Franz A, Bryant A, Farrant J
Immunodeficiency Diseases Research Group, Clinical Research Centre, Harrow, U.K.
Immunology. 1991 Jul;73(3):322-6.
Responses to interleukin-2 (IL-2) of high-density human tonsillar B lymphocytes were examined in 20 microliters hanging drop microcultures. DNA synthesis and secretion of IgM and IgG were induced by IL-2 alone. Activation of calcium-dependent protein kinase C (PKC) with phorbol 12,13-dibutyrate and ionomycin increased IL-2 driven DNA synthesis yet reduced IL-2 driven secretion of IgM and IgG. Forskolin, which increases cAMP, had no effect on the responses to IL-2. Intrinsic IL-6 played no role in IL-2-induced DNA synthesis but was partially responsible for the secretion of immunoglobulin. These data show that pre-activation of the high-density human tonsillar B lymphocyte is not a prerequisite for IL-2-driven responses. They also show an asymmetry between the growth and differentiation induced by IL-2. This is reflected by opposite modulation on activation of PKC and by the role of the autocrine factor, IL-6.
在20微升悬滴微培养体系中检测了高密度人扁桃体B淋巴细胞对白介素-2(IL-2)的反应。单独的IL-2可诱导DNA合成以及IgM和IgG的分泌。用佛波酯12,13 - 二丁酸酯和离子霉素激活钙依赖性蛋白激酶C(PKC)可增加IL-2驱动的DNA合成,但会减少IL-2驱动的IgM和IgG分泌。可增加cAMP的福斯高林对IL-2诱导的反应没有影响。内源性IL-6在IL-2诱导的DNA合成中不起作用,但部分参与免疫球蛋白的分泌。这些数据表明,高密度人扁桃体B淋巴细胞的预激活不是IL-2驱动反应的先决条件。它们还显示了IL-2诱导的生长和分化之间的不对称性。这通过对PKC激活的相反调节以及自分泌因子IL-6的作用得以体现。