Stupack D G, Shen C, Wilkins J A
Rheumatic Disease Unit Research Laboratory, University of Manitoba, Winnipeg, Canada.
Cell Immunol. 1994 Apr 15;155(1):237-45. doi: 10.1006/cimm.1994.1116.
The control of lymphocyte adhesion is critical for proper cellular functions. The alpha 2 beta 1 integrin complex serves as a receptor for collagen on lymphocytes. The T cell leukemia Jurkat expresses alpha 2 beta 1 in a latent form on the cell surface. Three types of stimuli, antibody to the alpha 2 chain (JBS2), antibody to the beta 1 chain (JB1B), and phorbol ester (PMA), each induce activation of alpha 2 beta 1-dependent Jurkat binding to collagen. A comparison of the JBS2, JB1B, and PMA induction requirements indicated that the JB1B and the JBS2 effects are not sensitive to staurosporine while the PMA response is completely inhibited. Combinations of functionally saturating concentrations of the stimuli displayed an additive effect. Collectively these results suggest that several factors contribute to the generation of full integrin functionality and cellular adhesion, thus providing a possible basis for incrementally controlling the adhesive potential of lymphoid cells.
淋巴细胞黏附的控制对于正常细胞功能至关重要。α2β1整合素复合体作为淋巴细胞上胶原蛋白的受体。T细胞白血病Jurkat细胞在细胞表面以潜伏形式表达α2β1。三种类型的刺激,即α2链抗体(JBS2)、β1链抗体(JB1B)和佛波酯(PMA),每种都能诱导α2β1依赖的Jurkat细胞与胶原蛋白结合的激活。对JBS2、JB1B和PMA诱导条件的比较表明,JB1B和JBS2的作用对星形孢菌素不敏感,而PMA反应则被完全抑制。功能饱和浓度的刺激组合显示出相加效应。总体而言,这些结果表明,有几个因素有助于产生完整的整合素功能和细胞黏附,从而为逐步控制淋巴细胞的黏附潜能提供了可能的基础。