Xia Shuting, Zhou Zikai, Leung Celeste, Zhu Yuehua, Pan Xingxiu, Qi Junxia, Morena Maria, Hill Matthew N, Xie Wei, Jia Zhengping
The Key Laboratory of Developmental Genes and Human Disease, Jiangsu Co-innovation Center of Neuroregeneration, Southeast University, Nanjing, China.
Institute of Life Sciences, Collaborative Innovation Center for Brain Science, Southeast University, Nanjing, China.
Elife. 2016 Jun 14;5:e14653. doi: 10.7554/eLife.14653.
PAK1 inhibitors are known to markedly improve social and cognitive function in several animal models of brain disorders, including autism, but the underlying mechanisms remain elusive. We show here that disruption of PAK1 in mice suppresses inhibitory neurotransmission through an increase in tonic, but not phasic, secretion of endocannabinoids (eCB). Consistently, we found elevated levels of anandamide (AEA), but not 2-arachidonoylglycerol (2-AG) following PAK1 disruption. This increased tonic AEA signaling is mediated by reduced cyclooxygenase-2 (COX-2), and COX-2 inhibitors recapitulate the effect of PAK1 deletion on GABAergic transmission in a CB1 receptor-dependent manner. These results establish a novel signaling process whereby PAK1 upregulates COX-2, reduces AEA and restricts tonic eCB-mediated processes. Because PAK1 and eCB are both critically involved in many other organ systems in addition to the brain, our findings may provide a unified mechanism by which PAK1 regulates these systems and their dysfunctions including cancers, inflammations and allergies.
已知PAK1抑制剂能显著改善包括自闭症在内的多种脑部疾病动物模型的社交和认知功能,但其潜在机制仍不清楚。我们在此表明,小鼠中PAK1的缺失通过增加内源性大麻素(eCB)的持续性分泌而非阶段性分泌来抑制抑制性神经传递。一致地,我们发现PAK1缺失后花生四烯酸乙醇胺(AEA)水平升高,但2-花生四烯酸甘油酯(2-AG)水平未升高。这种持续性AEA信号的增加是由环氧化酶-2(COX-2)减少介导的,COX-2抑制剂以CB1受体依赖的方式重现了PAK1缺失对GABA能传递的影响。这些结果建立了一种新的信号传导过程,即PAK1上调COX-2,减少AEA并限制持续性eCB介导的过程。由于PAK1和eCB除了在大脑中之外还都关键地参与许多其他器官系统,我们的发现可能提供了一种统一的机制,通过该机制PAK1调节这些系统及其功能障碍,包括癌症、炎症和过敏。