Hasbold J, Klaus G G
National Institute for Medical Research, Mill Hill, London, GB.
Eur J Immunol. 1990 Aug;20(8):1685-90. doi: 10.1002/eji.1830200810.
WEHI-231 and CH31 are phenotypically immature sIgM+ murine B cell lymphomas whose growth is inhibited by anti-immunoglobulin (Ig) antibodies. These lines have therefore been used as models for studying the role of surface Ig receptors in the induction of B cell tolerance. We show here that anti-mu antibodies induce DNA cleavage into oligonucleosomal fragments characteristic of programmed cell death (apoptosis) in both cell lines, although WEHI-231 cells are less susceptible than CH31. This effect was reversed by lipopolysaccharide, in agreement with the known effects of lipopolysaccharide on anti-Ig-induced growth inhibition. These results therefore indicate that these lymphomas afford a potentially interesting model to study the mechanisms of programmed cell death induced by ligation of the antigen receptors on normal B cells.
WEHI - 231和CH31是表型上未成熟的sIgM⁺小鼠B细胞淋巴瘤,其生长受到抗免疫球蛋白(Ig)抗体的抑制。因此,这些细胞系已被用作研究表面Ig受体在B细胞耐受性诱导中的作用的模型。我们在此表明,抗μ抗体在这两种细胞系中均诱导DNA裂解为程序性细胞死亡(凋亡)所特有的寡核小体片段,尽管WEHI - 231细胞比CH31细胞更不易感。脂多糖可逆转这种效应,这与脂多糖对抗Ig诱导的生长抑制的已知作用一致。因此,这些结果表明,这些淋巴瘤为研究正常B细胞上抗原受体的连接所诱导的程序性细胞死亡机制提供了一个潜在有趣的模型。