Differential response of C57BL/6J mouse and DBA/2J mouse to optic nerve crush

<p>Abstract</p> <p>Background</p> <p>Retinal ganglion cell (RGC) death is the final consequence of many blinding diseases, where there is considerable variation in the time course and severity of RGC loss. Indeed, this process appears to be influenced by a wide variety...

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Main Authors: Williams Robert W, Orr William E, Freeman-Anderson Natalie E, Vazquez-Chona Felix, Nassr Mohamed, Templeton Justin P, Geisert Eldon E
Format: Article
Language:English
Published: BMC 2009-07-01
Series:BMC Neuroscience
Online Access:http://www.biomedcentral.com/1471-2202/10/90
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author Williams Robert W
Orr William E
Freeman-Anderson Natalie E
Vazquez-Chona Felix
Nassr Mohamed
Templeton Justin P
Geisert Eldon E
author_facet Williams Robert W
Orr William E
Freeman-Anderson Natalie E
Vazquez-Chona Felix
Nassr Mohamed
Templeton Justin P
Geisert Eldon E
author_sort Williams Robert W
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>Retinal ganglion cell (RGC) death is the final consequence of many blinding diseases, where there is considerable variation in the time course and severity of RGC loss. Indeed, this process appears to be influenced by a wide variety of genetic and environmental factors. In this study we explored the genetic basis for differences in ganglion cell death in two inbred strains of mice.</p> <p>Results</p> <p>We found that RGCs are more susceptible to death following optic nerve crush in C57BL/6J mice (54% survival) than in DBA/2J mice (62% survival). Using the Illumina Mouse-6 microarray, we identified 1,580 genes with significant change in expression following optic nerve crush in these two strains of mice. Our analysis of the changes occurring after optic nerve crush demonstrated that the greatest amount of change (44% of the variance) was due to the injury itself. This included changes associated with ganglion cell death, reactive gliosis, and abortive regeneration. The second pattern of gene changes (23% of the variance) was primarily related to differences in gene expressions observed between the C57BL/6J and DBA/2J mouse strains. The remaining changes in gene expression represent interactions between the effects of optic nerve crush and the genetic background of the mouse. We extracted one genetic network from this dataset that appears to be related to tissue remodeling. One of the most intriguing sets of changes included members of the crystallin family of genes, which may represent a signature of pathways modulating the susceptibility of cells to death.</p> <p>Conclusion</p> <p>Differential responses to optic nerve crush between two widely used strains of mice were used to define molecular networks associated with ganglion cell death and reactive gliosis. These results form the basis for our continuing interest in the modifiers of retinal injury.</p>
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spelling doaj.art-b951900c2f244d40897dd6b3c9b2795a2022-12-22T02:49:10ZengBMCBMC Neuroscience1471-22022009-07-011019010.1186/1471-2202-10-90Differential response of C57BL/6J mouse and DBA/2J mouse to optic nerve crushWilliams Robert WOrr William EFreeman-Anderson Natalie EVazquez-Chona FelixNassr MohamedTempleton Justin PGeisert Eldon E<p>Abstract</p> <p>Background</p> <p>Retinal ganglion cell (RGC) death is the final consequence of many blinding diseases, where there is considerable variation in the time course and severity of RGC loss. Indeed, this process appears to be influenced by a wide variety of genetic and environmental factors. In this study we explored the genetic basis for differences in ganglion cell death in two inbred strains of mice.</p> <p>Results</p> <p>We found that RGCs are more susceptible to death following optic nerve crush in C57BL/6J mice (54% survival) than in DBA/2J mice (62% survival). Using the Illumina Mouse-6 microarray, we identified 1,580 genes with significant change in expression following optic nerve crush in these two strains of mice. Our analysis of the changes occurring after optic nerve crush demonstrated that the greatest amount of change (44% of the variance) was due to the injury itself. This included changes associated with ganglion cell death, reactive gliosis, and abortive regeneration. The second pattern of gene changes (23% of the variance) was primarily related to differences in gene expressions observed between the C57BL/6J and DBA/2J mouse strains. The remaining changes in gene expression represent interactions between the effects of optic nerve crush and the genetic background of the mouse. We extracted one genetic network from this dataset that appears to be related to tissue remodeling. One of the most intriguing sets of changes included members of the crystallin family of genes, which may represent a signature of pathways modulating the susceptibility of cells to death.</p> <p>Conclusion</p> <p>Differential responses to optic nerve crush between two widely used strains of mice were used to define molecular networks associated with ganglion cell death and reactive gliosis. These results form the basis for our continuing interest in the modifiers of retinal injury.</p>http://www.biomedcentral.com/1471-2202/10/90
spellingShingle Williams Robert W
Orr William E
Freeman-Anderson Natalie E
Vazquez-Chona Felix
Nassr Mohamed
Templeton Justin P
Geisert Eldon E
Differential response of C57BL/6J mouse and DBA/2J mouse to optic nerve crush
BMC Neuroscience
title Differential response of C57BL/6J mouse and DBA/2J mouse to optic nerve crush
title_full Differential response of C57BL/6J mouse and DBA/2J mouse to optic nerve crush
title_fullStr Differential response of C57BL/6J mouse and DBA/2J mouse to optic nerve crush
title_full_unstemmed Differential response of C57BL/6J mouse and DBA/2J mouse to optic nerve crush
title_short Differential response of C57BL/6J mouse and DBA/2J mouse to optic nerve crush
title_sort differential response of c57bl 6j mouse and dba 2j mouse to optic nerve crush
url http://www.biomedcentral.com/1471-2202/10/90
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