首页> 外文期刊>Current Opinion in Cell Biology >Avidity regulation of integrins: the driving force in leukocyte adhesion
【24h】

Avidity regulation of integrins: the driving force in leukocyte adhesion

机译:整联蛋白的亲和力调节:白细胞粘附的驱动力

获取原文
获取原文并翻译 | 示例
           

摘要

The activity of integrins on leukocytes is tightly controlled, and their adhesion capacity shifts rapidly when cells emigrate from the blood to the tissues. The leukocyte-specific #beta#2 integrin LFA-1 (#alpha#L#beta#2) is the most important integrin expressed by leukocytes that regulate lymphocyte migration and the initiation of an immune response through binding to ICAM-1, -2 or -3. The binding activity of LFA-1 is rapidly altered by intracellular stimuli that activate LFA-1. Although alterations in the affinity of LFA-1, which leads to enhanced ICAM-1 binding, have been proposed, evidence is emerging that dynamic reorganisation of LFA-1 into microclusters is the major mechanism that regulates its binding capacity.
机译:整联蛋白对白细胞的活性受到严格控制,并且当细胞从血液迁移到组织时,它们的粘附能力迅速改变。白细胞特异性#beta#2整联蛋白LFA-1(#alpha#L#beta#2)是白细胞表达的最重要的整联蛋白,它通过结合ICAM-1,-2调节淋巴细胞迁移和免疫应答的启动来调节淋巴细胞迁移或-3。 LFA-1的结合活性被激活LFA-1的细胞内刺激迅速改变。尽管已经提出了导致增强的ICAM-1结合的LFA-1亲和力的改变,但有证据表明,LFA-1向微团簇的动态重组是调节其结合能力的主要机制。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号