Wanger L, Otteskog P, Sundqvist K G
Immunology. 1984 Jul;52(3):519-23.
When attached to a solid surface coated with protein A various antibodies reacting with lymphocyte membrane antigens (anti-beta 2m, OKT3, OKT8, Leu2, 3, 4 and certain patient sera) catalyse the formation of peripheral lamellar activity, i.e. an active spreading process in human T lymphocytes. In contrast, binding only of the same antibodies to the cells or allowing antibody-coated cells to settle and bind to a protein A-coated surface did not induce spreading although the number of cells attached to the solid surface was virtually the same as in the former case. The peripheral lamellar activity markedly facilitated short-range lymphocyte interactions and appeared to constitute the region of the lymphocyte that actively contacts other cells. These results show that antibodies can act as spreading factors, and indicate that this function is critically dependent on the presentation of the inducing ligand. The asymmetry in the induction of active cell edges may influence functional lymphocyte interactions with environmental surfaces.
当附着于涂有蛋白A的固体表面时,各种与淋巴细胞膜抗原发生反应的抗体(抗β2微球蛋白、OKT3、OKT8、Leu2、3、4以及某些患者血清)可催化外周板层活性的形成,即在人T淋巴细胞中发生的一种活跃铺展过程。相比之下,仅使相同抗体与细胞结合或让抗体包被的细胞沉降并结合到涂有蛋白A的表面上,并不会诱导铺展,尽管附着于固体表面的细胞数量实际上与前一种情况相同。外周板层活性显著促进了淋巴细胞的短程相互作用,并且似乎构成了淋巴细胞中与其他细胞进行主动接触的区域。这些结果表明,抗体可作为铺展因子,并且表明该功能严重依赖于诱导配体的呈递。活性细胞边缘诱导过程中的不对称性可能会影响淋巴细胞与周围环境表面的功能性相互作用。