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B细胞激活与耐受的淋巴瘤模型。VIII. sIgM和sIgD的交叉脱敏作用及其对抗同种型抗体调节生长的影响。

Lymphoma models for B cell activation and tolerance. VIII. Cross-desensitization by sIgM and sIgD and its effects on growth regulation by anti-isotype antibodies.

作者信息

Alés-Martínez J E, Warner G L, Scott D W

机构信息

Immunology Unit, University of Rochester School of Medicine and Dentistry, New York 14642.

出版信息

Cell Immunol. 1990 May;127(2):527-34. doi: 10.1016/0008-8749(90)90153-i.

DOI:10.1016/0008-8749(90)90153-i
PMID:2328538
Abstract

ECH408-1 is a murine B cell lymphoma expressing idiotypically and allotypically distinguishable transfected and endogenous IgD. Previously, we demonstrated that this cell line was not growth inhibited by antibodies directed at membrane IgD, but could be inhibited by antibodies which crosslink membrane IgM. Herein, we demonstrate that both anti-mu and anti-delta will cause calcium mobilization in this transfected cell line; this is followed by a period during which antibodies against the alternative isotype are unable to induce significant increases in intracellular calcium concentrations. This phenomenon, called "desensitization," is short-lived, lasting 20 min. We further demonstrate that acute desensitization of these cells by anti-delta has no effect on immediate growth inhibition which is elicited by anti-mu. These data confirm our earlier proposal that the rapid, initial calcium response seen in these lymphomas is not required for the negative signal for growth. Moreover, we also demonstrate that pretreatment of these lymphoma cells with phorbol myristate acetate (PMA) also renders these lymphoma cells temporarily incapable of manifesting a significant calcium signal. Nonetheless, PMA-pretreated B lymphoma cells are not altered in their subsequent sensitivity to anti-mu growth inhibition, nor are they affected in their resistance to inhibition by anti-delta. Our data confirm the proposal that neither the calcium signal nor protein kinase-C activation is involved in the modulation of B lymphoma growth.

摘要

ECH408-1是一种鼠B细胞淋巴瘤,表达具有独特型和同种异型可区分的转染和内源性IgD。此前,我们证明该细胞系不受针对膜IgD的抗体抑制生长,但可被交联膜IgM的抗体抑制。在此,我们证明抗μ和抗δ抗体均可在该转染细胞系中引起钙动员;随后会有一段时间,针对另一种同种型的抗体无法诱导细胞内钙浓度显著升高。这种现象称为“脱敏”,持续时间较短,为20分钟。我们进一步证明,抗δ对这些细胞的急性脱敏对抗μ引发的即时生长抑制没有影响。这些数据证实了我们之前的推测,即这些淋巴瘤中快速的初始钙反应对于生长的负信号并非必需。此外,我们还证明用佛波酯肉豆蔻酸酯(PMA)预处理这些淋巴瘤细胞也会使它们暂时无法表现出显著的钙信号。尽管如此,PMA预处理的B淋巴瘤细胞对抗μ生长抑制的后续敏感性并未改变,对抗δ抑制的抗性也未受影响。我们的数据证实了既没有钙信号也没有蛋白激酶-C激活参与B淋巴瘤生长调节的推测。

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