首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Adhesion-activating phorbol ester increases the mobility of leukocyte integrin LFA-1 in cultured lymphocytes.
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Adhesion-activating phorbol ester increases the mobility of leukocyte integrin LFA-1 in cultured lymphocytes.

机译:粘附激活佛波酯增加了白细胞整合素LFA-1在培养的淋巴细胞中的迁移率。

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摘要

Lymphocytes activate adhesion to intracellular adhesion mlecule 1 (ICAM-1) via leukocyte function associated antigen 1 (LFA-1), their major beta 2 integrin, in response to PMA (phorbol 12-myristate 13-acetate) without an increase in the number of receptors expressed. The molecular details of the mechanism are unknown. To determine the effect of PMA activation on LFA-1 movement within the plasma membrane, we used the single particle tracking technique to measure the diffusion rate of LFA-1 molecules on EBV-transformed B cells before and after PMA activation. Diffusion of LFA-1 on unactivated cells was restricted compared to CR1 (CD35), another transmembrane protein of equivalent size. PMA caused a 10-fold increase in the diffusion rate of LFA-1 without any effect on CD35. The increased LFA-1 motion induced by PMA was random, not directed, indicating that it was due to a release of constraints rather than the application of forces. The diffusion rates of LFA-1 are consistent with cytoskeletal attachment before and free diffusion after PMA. Cytochalasin D led to an equivalent increase in mobility and, at low doses, stimulated adhesion, implying that the nonadhesive state of LFA-1 is actively maintained by the lymphocyte cytoskeleton.
机译:淋巴细胞通过对白细胞功能相关抗原1(LFA-1)(主要的β2整联蛋白)的激活来激活对细胞内粘附分子1(ICAM-1)的粘附,而对PMA(佛波醇12-肉豆蔻酸酯13-乙酸酯)的反应却没有增加表达的受体。该机制的分子细节未知。为了确定PMA激活对LFA-1在质膜内运动的影响,我们使用了单粒子跟踪技术来测量LMA-1分子在PMA激活前后在EBV转化的B细胞上的扩散速率。与CR1(CD35)(另一种同等大小的跨膜蛋白)相比,LFA-1在未激活细胞上的扩散受到限制。 PMA导致LFA-1扩散速率增加10倍,而对CD35没有任何影响。由PMA引起的LFA-1运动的增加是随机的,不是定向的,这表明这是由于释放约束而不是施加力引起的。 LFA-1的扩散速率与PMA之前和之后的自由扩散相一致。细胞松弛素D导致同等的运动性增加,并且在低剂量时刺激粘附,这表明LFA-1的非粘附状态可通过淋巴细胞的细胞骨架积极维持。

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