Phenotypes associated with this allele
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Glg1Gt(RST092)Byg mutation
(0 available);
any
Glg1 mutation
(64 available)
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mortality/aging
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• no homozygotes are obtained at E10.5-E15.5 or at weaning
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Glg1Gt(RST092)Byg mutation
(0 available);
any
Glg1 mutation
(64 available)
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immune system
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• at 4 days after i.p. thioglycollate injection, 10-wk-old heterozygotes exhibit significantly decreased intraperitoneal leukocytes relative to wild-type controls
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• following challenge with local TNF injection, 8-wk-old male heterozygotes show significantly decreased numbers of firmly attached leukocytes on endothelial cells in cremaster venules relative to wild-type controls
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• following challenge with local TNF injection, 8-wk-old male heterozygotes show increased numbers of rolling leukocytes in cremaster venules relative to wild-type controls
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hematopoietic system
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• at 4 days after i.p. thioglycollate injection, 10-wk-old heterozygotes exhibit significantly decreased intraperitoneal leukocytes relative to wild-type controls
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• following challenge with local TNF injection, 8-wk-old male heterozygotes show significantly decreased numbers of firmly attached leukocytes on endothelial cells in cremaster venules relative to wild-type controls
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• following challenge with local TNF injection, 8-wk-old male heterozygotes show increased numbers of rolling leukocytes in cremaster venules relative to wild-type controls
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cellular
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• at 4 days after i.p. thioglycollate injection, 10-wk-old heterozygotes exhibit significantly decreased intraperitoneal leukocytes relative to wild-type controls
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• following challenge with local TNF injection, 8-wk-old male heterozygotes show significantly decreased numbers of firmly attached leukocytes on endothelial cells in cremaster venules relative to wild-type controls
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• following challenge with local TNF injection, 8-wk-old male heterozygotes show increased numbers of rolling leukocytes in cremaster venules relative to wild-type controls
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cardiovascular system
N |
• heterozygotes are viable and develop normally with no apparent phenotypic abnormalities in the unchallenged state
• at 18 weeks of age, heterozygotes fed a high-fat, high-sucrose diet for 10 weeks display an impaired endothelial-dependent relaxation response to acetylcholine, that is similar in extent to that seen in wild-type controls
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Apoetm1Unc mutation
(33 available);
any
Apoe mutation
(146 available)
Glg1Gt(RST092)Byg mutation
(0 available);
any
Glg1 mutation
(64 available)
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cardiovascular system
N |
• mice exhibit no significant differences in right and left ventricular chamber thickness or in myocardial collagen deposition relative to Apoetm1Unc homozygotes
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• after 9 weeks on a Western diet, mice exhibit atherosclerotic lesions with increased collagen deposition and fewer macrophages per mm2 of lesion relative to lesions from Apoetm1Unc homozygotes, as shown by collagen-specific (Sirius Red) and macrophage-specific (CD68) staining of aortic valves
• altered lesion composition suggests increased plaque stability; however, no differences in lesion area and thickness or in accumulation of smooth muscle cells are observed relative to Apoetm1Unc homozygotes
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immune system
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• after 9 weeks on a Western diet, mice exhibit a significantly reduced macrophage content in atherosclerotic lesions relative to Apoetm1Unc homozygotes
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• mice exhibit a significantly reduced macrophage content and CD68 expression in liver tissue relative to Apoetm1Unc homozygotes
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hematopoietic system
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• after 9 weeks on a Western diet, mice exhibit a significantly reduced macrophage content in atherosclerotic lesions relative to Apoetm1Unc homozygotes
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• mice exhibit a significantly reduced macrophage content and CD68 expression in liver tissue relative to Apoetm1Unc homozygotes
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homeostasis/metabolism
cellular
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• after 9 weeks on a Western diet, mice exhibit a significantly reduced macrophage content in atherosclerotic lesions relative to Apoetm1Unc homozygotes
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