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Merck

A connexin43/YAP axis regulates astroglial-mesenchymal transition in hemoglobin induced astrocyte activation.

Cell death and differentiation (2018-06-09)
Yong Yang, Jie Ren, Yuhao Sun, Yuan Xue, Zhijian Zhang, Aihua Gong, Baofeng Wang, Zhihong Zhong, Zhenwen Cui, Zhiyu Xi, Guo-Yuan Yang, Qingfang Sun, Liuguan Bian
RESUMEN

Reactive astrogliosis is a common response to insults to the central nervous system, but the mechanism remains unknown. In this study, we found the temporal and spatial differential expression of glial fibrillary acidic protein (GFAP) and Vimentin in the intracerebral hemorrhage (ICH) mouse brain, indicating that the de-differentiation and astroglial-mesenchymal transition (AMT) of astrocytes might be an early event in reactive astrogliosis. Further we verified the AMT finding in purified astrocyte cultures exposed to hemoglobin (Hb). Additionally, Connexin 43 (Cx43) downregulation and YAP nuclear translocation were observed in Hb-activated astrocytes. Knocking down Cx43 by siRNA triggered YAP nuclear translocation. Cx43 and YAP were physically associated as determined by immunofluorescence and co-immunoprecipitation. We propose that astrocytes undergo AMT during Hb-induced activation where Cx43 downregulation facilitates YAP nuclear translocation is a novel mechanism involved in this process. Cx43-YAP interaction may represent a potential therapeutic target for modulating astrocyte activation.

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Sigma-Aldrich
Anticuerpo anti-proteína gliofibrilar ácida, clon GA5, clone GA5, Chemicon®, from mouse
Sigma-Aldrich
Anticuerpo anti-vimentina, clon V9, clone V9, Chemicon®, from mouse
Sigma-Aldrich
Monoclonal Anti-Connexin-43 antibody produced in mouse, clone CXN-6, ascites fluid
Sigma-Aldrich
Anti-Connexin 43 antibody produced in rabbit, affinity isolated antibody