Selection of membrane IgM- variants from a mIgM+ murine B lymphoma cell: problems and solutions.

R Andrews-Wagner, C H Sibley
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引用次数: 6

Abstract

We have used antibody-mediated complement killing to isolate membrane IgM-negative (mIgM-) variants from the mIgM+ murine B cell lymphoma, WEHI 279.1. This procedure has been used previously to select variants which lack expression of other cell-surface antigens on lymphoid cells. In those experiments, multiple rounds of selection have often been required for selection of the negative variants. We found that many cycles of selection produced very few variants and that those isolated had reduced, but still measurable, levels of mIgM. We were able to select large numbers of stable mIgM- variants by subjecting the populations with reduced levels of mIgM to two rounds of immunoselection within one cell cycle. These variants are stable and exhibit a variety of defects which are all expressed as a failure to display IgM on their external surface. Analysis of these variant clones at the biochemical level will begin to define the requirements for proper display of mIgM on the cell membrane of B lymphoma cells.

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从mIgM+小鼠B淋巴瘤细胞中选择膜IgM-变异:问题和解决方案。
我们使用抗体介导的补体杀伤从mIgM+小鼠B细胞淋巴瘤WEHI 279.1中分离出膜igm阴性(mIgM-)变体。这种方法以前被用来选择在淋巴样细胞上缺乏其他细胞表面抗原表达的变异。在这些实验中,通常需要多轮选择来选择负变体。我们发现,许多选择周期只产生很少的变异,而那些被分离的基因的mIgM水平降低了,但仍然是可测量的。通过在一个细胞周期内对mIgM水平降低的群体进行两轮免疫选择,我们能够选择大量稳定的mIgM-变体。这些变体是稳定的,并表现出各种缺陷,这些缺陷都表现为未能在其外表面显示IgM。在生化水平上对这些变异克隆的分析将开始确定在B淋巴瘤细胞的细胞膜上适当显示mIgM的要求。
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