Laboratory of Molecular Pharmacology, Biosignal Research Center, Kobe University, Kobe 657-8501, Japan.
Department of Agrobioscience, Graduate School of Agricultural Science, Kobe University, Kobe 657-8501, Japan.
Biochem Biophys Res Commun. 2014 Mar 7;445(2):340-5. doi: 10.1016/j.bbrc.2014.01.197. Epub 2014 Feb 7.
Diacylglycerol (DAG) is an important lipid that acts as a signaling messenger during mast cell degranulation after allergen cross-linking of immunoglobulin (Ig) E-bound FcεRI receptors. In this study, we determined the role of diacylglycerol kinase (DGK), which negatively regulates DAG-dependent signaling by converting DAG to phosphatidic acid (PA), in the regulation of mast cell degranulation. Treating RBL (rat basophilic leukemia)-2H3 mast cells with a type I DGK inhibitor significantly reduced antigen-induced degranulation and PA production. Among type I DGK isoforms, we observed that DGKα and DGKγ mRNAs were expressed in RBL-2H3 mast cells using reverse transcription polymerase chain reaction. DGKγ knockdown, but not DGKα, by isoform-specific short hairpin RNAs reduced mast cell degranulation and Ca(2+) influxes from the extracellular environment. These results suggest that DGKγ regulates mast cell degranulation after FcεRI cross-linking through mobilization of intracellular Ca(2+) through Ca(2+) influxes.
二酰基甘油 (DAG) 是一种重要的脂质,在过敏原交联 IgE 结合的 FcεRI 受体后,作为肥大细胞脱颗粒的信号信使发挥作用。在这项研究中,我们确定了二酰基甘油激酶 (DGK) 的作用,DGK 通过将 DAG 转化为磷酸脂酸 (PA) 来负调控 DAG 依赖性信号,从而调节肥大细胞脱颗粒。用 I 型 DGK 抑制剂处理 RBL(大鼠嗜碱性白血病)-2H3 肥大细胞可显著减少抗原诱导的脱颗粒和 PA 产生。在 I 型 DGK 同工型中,我们使用逆转录聚合酶链反应观察到 DGKα 和 DGKγ mRNA 在 RBL-2H3 肥大细胞中表达。用同工型特异性短发夹 RNA 敲低 DGKγ,但不是 DGKα,可减少肥大细胞脱颗粒和细胞外环境中 Ca(2+)的内流。这些结果表明,DGKγ 通过 Ca(2+)内流动员细胞内 Ca(2+),调节 FcεRI 交联后的肥大细胞脱颗粒。