Department of Pathology and Laboratory Medicine, Perelman School of Medicine at the University of Pennsylvania Philadelphia, PA, USA.
Front Cell Dev Biol. 2016 Sep 7;4:96. doi: 10.3389/fcell.2016.00096. eCollection 2016.
The generation of diacylglycerol (DAG) is critical for promoting immune cell activation, regulation, and function. Diacylglycerol kinase ζ (DGKζ) serves as an important negative regulator of DAG by enzymatically converting DAG into phosphatidic acid (PA) to shut down DAG-mediated signaling. Consequently, the loss of DGKζ increases DAG levels and the duration of DAG-mediated signaling. However, while the enhancement of DAG signaling is thought to augment immune cell function, the loss of DGKζ can result in both immunoactivation and immunomodulation depending on the cell type and function. In this review, we discuss how different immune cell functions can be selectively modulated by DGKζ. Furthermore, we consider how targeting DGKζ can be potentially beneficial for the resolution of human diseases by either promoting immune responses important for protection against infection or cancer or dampening immune responses in immunopathologic conditions such as allergy and septic shock.
二酰基甘油(DAG)的产生对于促进免疫细胞的激活、调节和功能至关重要。二酰基甘油激酶 ζ(DGKζ)通过将 DAG 酶促转化为磷脂酸(PA)来关闭 DAG 介导的信号,从而作为 DAG 的重要负调节剂发挥作用。因此,DGKζ 的缺失会增加 DAG 水平和 DAG 介导的信号持续时间。然而,虽然增强 DAG 信号被认为可以增强免疫细胞功能,但 DGKζ 的缺失可能会导致免疫激活和免疫调节,具体取决于细胞类型和功能。在这篇综述中,我们讨论了 DGKζ 如何选择性地调节不同的免疫细胞功能。此外,我们还考虑了如何通过靶向 DGKζ 来促进对感染和癌症等保护至关重要的免疫反应,或在过敏和败血症休克等免疫病理条件下抑制免疫反应,从而有可能有益于人类疾病的解决。