Neurobiology Section, Division of Biological Sciences, University of California, San Diego, La Jolla, California 92093, USA; email:
Department of Neurosciences, School of Medicine, University of California, San Diego, La Jolla, California 92093, USA; email:
Annu Rev Cell Dev Biol. 2019 Oct 6;35:501-521. doi: 10.1146/annurev-cellbio-100617-062644.
The dual leucine zipper-bearing kinase (DLK) and leucine zipper-bearing kinase (LZK) are evolutionarily conserved MAPKKKs of the mixed-lineage kinase family. Acting upstream of stress-responsive JNK and p38 MAP kinases, DLK and LZK have emerged as central players in neuronal responses to a variety of acute and traumatic injuries. Recent studies also implicate their function in astrocytes, microglia, and other nonneuronal cells, reflecting their expanding roles in the multicellular response to injury and in disease. Of particular note is the potential link of these kinases to neurodegenerative diseases and cancer. It is thus critical to understand the physiological contexts under which these kinases are activated, as well as the signal transduction mechanisms that mediate specific functional outcomes. In this review we first provide a historical overview of the biochemical and functional dissection of these kinases. We then discuss recent findings on regulating their activity to enhance cellular protection following injury and in disease, focusing on but not limited to the nervous system.
双亮氨酸拉链激酶(DLK)和亮氨酸拉链激酶(LZK)是丝裂原活化蛋白激酶激酶家族中进化保守的 MAPKKK。作为应激反应性 JNK 和 p38 MAP 激酶的上游分子,DLK 和 LZK 已成为神经元对各种急性和创伤性损伤反应的核心分子。最近的研究还表明它们在星形胶质细胞、小胶质细胞和其他非神经元细胞中的功能,反映了它们在细胞对损伤的多细胞反应和疾病中的作用不断扩大。值得特别注意的是,这些激酶与神经退行性疾病和癌症之间存在潜在联系。因此,了解这些激酶被激活的生理环境以及介导特定功能结果的信号转导机制至关重要。在这篇综述中,我们首先提供了对这些激酶的生化和功能解析的历史概述。然后,我们讨论了最近关于调节它们的活性以增强损伤后和疾病中细胞保护的发现,重点但不限于神经系统。