Covert J, Splitter G
Department of Animal Health and Biomedical Sciences, University of Wisconsin-Madison 53706, USA.
Vet Immunol Immunopathol. 1995 Nov;49(1-2):39-50. doi: 10.1016/0165-2427(95)05451-b.
Cytokine transcriptional profiles constitute important information about T cell mediated immunity against pathogens. We have developed a reverse transcriptase polymerase chain reaction (RT-PCR) assay to monitor gene expression of bovine T lymphocyte cytokines. Bovine cDNA was reverse transcribed from total RNA and subsequently amplified using primers designed from bovine or murine and human consensus sequences. Cytokine transcription of beta-actin, interleukins (IL) IL-1 alpha, IL-1 beta, IL-2, IL-4, IL-6, IL-10, tumor necrosis factor (TNF)alpha, TNF beta and interferon-gamma was detected from concanavalin A activated peripheral blood mononuclear cells and CD4+ purified T lymphocytes. The assay allows detection of many cytokine mRNA in a species where research has been hindered by lack of commercially available reagents and sequence information. RT-PCR analysis of lymphocyte cytokines will be invaluable for understanding the progression or resolution of disease as a consequence of lymphocyte response to specific antigens.
细胞因子转录谱构成了有关T细胞介导的病原体免疫的重要信息。我们开发了一种逆转录聚合酶链反应(RT-PCR)检测方法来监测牛T淋巴细胞细胞因子的基因表达。从总RNA逆转录得到牛cDNA,随后使用从牛、鼠和人共有序列设计的引物进行扩增。从刀豆蛋白A激活的外周血单个核细胞和CD4 +纯化T淋巴细胞中检测到β-肌动蛋白、白细胞介素(IL)IL-1α、IL-1β、IL-2、IL-4、IL-6、IL-10、肿瘤坏死因子(TNF)α、TNFβ和干扰素-γ的细胞因子转录。该检测方法能够在因缺乏商业试剂和序列信息而阻碍研究的物种中检测多种细胞因子mRNA。淋巴细胞细胞因子的RT-PCR分析对于理解淋巴细胞对特定抗原反应导致的疾病进展或缓解将具有重要价值。