Literature DB >> 25740847

Mutated myocilin and heterozygous Sod2 deficiency act synergistically in a mouse model of open-angle glaucoma.

Myung Kuk Joe1, Naoki Nakaya1, Mones Abu-Asab2, Stanislav I Tomarev3.   

Abstract

Glaucoma is a multifactorial optic neuropathy characterized by retinal ganglion cell (RGC) death and axonal degeneration leading to irreversible blindness. Mutations in the myocilin (MYOC) gene are the most common genetic factors of primary open-angle glaucoma. To develop a genetic mouse model induced by the synergistic interaction of mutated myocilin and another significant risk factor, oxidative stress, we produced double-mutant mice (Tg-MYOC(Y437H/+)/Sod2(+/-)) bearing human MYOC with a Y437H point mutation and a heterozygous deletion of the gene for the primary antioxidant enzyme, superoxide dismutase 2 (SOD2). Sod2 is broadly expressed in most tissues including the trabecular meshwork (TM) and heterozygous Sod2 knockout mice exhibit the reduced SOD2 activity and oxidative stress in all studied tissues. Accumulation of Y437H myocilin in the TM induced endoplasmic reticulum stress and led to a 45% loss of smooth muscle alpha-actin positive cells in the eye drainage structure of 10- to 12-month-old Tg-MYOC(Y437H/+)/Sod2(+/-) mice as compared with wild-type littermates. Tg-MYOC(Y437H/+)/Sod2(+/-) mice had higher intraocular pressure, lost about 37% of RGCs in the peripheral retina, and exhibited axonal degeneration in the retina and optic nerve as compared with their wild-type littermates. Single-mutant littermates containing MYOC(Y437H/+) or Sod2(+/-) exhibited no significant pathological changes until 12 months of age. Additionally, we observed elevated expression of endothelial leukocyte adhesion molecule-1, a human glaucoma marker, in the TM of Tg-MYOC(Y437H/+)/Sod2(+/-) mice. This is the first reported animal glaucoma model that combines expression of a glaucoma-causing mutant gene and an additional mutation mimicking a deleterious environment factor that acts synergistically. Published by Oxford University Press 2015. This work is written by (a) US Government employee(s) and is in the public domain in the US.

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Year:  2015        PMID: 25740847      PMCID: PMC4447889          DOI: 10.1093/hmg/ddv082

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  74 in total

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3.  Analysis of myocilin mutations in 1703 glaucoma patients from five different populations.

Authors:  J H Fingert; E Héon; J M Liebmann; T Yamamoto; J E Craig; J Rait; K Kawase; S T Hoh; Y M Buys; J Dickinson; R R Hockey; D Williams-Lyn; G Trope; Y Kitazawa; R Ritch; D A Mackey; W L Alward; V C Sheffield; E M Stone
Journal:  Hum Mol Genet       Date:  1999-05       Impact factor: 6.150

Review 4.  Oxidative stress in glaucomatous neurodegeneration: mechanisms and consequences.

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Review 3.  Common and rare myocilin variants: Predicting glaucoma pathogenicity based on genetics, clinical, and laboratory misfolding data.

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4.  Myocilin Regulates Metalloprotease 2 Activity Through Interaction With TIMP3.

Authors:  Myung Kuk Joe; Raquel L Lieberman; Naoki Nakaya; Stanislav I Tomarev
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5.  Transgenic Overexpression of Myocilin Leads to Variable Ocular Anterior Segment and Retinal Alterations Associated with Extracellular Matrix Abnormalities in Adult Zebrafish.

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6.  Structure‒function‒pathogenicity analysis of C-terminal myocilin missense variants based on experiments and 3D models.

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Review 7.  Physiological function of myocilin and its role in the pathogenesis of glaucoma in the trabecular meshwork (Review).

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