Davidson W F, Morse H C, Sharrow S O, Chused T M
J Immunol. 1979 Mar;122(3):884-91.
Lymphoid cells from C57BL/6 mice homozygous for the me gene exhibit multiple phenotypic and functional abnormalities from early as one week of age. In the B cell population these include a reduction in the frequency of detectable surface Ig+ cells, alterations in the level of expression of surface IgM and IgD, an increase in the frequency of large cells, plasma cells and TNP-specific plaque forming cePS. Together these findings provide strong evidence for polyclonal activation of B cells. The high level of expression of xenotropic MuLV gp70 by me/me spleen and lymph node cells provides further evidence for lymphoid cell activation. In preliminary studies, me/me T cells appeared to be phenotypically and functionally less affected by the me gene. The distribution of Thy 1.2 on the surface of spleen and lymph node T cells varied from low to normal and the mitogenic responses to Con A and PHA were depressed. It remains to be determined what the basic deficiency in me/me mice is and whether it affects primarily B cells or all lymphoid cells.
对于me基因纯合的C57BL/6小鼠,其淋巴细胞从出生仅一周起就表现出多种表型和功能异常。在B细胞群体中,这些异常包括可检测到的表面Ig⁺细胞频率降低、表面IgM和IgD表达水平改变、大细胞、浆细胞和TNP特异性斑块形成细胞频率增加。这些发现共同为B细胞的多克隆激活提供了有力证据。me/me脾脏和淋巴结细胞中嗜异性MuLV gp70的高表达为淋巴细胞激活提供了进一步证据。在初步研究中,me/me T细胞在表型和功能上似乎受me基因的影响较小。脾脏和淋巴结T细胞表面Thy 1.2的分布从低到正常不等,对刀豆蛋白A和植物血凝素的促有丝分裂反应受到抑制。me/me小鼠的基本缺陷是什么,以及它是否主要影响B细胞或所有淋巴细胞,仍有待确定。