Lynes M A, Tibbetts D J, Swenson L M, Sidman C L
Department of Molecular and Cell Biology, University of Connecticut, Storrs 06269.
Cell Immunol. 1993 Oct 1;151(1):65-79. doi: 10.1006/cimm.1993.1222.
Spatial associations of individual plasma membrane components have been proposed as being important in the functional coupling of these molecules. CD45 and Thy-1 associate on the membranes of both transformed and normal lymphocytes as measured by several different methods, and both of these molecules have been found to contribute to T cell activation and proliferation. Thy-1, however, lacks both transmembrane and cytoplasmic domains (it is linked to the plasma membrane through a glucosyl-phosphatidylinositol linkage), obliging the activation and proliferation signals that act through Thy-1 to be transduced by neighboring molecules. In the experiments reported here, the association of Thy-1 and CD45 was examined on lymphocytes from two mutant mouse strains, C3H-gld/gld and C3H-lpr/lpr, both of which exhibit lymphocyte activation and proliferation parameters significantly different from the control C3H/HeJ strain. No significant differences in Thy-1/CD45 association (measured by a heterologous epitope blocking assay) to distinguish mutant from wild-type thymocytes were found. However, spatial associations of CD45 and Thy-1 were altered on both mutant lymph node cells and splenic lymphocytes. These abnormal associations suggested possible effects on the membrane protein tyrosine phosphatase (PTPase) activity associated with CD45. Both C3H-gld/gld and C3H-lpr/lpr lymph node cells were found to have significantly elevated levels of membrane PTPase activity, and this elevation correlated with the anergy to mitogens that develops as these animals age. Finally, monoclonal anti-Thy-1 antibody (G7) reduced the PTPase activity of wild-type membrane isolates, suggesting that Thy-1/PTPase interactions may be a mechanism by which G7 provokes a lymphoproliferative response.
单个质膜成分的空间关联被认为在这些分子的功能偶联中很重要。通过几种不同方法测量发现,CD45和Thy-1在转化和正常淋巴细胞的膜上相互关联,并且已发现这两种分子都有助于T细胞的活化和增殖。然而,Thy-1缺乏跨膜和细胞质结构域(它通过糖基磷脂酰肌醇连接与质膜相连),这使得通过Thy-1起作用的活化和增殖信号必须由相邻分子转导。在本文报道的实验中,研究了来自两种突变小鼠品系C3H-gld/gld和C3H-lpr/lpr的淋巴细胞上Thy-1与CD45的关联,这两种品系的淋巴细胞活化和增殖参数均与对照C3H/HeJ品系有显著差异。未发现Thy-1/CD45关联(通过异源表位阻断试验测量)在区分突变型和野生型胸腺细胞方面有显著差异。然而,CD45和Thy-1的空间关联在突变型淋巴结细胞和脾淋巴细胞上均发生了改变。这些异常关联提示可能对与CD45相关的膜蛋白酪氨酸磷酸酶(PTPase)活性有影响。发现C3H-gld/gld和C3H-lpr/lpr淋巴结细胞的膜PTPase活性水平均显著升高,并且这种升高与这些动物随着年龄增长而出现的对有丝分裂原的无反应性相关。最后,单克隆抗Thy-1抗体(G7)降低了野生型膜分离物的PTPase活性,提示Thy-1/PTPase相互作用可能是G7引发淋巴细胞增殖反应的一种机制。