Käser Tobias, Gerner Wilhelm, Hammer Sabine E, Patzl Martina, Saalmüller Armin
Department of Pathobiology, University of Veterinary Medicine Vienna, Veterinärplatz 1, 1210 Vienna, Austria.
Vet Immunol Immunopathol. 2008 Sep 15;125(1-2):92-101. doi: 10.1016/j.vetimm.2008.05.007. Epub 2008 May 16.
Regulatory T cells (Tregs) are potent regulators of various immune reactions. Due to the lack of Treg-specific markers their analysis had often been challenging until the discovery of the transcription factor Forkhead-box p3 (Foxp3) which serves as this highly demanded marker. So far, antibodies staining human and murine Foxp3 have been developed. This study describes the analysis of four commercially available anti-Foxp3 antibodies for reactivity with their specific antigen in cells derived from porcine lymphoid tissues. One out of the four antibodies showed selective reactivity with porcine CD25(+) T lymphocytes. The intracellular antigen was expressed on a small subset of CD25(dim) cells and the majority of the CD25(high) positive T-cell subpopulation. Intracellular antigen positive cells showed a heterogeneous expression of other leukocyte differentiation antigens. The majority belonged to the CD4(+)CD8(+) T-lymphocyte subpopulation, but were also found in the CD4(+)CD8(-) subpopulation. Another small minority was included in the CD4(-)CD8(+) T-lymphocyte subpopulation. Additionally, a small fraction of the putative Foxp3(+) cells showed an expression of MHC-II molecules. These staining patterns in three and four colour flow cytometry analyses indicated that the cells detected by a rat anti-mouse/rat-Foxp3 antibody expressed the porcine Foxp3. The expression of the putative Foxp3 protein in distinct leukocyte subsets was confirmed by molecular analysis of Foxp3 mRNA expression. Using Western blot analysis specific protein bands could only be detected in fractions that also exhibited the corresponding Foxp3 mRNA expression. These experiments also revealed that the antibody recognized a single chain protein with a molecular mass of about 45kDA similar to Foxp3 described for other species. In summary, these data strongly indicate the reactivity of this antibody with porcine Foxp3. Thereby, this rat anti-mouse/rat Foxp3 antibody presents a powerful tool for the identification of porcine regulatory T cells.
调节性T细胞(Tregs)是各种免疫反应的有效调节者。由于缺乏Treg特异性标志物,在转录因子叉头框p3(Foxp3)被发现之前,对它们的分析一直具有挑战性,而Foxp3可作为这种急需的标志物。到目前为止,已经开发出了可对人和小鼠Foxp3进行染色的抗体。本研究描述了对四种市售抗Foxp3抗体在源自猪淋巴组织的细胞中与它们的特异性抗原反应性的分析。四种抗体中的一种显示出与猪CD25(+) T淋巴细胞具有选择性反应性。细胞内抗原在一小部分CD25(dim)细胞以及大多数CD25(high)阳性T细胞亚群上表达。细胞内抗原阳性细胞显示出其他白细胞分化抗原的异质性表达。大多数属于CD4(+)CD8(+) T淋巴细胞亚群,但在CD4(+)CD8(-)亚群中也有发现。另一个小的少数群体包含在CD4(-)CD8(+) T淋巴细胞亚群中。此外,一小部分假定的Foxp3(+)细胞显示出MHC-II分子的表达。这些在三色和四色流式细胞术分析中的染色模式表明,由大鼠抗小鼠/大鼠Foxp3抗体检测到的细胞表达了猪Foxp3。通过对Foxp3 mRNA表达的分子分析证实了假定的Foxp3蛋白在不同白细胞亚群中的表达。使用蛋白质印迹分析,仅在也表现出相应Foxp3 mRNA表达的组分中检测到特异性蛋白条带。这些实验还表明,该抗体识别一种分子量约为45kDa的单链蛋白,类似于其他物种中描述的Foxp3。总之,这些数据有力地表明了该抗体与猪Foxp3的反应性。因此,这种大鼠抗小鼠/大鼠Foxp3抗体是鉴定猪调节性T细胞的有力工具。