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呼吸道细胞对伽马射线的相对致断裂敏感性

Comparative clastogenic sensitivity of respiratory tract cells to gamma rays.

作者信息

Bao S, Harwood P W, Wood B H, Chrisler W B, Groch K M, Brooks A L

机构信息

United States Transuranium and Uranium Registries, Washington State University, Richland 99352, USA.

出版信息

Radiat Res. 1997 Jul;148(1):90-7.

PMID:9216622
Abstract

To understand the relationships between exposure and damage to different cell populations in the respiratory tract, methods were developed to culture deep-lung fibroblasts and epithelial cells from the nose, trachea and deep lungs. Female F-344 Fischer and male Wistar rats were exposed to 1-5 Gy of 60Co gamma rays at a dose rate of 0.4 Gy/min. Cells were isolated for short-term culture, and the incidences of binucleated cells and micronuclei were determined. The incidences of micronuclei were determined in cytochalasin-B-induced binucleated cells at 72 h for nasal and tracheal tissue and 96 h for deep-lung fibroblasts and epithelial cells. Maximum frequencies of binucleated cells were found in the control nonirradiated cells at these harvest times, and the frequencies were not significantly affected at these harvest times by radiation exposure. No significant differences were found in the frequencies of micronuclei induced in the nasal epithelial cells isolated from female F-344 Fischer or male Wistar rats. Fibroblasts cultured in different media and isolated from either female F-344 Fischer or male Wistar rats also showed a similar frequency of micronuclei. Over the doses tested, the frequency of micronuclei in the respiratory tract cells increased linearly with the dose. The slopes were 92.2 +/- 9.2, 76.2 +/- 7.9, 32.8 +/- 2.4 and 28.7 +/- 3.4 micronuclei/1000 binucleated cells/Gy for deep-lung epithelial cells, deep-lung fibroblasts, tracheal epithelial cells and nasal epithelial cells, respectively. Deep-lung epithelial or fibroblast cells were about two to three times as sensitive for elastogenic damage as nasal and tracheal epithelial cells. The measurement of micronuclei in isolated respiratory tract cells is very useful in assessing cytogenetic damage induced in different cell types by radiation.

摘要

为了解呼吸道中不同细胞群体的暴露与损伤之间的关系,人们开发了从鼻腔、气管和深部肺组织培养深部肺成纤维细胞和上皮细胞的方法。将雌性F-344费希尔大鼠和雄性Wistar大鼠以0.4 Gy/min的剂量率暴露于1-5 Gy的60Coγ射线。分离细胞进行短期培养,并测定双核细胞和微核的发生率。在细胞松弛素B诱导的双核细胞中,于72小时测定鼻腔和气管组织的微核发生率,于96小时测定深部肺成纤维细胞和上皮细胞的微核发生率。在这些收获时间,对照未照射细胞中双核细胞的频率最高,且这些收获时间的辐射暴露对频率没有显著影响。从雌性F-344费希尔大鼠或雄性Wistar大鼠分离的鼻腔上皮细胞中诱导的微核频率没有显著差异。在不同培养基中培养且从雌性F-344费希尔大鼠或雄性Wistar大鼠分离的成纤维细胞也显示出相似的微核频率。在所测试的剂量范围内,呼吸道细胞中的微核频率随剂量呈线性增加。深部肺上皮细胞、深部肺成纤维细胞、气管上皮细胞和鼻腔上皮细胞的斜率分别为92.2±9.2、76.2±7.9、32.8±2.4和28.7±3.4微核/1000双核细胞/Gy。深部肺上皮或成纤维细胞对弹性损伤的敏感性约为鼻腔和气管上皮细胞的两到三倍。在分离的呼吸道细胞中测量微核对于评估辐射在不同细胞类型中诱导的细胞遗传损伤非常有用。

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