Biochemical and biophysical research communications · 2018
Inhibition of TBK1 reduces choroidal neovascularization in vitro and in vivo.
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Cui Kaixuan, Zhang Shanshan, Liu Xiaojuan, Yan Zhenzhen, Huang Lili, Yang Xiaowei, Zhu Rongrong, Sang Aimin
Аннотация
choroidal neovascularization (CNV), a characteristic of wet age-related macular degeneration (AMD), causes severe vision loss among elderly patients. TANK-binding kinase 1 (TBK1) is a ubiquitously expressed serine-threonine kinase and is found to induce endothelial cells proliferation, represent a novel mediator of tumor angiogenesis and exert pro-inflammatory effect. However, the role of TBK1 in choroidal neovascularization has not been investigated so far. In this study, we found that the expression of TBK1 and VEGF was up-regulated in RF/6 A cells chemical hypoxia model and laser-induced mouse CNV model. Silencing of TBK1 suppressed the proliferation and tube formation activity of RF/6 A cells. Intravitreal injection of anti-TBK1 monoclonal antibody ameliorates CNV formation. Taken together, these findings exhibit a proangiogenic role for TBK1 via upregulating the expression of VEGF, and may suggest that TBK1 inhibition offers a unique and alternative method for prevention and treatment of AMD.
Предметные рубрики MeSH
AgedAnimalsAntibodies, MonoclonalCell HypoxiaCell LineChoroidal NeovascularizationDisease Models, AnimalGene Knockdown TechniquesHumansMacular DegenerationMiceMice, Inbred C57BLProtein Serine-Threonine KinasesRNA, Small InterferingRetinal Pigment EpitheliumUp-RegulationVascular Endothelial Growth Factor A