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比较七种促细胞分裂剂与植物血凝素-M在双着丝粒染色体分析生物剂量测定中对淋巴细胞刺激的改善情况。

Comparing seven mitogens with PHA-M for improved lymphocyte stimulation in dicentric chromosome analysis for biodosimetry.

作者信息

Beinke C, Port M, Lamkowski A, Abend M

机构信息

Bundeswehr Institute of Radiobiology Affiliated to the University Ulm, Neuherbergstr. 11, Munich 80937, Germany

Bundeswehr Institute of Radiobiology Affiliated to the University Ulm, Neuherbergstr. 11, Munich 80937, Germany.

出版信息

Radiat Prot Dosimetry. 2016 Feb;168(2):235-41. doi: 10.1093/rpd/ncv286. Epub 2015 May 9.

Abstract

Dicentric chromosome analysis (DCA) is the gold standard for individual radiation dose estimation. Two limiting factors of DCA are the time-consuming lymphocyte stimulation and proliferation using the lectin PHA-M and the upper dose limit of individual dose assessment of ∼4 Gy. By measuring the mitotic index (MI), the authors investigated systematically whether the stimulation of lymphocytes can be improved after administration of alternative (and combined) mitogens. The authors compared the lymphocyte stimulation effectiveness of the traditionally used PHA-M (from Phaseolus vulgaris) with seven cited mitogens by determination of MIs: five lectins namely CNA (concanavalin A), PW (pokeweed), LMA (Maackia amurensis), LTV (T. vulgaris), PHA-L (P. vulgaris) as well as LPS (lipopolysaccharide, Escherichia coli) and SLO (streptolysine O, Streptococcus pyogenes) were applied. The conventional protocol using PHA-M for lymphocyte stimulation proved to be superior over lower/higher PHA-M concentrations as well as seven other mitogens administered either alone or combined with SLO or LPS.

摘要

双着丝粒染色体分析(DCA)是个体辐射剂量估计的金标准。DCA的两个限制因素是使用凝集素PHA - M进行淋巴细胞刺激和增殖耗时,以及个体剂量评估的上限约为4 Gy。通过测量有丝分裂指数(MI),作者系统地研究了在施用替代(和联合)促细胞分裂剂后淋巴细胞刺激是否可以得到改善。作者通过测定MI,将传统使用的PHA - M(来自菜豆)与七种引用的促细胞分裂剂的淋巴细胞刺激效果进行了比较:应用了五种凝集素,即刀豆球蛋白A(CNA)、商陆(PW)、山槐凝集素(LMA)、普通豌豆凝集素(LTV)、菜豆凝集素(PHA - L),以及脂多糖(LPS,来自大肠杆菌)和链球菌溶血素O(SLO,来自化脓性链球菌)。事实证明,使用PHA - M进行淋巴细胞刺激的传统方案优于较低/较高浓度的PHA - M以及单独或与SLO或LPS联合使用的其他七种促细胞分裂剂。

相似文献

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本文引用的文献

1
A new model of biodosimetry to integrate low and high doses.一种整合低剂量和高剂量的生物剂量测定新模型。
PLoS One. 2014 Dec 2;9(12):e114137. doi: 10.1371/journal.pone.0114137. eCollection 2014.
2
Realising the European network of biodosimetry: RENEB-status quo.实现欧洲生物剂量测定网络:RENE B的现状。
Radiat Prot Dosimetry. 2015 Apr;164(1-2):42-5. doi: 10.1093/rpd/ncu266. Epub 2014 Sep 9.
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