Huang Zhihui, Wang Ying, Hu Guoqing, Zhou Jiliang, Mei Lin, Xiong Wen-Cheng
Department of Neuroscience and Regenerative Medicine and Department of Neurology.
Charlie Norwood VA Medical Center, Augusta, GA 30912, USA.
Cereb Cortex. 2016 May;26(5):2299-2310. doi: 10.1093/cercor/bhv292. Epub 2015 Dec 17.
Yes-associated protein (YAP) is a key transcriptional cofactor of the Hippo pathway, critical for the development of multiple organs. However, its role in the developing brain remains poorly understood. Here, we found that YAP was highly expressed in astrocytes and YAP deletion elevated the astrocytic activation in culture and in vivo, which was associated with microglial activation. At the molecular level, YAP in astrocytes was activated by IFNβ or ciliary neurotrophic factor (CNTF), which was necessary for IFNβ or CNTF induction of the suppressor of cytokine signaling 3 (SOCS3), a negative regulator of the Janus kinase-signal transducer and activator of transcription (JAK-STAT) inflammatory pathway. YAP(-/-) astrocytes thus showed hyperactivation of the JAK-STAT inflammatory pathway and reactive astrogliosis. Expression of SOCS3 in YAP(-/-) astrocytes prevented the hyperactivation of STAT3 and partially restored the astrocytic activation. Finally, reactive astrogliosis was associated with blood-brain barrier dysfunction in YAP brain-selective knockout mice. Taken together, these results identify unrecognized functions of YAP in preventing reactive astrogliosis and reveal a pathway of YAP-SOCS for the negatively control of neuroinflammation.
Yes相关蛋白(YAP)是Hippo信号通路的关键转录共激活因子,对多个器官的发育至关重要。然而,其在发育中的大脑中的作用仍知之甚少。在这里,我们发现YAP在星形胶质细胞中高表达,YAP缺失会在体外和体内升高星形胶质细胞的活化,这与小胶质细胞活化有关。在分子水平上,星形胶质细胞中的YAP被IFNβ或睫状神经营养因子(CNTF)激活,这是IFNβ或CNTF诱导细胞因子信号转导抑制因子3(SOCS3)所必需的,SOCS3是Janus激酶-信号转导子和转录激活子(JAK-STAT)炎症通路的负调节因子。因此,YAP(-/-)星形胶质细胞表现出JAK-STAT炎症通路的过度激活和反应性星形胶质细胞增生。SOCS3在YAP(-/-)星形胶质细胞中的表达可防止STAT3的过度激活,并部分恢复星形胶质细胞的活化。最后,反应性星形胶质细胞增生与YAP脑选择性敲除小鼠的血脑屏障功能障碍有关。综上所述,这些结果确定了YAP在预防反应性星形胶质细胞增生方面未被认识的功能,并揭示了一条YAP-SOCS负向控制神经炎症的途径。