首页> 外文期刊>Molecular biology of the cell >Continual production of phosphatidic acid by phospholipase D is essential for antigen-stimulated membrane ruffling in cultured mast cells
【24h】

Continual production of phosphatidic acid by phospholipase D is essential for antigen-stimulated membrane ruffling in cultured mast cells

机译:磷脂酶D连续产生磷脂酸对于培养的肥大细胞中抗原刺激的膜起皱至关重要

获取原文
获取原文并翻译 | 示例
           

摘要

Phospholipase Ds (PLDs) are regulated enzymes that generate phosphatidic acid (PA), a putative second messenger implicated in the regulation of vesicular trafficking and cytoskeletal reorganization. Mast cells, when stimulated with antigen, show a dramatic alteration in their cytoskeleton and also release their secretory granules by exocytosis. Butan-1-ol, which diverts the production of PA generated by PLD to the corresponding phosphatidylalcohol, was found to inhibit membrane ruffling when added together with antigen or when added after antigen. Inhibition by butan-1-ol was completely reversible because removal of butan-1-ol restored membrane ruffling. Measurements of PLD activation by antigen indicate a requirement for continual PA production during membrane ruffling, which was maintained for at least 30 min. PLD1 and PLD2 are both expressed in mast cells and green fluorescent protein-tagged proteins were used to identify PLD2 localizing to membrane ruffles of antigen-stimulated mast cells together with endogenous ADP ribosylation factor 6 (ARF6). In contrast, green fluorescent protein-PLD1 localized to intracellular vesicles and remained in this location after stimulation with antigen. Membrane ruffling was independent of exocytosis of secretory granules because phorbol 12-myristate 13-acetate increased membrane ruffling in the absence of exocytosis. Antigen or phorbol 12-myristate 13-acetate stimulation increased both PLD1 and PLD2 activity when expressed individually in RBL-2H3 cells. Although basal activity of PLD2-overexpressing cells is very high, membrane ruffling was still dependent on antigen stimulation. In permeabilized cells, antigen-stimulated phosphatidylinositol(4,5)bisphosphate synthesis was dependent on both ARF6 and PA generated from PLD. We conclude that both activation of ARF6 by antigen and a continual PLD2 activity are essential for local phosphatidylinositol(4,5)bisphosphate generation that regulates dynamic actin cytoskeletal rearrangements. [References: 52]
机译:磷脂酶Ds(PLDs)是受调节的酶,可产生磷脂酸(PA),这是推测的第二信使,与调节水泡运输和细胞骨架重组有关。肥大细胞受到抗原刺激后,其细胞骨架发生巨大变化,并通过胞吐作用释放出分泌性颗粒。当与抗原一起添加或在抗原之后添加时,发现将由PLD产生的PA的生产转移为相应的磷脂酰醇的Butan-1-ol可抑制膜起皱。 Butan-1-ol的抑制作用是完全可逆的,因为去除butan-1-ol可以恢复膜的波纹。抗原对PLD激活的测量表明,在膜起皱期间需要连续产生PA,并保持至少30分钟。 PLD1和PLD2均在肥大细胞中表达,绿色荧光蛋白标签蛋白与内源性ADP核糖基化因子6(ARF6)一起用于鉴定PLD2定位于抗原刺激的肥大细胞的膜纹。相反,绿色荧光蛋白-PLD1定位于细胞内囊泡,并在用抗原刺激后保留在该位置。膜起伏不依赖于分泌性颗粒的胞吐作用,因为在不存在胞吐作用的情况下,佛波12-肉豆蔻酸酯13-乙酸酯会增加膜起波纹。抗原或佛波醇12-肉豆蔻酸酯13-醋酸酯刺激在RBL-2H3细胞中单独表达时会增加PLD1和PLD2活性。尽管PLD2过表达细胞的基础活性很高,但膜起皱仍取决于抗原刺激。在透化的细胞中,抗​​原刺激的磷脂酰肌醇(4,5)双磷酸酯的合成依赖于从PLD产生的ARF6和PA。我们得出结论,通过抗原激活ARF6和持续的PLD2活性对于调节动态肌动蛋白细胞骨架重排的局部磷脂酰肌醇(4,5)双磷酸生成都是必不可少的。 [参考:52]

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