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细胞代谢比色法用于评估CD4⁺T细胞增殖的适用性:与5-溴-2-脱氧尿苷(BrdU)酶联免疫吸附测定法的比较

Suitability of cell metabolic colorimetric assays for assessment of CD4+ T cell proliferation: comparison to 5-bromo-2-deoxyuridine (BrdU) ELISA.

作者信息

Maghni K, Nicolescu O M, Martin J G

机构信息

Meakins-Christie Laboratories, McGill University, Montreal, Quebec, Canada.

出版信息

J Immunol Methods. 1999 Mar 4;223(2):185-94. doi: 10.1016/s0022-1759(98)00220-8.

Abstract

The conventional tritiated thymidine (3H-TdR) incorporation assay is considered as the 'gold standard' for the assessment of cell growth. However, the 3H-TdR incorporation assay has several disadvantages which have prompted the development of nonradiolabelling proliferation assays such as 5-bromo-2-deoxyuridine (BrdU) ELISA, tetrazolium microplate assay and acid phosphatase assay. In studies, these three proliferation assays have shown equivalent sensitivity and reproducibility to the 3H-TdR incorporation assay. However the results may be affected by the cell type studied. In the present study, we have used these three proliferation assays for the assessment of rat lymph node CD4 + T lymphocyte growth in response to polyclonal antigen stimulation. The proliferation assays were compared on the basis of four criteria: sensitivity, reproducibility, stimulation index and insensitivity of the assay to the cell number. Our results indicated that the BrdU ELISA demonstrated the highest sensitivity, reproducibility and stimulation index but had a limited linear range for cellular growth. The tetrazolium microplate assay also had a relatively good sensitivity, reproducibility, stimulation index and a wider linear response range for cell growth in comparison to the BrdU ELISA. The acid phosphatase assay showed the lowest reproducibility and stimulation index. Because BrdU incorporation in DNA of proliferating cells has been reported to block cell division, we have investigated this possibility in sequential assays. Our results indicated that in our experimental conditions no evidence of an anti-mitogenic action of BrdU was observed. We also compared the performance of the MTS assay and BrdU ELISA in measuring substance P-induced CD4 + T cell proliferation. The results indicated that the MTS assay may reflect change in cell activation leading to an overestimate of cell growth. In conclusion, our results indicate that the BrdU ELISA is the most sensitive of the three proliferation assays used for the assessment of CD4 + T lymphocyte growth and is the preferred assay when small changes in cell growth are expected.

摘要

传统的氚标记胸腺嘧啶核苷(3H-TdR)掺入试验被视为评估细胞生长的“金标准”。然而,3H-TdR掺入试验存在若干缺点,这促使了非放射性标记增殖试验的发展,如5-溴-2-脱氧尿苷(BrdU)酶联免疫吸附测定、四唑盐微孔板测定和酸性磷酸酶测定。在研究中,这三种增殖试验已显示出与3H-TdR掺入试验相当的敏感性和可重复性。然而,结果可能会受到所研究细胞类型的影响。在本研究中,我们使用这三种增殖试验来评估大鼠淋巴结CD4 + T淋巴细胞在多克隆抗原刺激下的生长情况。基于四个标准对增殖试验进行了比较:敏感性、可重复性、刺激指数以及试验对细胞数量的不敏感性。我们的结果表明,BrdU酶联免疫吸附测定显示出最高的敏感性、可重复性和刺激指数,但细胞生长的线性范围有限。与BrdU酶联免疫吸附测定相比,四唑盐微孔板测定在细胞生长方面也具有相对较好的敏感性、可重复性、刺激指数和更宽的线性响应范围。酸性磷酸酶测定显示出最低的可重复性和刺激指数。由于据报道增殖细胞DNA中BrdU的掺入可阻断细胞分裂,我们在连续试验中研究了这种可能性。我们的结果表明,在我们的实验条件下,未观察到BrdU具有抗有丝分裂作用的证据。我们还比较了MTS测定和BrdU酶联免疫吸附测定在测量P物质诱导的CD4 + T细胞增殖方面的性能。结果表明,MTS测定可能反映细胞活化的变化,从而导致对细胞生长的高估。总之,我们的结果表明,BrdU酶联免疫吸附测定是用于评估CD4 + T淋巴细胞生长的三种增殖试验中最敏感的,并且在预期细胞生长有微小变化时是首选试验。

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