Genetic context determines susceptibility to intraocular pressure elevation in a mouse pigmentary glaucoma-4

Copyright information:Taken from "Genetic context determines susceptibility to intraocular pressure elevation in a mouse pigmentary glaucoma"BMC Biology 2006;4():20-20.Published online 7 Jul 2006PMCID:PMC1543659.ns and the axoplasm only of diseased or dying axons. The majority of optic ner...

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Hauptverfasser: Anderson, Michael G, Libby, Richard T, Mao, Mao, Cosma, Ioan M, Wilson, Larry A, Smith, Richard S, John, Simon WM
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Libby, Richard T
Mao, Mao
Cosma, Ioan M
Wilson, Larry A
Smith, Richard S
John, Simon WM
description Copyright information:Taken from "Genetic context determines susceptibility to intraocular pressure elevation in a mouse pigmentary glaucoma"BMC Biology 2006;4():20-20.Published online 7 Jul 2006PMCID:PMC1543659.ns and the axoplasm only of diseased or dying axons. The majority of optic nerves had only the mild degree of damage that is typical for aged mice, as shown here in a comparison of optic nerves from: () typical 22-month-old B6, versus () typical 22-month-old B6.. This was true even in mice with the highest IOPs recorded in the study, as shown here with () 14-month-old B6.and () 22-month-old B6.. Scale bar = 10 μm. () The overall distribution of nerve damage was almost identical in both standard B6 and B6.mice. Although some mice of each genotype developed a "moderate" degree of damage with age, the degree of damage in these mice only just met inclusion criteria for the "moderate" level and never involved significant axon loss. It was, therefore, much milder in all of these "moderate" mice than is typical of "moderate" D2 mice [42, 43]. A single B6.nerve had severe damage. The similar damage distributions of both standard B6 and B6.mice indicates that the damage reflects age-related B6 changes that are not related to and glaucoma. For each group, the number of optic nerves graded for B6 and B6.were: (4–6 months) 10 and 8, (11–12 months) 19 and 22, (13–15 months) 29 and 38, (16–19 months) 28 and 28, (20–26 months) 24 and 17. (E) Quantitative axon counts (mean ± SEM) show no detectable axon loss in B6.compared with standard B6 mice. The similar damage distributions and lack of axon loss in both strains indicates that the detected damage reflects age-related B6 changes that are not related to and glaucoma. For each group, the number of randomly selected nerves utilized in quantitative axon counting for B6 and B6.were: (4- months) 6 and 6, (22–27 months) 8 and 10.
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The majority of optic nerves had only the mild degree of damage that is typical for aged mice, as shown here in a comparison of optic nerves from: () typical 22-month-old B6, versus () typical 22-month-old B6.. This was true even in mice with the highest IOPs recorded in the study, as shown here with () 14-month-old B6.and () 22-month-old B6.. Scale bar = 10 μm. () The overall distribution of nerve damage was almost identical in both standard B6 and B6.mice. Although some mice of each genotype developed a "moderate" degree of damage with age, the degree of damage in these mice only just met inclusion criteria for the "moderate" level and never involved significant axon loss. It was, therefore, much milder in all of these "moderate" mice than is typical of "moderate" D2 mice [42, 43]. A single B6.nerve had severe damage. The similar damage distributions of both standard B6 and B6.mice indicates that the damage reflects age-related B6 changes that are not related to and glaucoma. 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title Genetic context determines susceptibility to intraocular pressure elevation in a mouse pigmentary glaucoma-4
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