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低剂量辐射诱导的免疫调节:对巨噬细胞和CD8 + T细胞的影响。

Low dose radiation induced immunomodulation: effect on macrophages and CD8+ T cells.

作者信息

Pandey Ruchi, Shankar Bhavani S, Sharma Deepak, Sainis Krishna B

机构信息

Radiation Biology and Health Sciences Division, Bioscience Group, Bhabha Atomic Research Centre, Modular Laboratories, Trombay, Mumbai, India.

出版信息

Int J Radiat Biol. 2005 Nov;81(11):801-12. doi: 10.1080/09553000500531886.

Abstract

PURPOSE

The aim of the present investigation was to study the effect of fractionated whole body low dose ionizing radiation (LDR) on the functional responses of T lymphocytes, their subpopulations and macrophages.

MATERIALS AND METHODS

C57BL/6 mice were exposed to 4 cGy from a (60)Co source, at 0.31 cGy/min, at 24 h intervals for 5 days (total dose 20 cGy). Phagocytic activity was measured by flow cytometry using Bioparticles and nitric oxide generation was estimated by spectrophotometry. Proliferation of lymphocytes in response to concanavalin A (con A) and alloantigens was measured by (3)H thymidine incorporation. Expression of cell surface markers was assessed by flow cytometric analysis of antibody labeled cells. Target cell killing by cytotoxic T cells (CTL) generated against allogenic cells was assessed by flow cytometry using PKH26 labeled target cells. Cytokines were estimated by enzyme linked immunosorbent assay.

RESULTS

Exposure to LDR enhanced nitric oxide secretion and phagocytosis. The expression of early activation antigen, CD69, was enhanced in CD8(+) T lymphocytes concomitant with enhanced proliferation in response to con A. In addition, mixed lymphocyte reaction (MLR) and CTL response were augmented and secretion of interferon gamma (IFN-gamma) was suppressed following LDR exposure.

CONCLUSIONS

LDR exposure enhanced the function of macrophages and responses of CD8(+) T cells in C57BL/6 mice.

摘要

目的

本研究旨在探讨分次全身低剂量电离辐射(LDR)对T淋巴细胞及其亚群和巨噬细胞功能反应的影响。

材料与方法

C57BL/6小鼠接受来自(60)Co源的4 cGy辐射,剂量率为0.31 cGy/分钟,每隔24小时照射一次,共照射5天(总剂量20 cGy)。使用生物颗粒通过流式细胞术测量吞噬活性,并通过分光光度法估计一氧化氮的产生。通过(3)H胸苷掺入法测量淋巴细胞对刀豆球蛋白A(con A)和同种异体抗原的增殖反应。通过对抗体标记细胞的流式细胞术分析评估细胞表面标志物的表达。使用PKH26标记的靶细胞通过流式细胞术评估针对同种异体细胞产生的细胞毒性T细胞(CTL)对靶细胞的杀伤作用。通过酶联免疫吸附测定法估计细胞因子。

结果

暴露于LDR可增强一氧化氮分泌和吞噬作用。CD8(+)T淋巴细胞中早期活化抗原CD69的表达增强,同时对con A的增殖反应增强。此外,LDR暴露后混合淋巴细胞反应(MLR)和CTL反应增强,干扰素γ(IFN-γ)分泌受到抑制。

结论

LDR暴露增强了C57BL/6小鼠巨噬细胞的功能和CD8(+)T细胞的反应。

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