Buttke T M, Mallett G S, Cuchens M A
J Immunol Methods. 1983 Mar 11;58(1-2):193-207. doi: 10.1016/0022-1759(83)90275-2.
Mouse spleen cells were separated into Ig+ and Ig- populations by positive selection using petri plates coated with rabbit anti-mouse immunoglobulin. The Ig- cells were subsequently incubated with mouse monoclonal alloantisera to Thy1.2 prior to a second positive selection. The adherent populations were characterized as B (Ig+) or T (Thy1.2+) lymphocytes on the basis of surface immunofluorescence and mitogen-induced proliferation. Analysis of the 2 isolated populations by flow cytometry showed that B and T lymphocytes could be distinguished by their forward light scatter as well as their fluorescence after incubation with fluorescein diacetate.
通过使用包被有兔抗小鼠免疫球蛋白的培养皿进行阳性选择,将小鼠脾细胞分离为Ig⁺和Ig⁻群体。随后,在第二次阳性选择之前,将Ig⁻细胞与小鼠抗Thy1.2单克隆同种抗血清一起孵育。根据表面免疫荧光和丝裂原诱导的增殖情况,将贴壁群体鉴定为B(Ig⁺)或T(Thy1.2⁺)淋巴细胞。通过流式细胞术对这两个分离群体进行分析表明,B淋巴细胞和T淋巴细胞可以通过前向光散射以及与二乙酸荧光素孵育后的荧光来区分。