Articles by Cesar O. Romero in JoVE
في فيفو ديناميات الشبكية دبقية التنشيط خلال تنكس عصبي: متحد البؤر Ophthalmoscopic التصوير والقياس الشكلي خلية في الماوس الزرق Alejandra Bosco1, Cesar O. Romero1, Balamurali K. Ambati2, Monica L. Vetter1 1Department of Neurobiology & Anatomy, University of Utah, 2Department of Ophthalmology & Visual Sciences, University of Utah تنشيط الخلايا الدبقية الصغيرة وكثرة الدبيقيات استجابات الرئيسية لالتنكس العصبي المزمن. هنا، فإننا نقدم طرق لفي الجسم الحي، والتصور على المدى الطويل CX3CR1-GFP + الخلايا الدبقية الشبكية بواسطة تنظير العين متحد البؤر، وعتبة والمورفولوجية تحليل لتحديد وقياس تفعيلها. نحن نراقب التغيرات دبقية خلال المراحل المبكرة من الزرق المرتبطة بالتقدم في السن.
Other articles by Cesar O. Romero on PubMed
Early Reduction of Microglia Activation by Irradiation in a Model of Chronic Glaucoma PloS One. 2012 | Pubmed ID: 22952717 Glaucoma is a neurodegenerative disease that results in the progressive decline and ultimate death of retinal ganglion cells (RGCs). While multiple risk factors are associated with glaucoma, the mechanisms leading to onset and progression of the disease remain unknown. Molecular analysis in various glaucoma models has revealed involvement of non-neuronal cell populations, including astrocytes, Mueller glia and microglia, at early stages of glaucoma. High-dose irradiation was reported to have a significant long-term protective effect in the DBA/2J (D2) mouse model of glaucoma, although the cellular and molecular basis for this effect remains unclear. In particular, the acute effects of irradiation on specific cell populations, including non-neuronal cells, in the D2 retina and nerve have not been assessed. Here we report that irradiation induces transient reduction in proliferating microglia within the optic nerve head and glial lamina within the first week post-irradiation. This was accompanied by reduced microglial activation, with no effect on astrocyte gliosis in those regions. At later stages we confirm that early high-dose irradiation of the mouse head results in improvement of axonal structural integrity and anterograde transport function, without reduction of intraocular pressure. Thus reduced microglial activation induced by irradiation at early stages is associated with reduced optic nerve and retinal neurodegeneration in the D2 mouse model of glaucoma.
Neurodegeneration Severity is Anticipated by Early Microglia Alterations Monitored in Vivo in a Mouse Model of Chronic Glaucoma Disease Models & Mechanisms. Mar, 2015 | Pubmed ID: 25755083 Microglia serve key homeostatic roles, and respond to neuronal perturbation and decline with high spatiotemporal resolution. The course of all chronic CNS pathologies is thus paralleled by local microgliosis and microglia activation beginning at early stages. However, the possibility of using live monitoring of microglia during early disease progression to predict the severity of neurodegeneration has not been unexplored. Since the retina allows live tracking of fluorescent microglia in their intact niche, here we investigated their early changes in relation to later optic nerve neurodegeneration. Thus, we used the DBA/2J mouse model of inherited glaucoma, which develops progressive retinal ganglion cell degeneration of variable severity during aging, and thus represents a useful model to study pathogenic mechanisms of retinal ganglion cell decline similar to human glaucoma. We imaged CX3CR1(+/GFP) microglial cells in vivo at ages ranging from 1 to 5 months by confocal scanning laser ophthalmoscopy (cSLO) and quantified cell density and morphological activation. We detected early microgliosis at the optic nerve head (ONH), where axonopathy first manifests, and could track attenuation of this microgliosis induced by minocycline. We also observed heterogeneous and dynamic patterns of early microglia activation in the retina. When the same animals were aged and analyzed for the severity of optic nerve pathology at 10 months of age, we found a strong correlation with the levels of ONH microgliosis at 3 to 4 months. Our findings indicate that live imaging and monitoring the time course and levels of early retinal microgliosis and microglia activation in glaucoma could serve as indicators of future neurodegeneration severity.