic CFU-S of C57BL mice from the resting state immediately after, and in the early period (approximately 8 h) after stimulation. Dose-response survival curves of the stimulated endogenous spleen CFU-S after the C. parvum injection revealed changing slopes or D0 of dose-response survival curves indicative of changing sensitivity states. Shortly after stimulation, the cells were sensitive to high specific-activity tritiated thymidine (HSATT) or hydroxyurea (HU), indicating they were in the DNA-S phase. This commenced shortly after the C. parvum injection. Beginning at about 6 h, sensitivity to HSATT disappeared and there was an increase in radiosensitivity. Sensitivity to vinblastine (VLB) also became evident at 7 h. This was consistent with beginning mitosis and mitotic cell sensitivity to VLB. A dose-response survival curve for the G2 phase CFU-S was determined using both HSATT and VLB to eliminate the DNA-S phase and mitotic cells. The radiosensitivities of the resting G1, S, and G1-S phase cells were determined by D0 to be 80, 105 and 85 rad, respectively, measured in vivo. G2 sensitivity using a combined HSATT and VLB method showed a complex, bending dose-response curve with a terminal D0 of 58 rad. CFU-S progression was blocked by the anti-histamine H2 receptor agent, metiamide.

摘要

腹腔注射微小棒状杆菌给C57BL小鼠,可诱导C57BL小鼠造血CFU-S从静息状态开始,并在刺激后的早期阶段(约8小时)发生进展。注射微小棒状杆菌后,受刺激的内源性脾CFU-S的剂量-反应存活曲线显示出剂量-反应存活曲线的斜率或D0发生变化,表明敏感性状态发生改变。刺激后不久,细胞对高比活度氚标记胸腺嘧啶核苷(HSATT)或羟基脲(HU)敏感,表明它们处于DNA合成期。这在注射微小棒状杆菌后不久就开始了。大约在6小时后,对HSATT的敏感性消失,放射敏感性增加。对长春碱(VLB)的敏感性在7小时时也变得明显。这与开始有丝分裂以及有丝分裂细胞对VLB的敏感性一致。使用HSATT和VLB来消除DNA合成期和有丝分裂细胞,从而确定了G2期CFU-S的剂量-反应存活曲线。通过D0测定,静息G1期、S期和G1-S期细胞的放射敏感性在体内分别为80、105和85拉德。使用HSATT和VLB联合方法测定的G2期敏感性显示出一条复杂的、弯曲的剂量-反应曲线,其末端D0为58拉德。CFU-S的进展被抗组胺H2受体药物甲硫米特阻断。

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