Journal article
Absence of glaucoma in DBA/2J mice homozygous for wild-type versions of Gpnmb and Tyrp1
BMC genetics, Vol.8(1), pp.45-45
2007
DOI: 10.1186/1471-2156-8-45
PMCID: PMC1937007
PMID: 17608931
Abstract
Background: The glaucomas are a common but incompletely understood group of diseases. DBA/2J mice develop a pigment liberating iris disease that ultimately causes elevated intraocular pressure (IOP) and glaucoma. We have shown previously that mutations in two genes, Gpnmb and Tyrp1, initiate the iris disease. However, mechanisms involved in the subsequent IOP elevation and optic nerve degeneration remain unclear.
Results: Here we present new mouse strains with Gpnmb and/or Tyrp1 genes of normal function and with a DBA/2J genetic background. These strains do not develop elevated IOP or glaucoma with age.
Conclusion: These strains provide much needed controls for studying pathogenic mechanisms of glaucoma using DBA/2J mice. Given the involvement of Gpnmb and/or Tyrp1 in areas such as immunology and tumor development and progression, these strains are also important in other research fields.
Details
- Title: Subtitle
- Absence of glaucoma in DBA/2J mice homozygous for wild-type versions of Gpnmb and Tyrp1
- Creators
- Gareth R Howell - The Jackson Laboratory, 600 Main Street, Bar Harbor, Maine, USARichard T Libby - The Jackson Laboratory, 600 Main Street, Bar Harbor, Maine, USAJeffrey K Marchant - Department of Anatomy and Cell Biology, Tufts University of Medicine, Boston, MA, USALawriston A Wilson - The Jackson Laboratory, 600 Main Street, Bar Harbor, Maine, USAIoan M Cosma - The Jackson Laboratory, 600 Main Street, Bar Harbor, Maine, USARichard S Smith - The Jackson Laboratory, 600 Main Street, Bar Harbor, Maine, USAMichael G Anderson - Department of Physiology and Biophysics, The University of Iowa, Iowa City, IA, USASimon WM John - The Jackson Laboratory, 600 Main Street, Bar Harbor, Maine, USA
- Resource Type
- Journal article
- Publication Details
- BMC genetics, Vol.8(1), pp.45-45
- Publisher
- BioMed Central; London
- DOI
- 10.1186/1471-2156-8-45
- PMID
- 17608931
- PMCID
- PMC1937007
- ISSN
- 1471-2156
- eISSN
- 1471-2156
- Language
- English
- Date published
- 2007
- Academic Unit
- Molecular Physiology and Biophysics; Ophthalmology and Visual Sciences
- Record Identifier
- 9984025594102771
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