Literature DB >> 16505037

Complement component 1Q (C1Q) upregulation in retina of murine, primate, and human glaucomatous eyes.

Kalliopi Stasi1, Dalia Nagel, Xiaoyan Yang, Rong-Fang Wang, Lizhen Ren, Steven M Podos, Thom Mittag, John Danias.   

Abstract

PURPOSE: Complement has been implicated in the pathogenesis of neurodegenerative diseases. The purpose of this study was to investigate whether complement activation is part of the pathogenesis of retinal ganglion cell (RGC) loss in glaucoma.
METHODS: mRNA and protein was extracted from the retina and brain of DBA/2 and C57/BL6 mice and subjected to RT-PCR and immunoblot analysis, respectively. In addition, eyes from the same mouse strains were subjected to immunohistochemistry with antibodies specific to complement component 1q (C1q). Eyes from monkeys with unilateral experimental glaucoma were also subjected to immunohistochemical analysis, as were eyes from human subjects with or without glaucoma.
RESULTS: C1q mRNA and C1q protein were found to be upregulated in the retina of glaucomatous DBA/2 mice. Upregulation of C1q preceded the time of extensive RGC death and increased with increasing age to 15 months in the retina, but not in the brain. No age-related C1q upregulation was detected in the reference mouse strain (C57BL/6), which develops significant nonglaucomatous RGC loss toward the end of the same time frame. C1q upregulation was also detected in laser-induced glaucomatous monkey eyes and in some (but not all) eyes of patients with glaucoma. C1q upregulation was localized to the Müller cells within the retina and in the area of the inner limiting membrane.
CONCLUSIONS: Complement expression is upregulated in the retina of two commonly used glaucoma models (in the DBA/2 mouse and the monkey) and in some human glaucomatous eyes. The timing of this upregulation suggests that complement activation plays a significant role in the pathogenesis of glaucoma.

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Year:  2006        PMID: 16505037     DOI: 10.1167/iovs.05-0830

Source DB:  PubMed          Journal:  Invest Ophthalmol Vis Sci        ISSN: 0146-0404            Impact factor:   4.799


  85 in total

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2.  Complement C3-Targeted Gene Therapy Restricts Onset and Progression of Neurodegeneration in Chronic Mouse Glaucoma.

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3.  Retinal cell responses to elevated intraocular pressure: a gene array comparison between the whole retina and retinal ganglion cell layer.

Authors:  Ying Guo; William O Cepurna; Jennifer A Dyck; Tom A Doser; Elaine C Johnson; John C Morrison
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4.  Retinal gene expression changes related to IOP exposure and axonal loss in DBA/2J mice.

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Review 5.  Differential gene expression in glaucoma.

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Review 7.  The pivotal role of the complement system in aging and age-related macular degeneration: hypothesis re-visited.

Authors:  Don H Anderson; Monte J Radeke; Natasha B Gallo; Ethan A Chapin; Patrick T Johnson; Christy R Curletti; Lisa S Hancox; Jane Hu; Jessica N Ebright; Goldis Malek; Michael A Hauser; Catherine Bowes Rickman; Dean Bok; Gregory S Hageman; Lincoln V Johnson
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8.  Network analysis of human glaucomatous optic nerve head astrocytes.

Authors:  Tatiana Nikolskaya; Yuri Nikolsky; Tatiana Serebryiskaya; Svetlana Zvereva; Eugene Sviridov; Zoltan Dezso; Eugene Rahkmatulin; Richard J Brennan; Nick Yankovsky; Sanjoy K Bhattacharya; Olga Agapova; M Rosario Hernandez; Valery I Shestopalov
Journal:  BMC Med Genomics       Date:  2009-05-09       Impact factor: 3.063

9.  Differential gene expression in mouse retina related to regional differences in vulnerability to hyperoxia.

Authors:  Yuan Zhu; Riccardo Natoli; Krisztina Valter; Jonathan Stone
Journal:  Mol Vis       Date:  2010-04-28       Impact factor: 2.367

10.  Early Involvement of Immune/Inflammatory Response Genes in Retinal Degeneration in DBA/2J Mice.

Authors:  W Fan; X Li; W Wang; J S Mo; H Kaplan; N G F Cooper
Journal:  Ophthalmol Eye Dis       Date:  2010-03-11
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