Center for Molecular Medicine, China Medical University Hospital, Taichung, 40447, Taiwan.
J Biomed Sci. 2013 Jan 23;20(1):3. doi: 10.1186/1423-0127-20-3.
IκB kinase (IKK) complex, the master kinase for NF-κB activation, contains two kinase subunits, IKKα and IKKβ. In addition to mediating NF-κB signaling by phosphorylating IκB proteins during inflammatory and immune responses, the activation of the IKK complex also responds to various stimuli to regulate diverse functions independently of NF-κB. Although these two kinases share structural and biochemical similarities, different sub-cellular localization and phosphorylation targets between IKKα and IKKβ account for their distinct physiological and pathological roles. While IKKβ is predominantly cytoplasmic, IKKα has been found to shuttle between the cytoplasm and the nucleus. The nuclear-specific roles of IKKα have brought increasing complexity to its biological function. This review highlights major advances in the studies of the nuclear functions of IKKα and the mechanisms of IKKα nuclear translocation. Understanding the nuclear activity is essential for targeting IKKα for therapeutics.
IκB 激酶 (IKK) 复合物是 NF-κB 激活的主要激酶,包含两个激酶亚基,IKKα 和 IKKβ。在炎症和免疫反应过程中通过磷酸化 IκB 蛋白来介导 NF-κB 信号转导,IKK 复合物的激活还可以响应各种刺激,独立于 NF-κB 调节多种功能。尽管这两种激酶具有结构和生化相似性,但 IKKα 和 IKKβ 之间的亚细胞定位和磷酸化靶标不同,这解释了它们在生理和病理方面的不同作用。虽然 IKKβ 主要位于细胞质中,但已经发现 IKKα 在细胞质和细胞核之间穿梭。IKKα 的核特异性作用为其生物学功能带来了越来越多的复杂性。本文综述了 IKKα 的核功能及其核转位机制的研究进展。了解核活性对于靶向 IKKα 进行治疗至关重要。