cardiovascular system
N |
• no effect on development of aortic dissections or change in blood pressure
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Allele Symbol Allele Name Allele ID |
Best3tm1.1Zhoj targeted mutation 1.1, Jia-Guo Zhou MGI:7532855 |
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Summary |
2 genotypes
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
N |
• no effect on development of aortic dissections or change in blood pressure
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• treatment with angiotensin II to induce hypertension induced mortality in 32.3% of mice, similar treatment induced no deaths in controls
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• some die suddenly at 8 weeks of age
• gradual increase in mortality with age with 13 of 30 mice dying before 72 weeks of age
• treatment with ponatinib, which inhibits MEKK3 and MEKK2 signaling, increases survival rates
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• false lumen formation, intramural hematomas and dissections at 8 weeks of age
• media thickness, disorganization, and decreased expression of cyto-skeletal protein are seen before and after angiotensin II treatment
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• decreased thickness
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• disruption and degradation of collagen and medial elastic lamina
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• decreased medial thickness and degradation of the aortic wall
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• marked increase in diameter of the abdominal aorta at 8 weeks of age
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• marked increase in diameter at 8 weeks of age
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• incidence increases with age
• develop aortic hematoma or dissection at 8 weeks of age
• at 24 weeks of age, aortic rupture across the intima and media, dissection of the aortic wall with blood collection between the media and fragmentation the elastic layers are seen
• about 63% of mice receiving angiotensin II develop serious dissections in the aorta arch and abdominal aorta, dissections do not develop in similarly treated controls
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• dilated aneurysms in the thoracic and abdominal aorta from 24 weeks of age
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• from 24 weeks of age
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• from 24 weeks of age
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• mice die of massive hemorrhage in the thoracic or peritoneal cavity
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• increased apoptosis of vascular smooth muscle cells in the aorta
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• increased numbers of CD68-positive macrophages in the aorta indicating involvement of inflammation in the development of aortic dissection
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• increased numbers of CD68-positive macrophages in the aorta indicating involvement of inflammation in the development of aortic dissection
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• increased apoptosis of vascular smooth muscle cells in the aorta
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• increased apoptosis of vascular smooth muscle cells in the aorta
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Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
aortic dissection | DOID:0080685 | J:338981 |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 12/10/2024 MGI 6.24 |
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