Reagan Alaina, Gu Xiaowu, Hauck Stefanie M, Ash John D, Cao Guangwen, Thompson Timothy C, Elliott Michael H
Department of Ophthalmology, University of Oklahoma Health Sciences Center, 73104, Oklahoma City, OK, USA.
Oklahoma Center for Neuroscience, University of Oklahoma Health Sciences Center, 73104, Oklahoma City, OK, USA.
Adv Exp Med Biol. 2016;854:411-8. doi: 10.1007/978-3-319-17121-0_54.
Caveolin-1 (Cav-1), the scaffolding protein of caveolae, is expressed in several retinal cell types and is associated with ocular pathologies. Cav-1 modulates neuroinflammatory/neuroprotective responses to central nervous system injury. We have shown that loss of Cav-1 results in a blunted cytokine response in retinas challenged with inflammatory stimuli. As neuroinflammatory and neuroprotective signaling overlap in their cytokine production and downstream signaling pathways, we hypothesized that loss of Cav-1 may also suppress neuroprotective signaling in the retina. To test this, we subjected mice in which Cav-1 was deleted specifically in the retina to a neurodegenerative insult induced by sodium iodate (NaIO3) and measured STAT3 activation, a measure of neuroprotective signaling. Our results show that Cav-1 ablation blunts STAT3 activation induced by NaIO3. STAT3 activation in response to intravitreal administration of the IL-6 family cytokine, leukemia inhibitory factor (LIF), was not affected by Cav-1 deletion indicating a competent gp130 receptor response. Thus, Cav-1 modulates neuroprotective signaling by regulating the endogenous production of neuroprotective factors.
小窝蛋白-1(Cav-1)是小窝的支架蛋白,在几种视网膜细胞类型中表达,并与眼部疾病相关。Cav-1调节对中枢神经系统损伤的神经炎症/神经保护反应。我们已经表明,Cav-1的缺失导致在受到炎症刺激的视网膜中细胞因子反应减弱。由于神经炎症和神经保护信号在其细胞因子产生和下游信号通路中重叠,我们推测Cav-1的缺失也可能抑制视网膜中的神经保护信号。为了验证这一点,我们将视网膜中特异性缺失Cav-1的小鼠置于由碘酸钠(NaIO3)诱导的神经退行性损伤模型中,并测量STAT3激活情况,以此作为神经保护信号的指标。我们的结果表明,Cav-1基因敲除减弱了由NaIO3诱导的STAT3激活。玻璃体内注射IL-6家族细胞因子白血病抑制因子(LIF)后STAT3的激活不受Cav-1缺失的影响,表明gp130受体反应正常。因此,Cav-1通过调节神经保护因子的内源性产生来调节神经保护信号。