Kooyman D L, Byrne G W, Logan J S
Nextran, Princeton, N.J. 08540, USA.
Exp Nephrol. 1998 Mar-Apr;6(2):148-51. doi: 10.1159/000020516.
Recently, we and others demonstrated the unique potential for glycosyl phosphatidylinositol (GPI) anchored proteins to transfer from one cell membrane to another in a process we termed 'painting'. The GPI-anchored proteins were shown to transfer intact and functional. The full significance of this phenomenon has yet to be fully realized, but implications exist in many areas including disease transmission (prions), cell protection (endothelial cells), and senescence (erythrocytes). It is of interest to note that cells exhibiting limited or no biosynthetic capacity (spermatozoa and erythrocytes) have been implicated thus far in cell-cell transfer of GPI-linked molecules. This observation demonstrates the potential for GPI-linked proteins to be 'painted' onto cells which otherwise may be incapable of expressing exogenous proteins. We show in this paper that GPI-linked CD59 and decay-accelerating factor will transfer intact from erythrocytes to endothelial cells in transgenic mice. We also demonstrate that the transfer process occurs under physiological conditions using several experimental models including organ and bone marrow transplantation. We detail the procedure to effect transfer of GPI-linked proteins from one cell type to another in either an in vivo or in vitro system.
最近,我们和其他研究人员证明了糖基磷脂酰肌醇(GPI)锚定蛋白在一个我们称为“描绘”的过程中从一个细胞膜转移到另一个细胞膜的独特潜力。研究表明,GPI锚定蛋白在转移后保持完整且具有功能。这一现象的全部意义尚未完全明了,但在包括疾病传播(朊病毒)、细胞保护(内皮细胞)和衰老(红细胞)等许多领域都有潜在影响。值得注意的是,迄今为止,生物合成能力有限或无生物合成能力的细胞(精子和红细胞)已被牵涉到GPI连接分子的细胞间转移中。这一观察结果表明,GPI连接蛋白有可能被“描绘”到那些原本可能无法表达外源蛋白的细胞上。我们在本文中表明,在转基因小鼠中,GPI连接的CD59和衰变加速因子会从红细胞完整地转移到内皮细胞。我们还利用包括器官和骨髓移植在内的多种实验模型证明,这种转移过程发生在生理条件下。我们详细介绍了在体内或体外系统中实现GPI连接蛋白从一种细胞类型转移到另一种细胞类型的程序。