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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Eno2-PTGS2)32Pasi
transgene insertion 32, Guilio Maria Pasinetti
MGI:3717604
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cx1
Tg(APP695)3Dbo/0
Tg(Eno2-PTGS2)32Pasi/0
Tg(PSEN1)5Dbo/0
involves: C3H/HeJ * C57BL/6J MGI:3720017
tg2
Tg(Eno2-PTGS2)32Pasi/0 involves: C3H/HeNTac * C57BL/6NTac MGI:3717606


Genotype
MGI:3720017
cx1
Allelic
Composition
Tg(APP695)3Dbo/0
Tg(Eno2-PTGS2)32Pasi/0
Tg(PSEN1)5Dbo/0
Genetic
Background
involves: C3H/HeJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(APP695)3Dbo mutation (3 available)
Tg(Eno2-PTGS2)32Pasi mutation (0 available)
Tg(PSEN1)5Dbo mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• no differences in neuron number in cingulate cortex relative to wild-type
• immunoreactive amyloid beta deposits are observed in the cingulate cortex in 12 month-old triple transgenic mice; deposits are most evident in gray matter of cingulare and enthorhinal cortex, and to lesser extent in non-neuronal layers of the hippocampal formation

homeostasis/metabolism
• immunoreactive amyloid beta deposits are observed in the cingulate cortex in 12 month-old triple transgenic mice; deposits are most evident in gray matter of cingulare and enthorhinal cortex, and to lesser extent in non-neuronal layers of the hippocampal formation




Genotype
MGI:3717606
tg2
Allelic
Composition
Tg(Eno2-PTGS2)32Pasi/0
Genetic
Background
involves: C3H/HeNTac * C57BL/6NTac
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• within 10 minutes of kainic acid infusion, vigorous status epilepticus leads to death in transgenic animals whereas no wild-type mice die after kainic acid treatment

behavior/neurological
• intensity of kainic acid-induced seizures is elevated in transgenic mice relative to wild-type
• severe seizures in kainic acid-treated mice are associated with generalized tonic-clonic seizures with wild seizure jumps, while wild-type mice do not show any myoclonic twitches

nervous system
N
• no amyloid beta deposits are observed in transgenic mouse brains
• no differences in neuron number in cingulate cortex relative to wild-type
• intensity of kainic acid-induced seizures is elevated in transgenic mice relative to wild-type
• severe seizures in kainic acid-treated mice are associated with generalized tonic-clonic seizures with wild seizure jumps, while wild-type mice do not show any myoclonic twitches
• PTGS2 overexpression in neurons potentiates amyloid beta-mediated neuronal apoptotic damage in cortico-hippocampal cultures
• in cultured cortico-hippocampal neurons, exposure to glutamate results in 46% impairment of redox activity compared to 31.2% in control neurons, indicating potentiation of excitotoxicity in vitro

homeostasis/metabolism
• in cultured cortico-hippocampal neurons, exposure to glutamate results in 46% impairment of redox activity compared to 31.2% in control neurons, indicating potentiation of excitotoxicity in vitro

cellular
• in cultured cortico-hippocampal neurons, exposure to glutamate results in 46% impairment of redox activity compared to 31.2% in control neurons, indicating potentiation of excitotoxicity in vitro





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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory