mortality/aging
• 40% die or were euthanized due to poor health between 20-36 days of age
|
growth/size/body
• gain weight more slowly or stop gaining weight completely starting around 16 days of age, however food intake is normal
|
• onset of growth retardation is between 16 and 26 days of age
|
digestive/alimentary system
• crypt abscesses are prevalent in the ileum, colon, and rectum
|
• edematous colons
|
• anal mucus discharge
|
• intestinal inflammation progresses from distal to proximal bowel in most homozygotes
|
• inflammation is limited to the mucosa
• 11 of 12 have distal colon colitis as early as 11 days of age
• 3 of 12 showed proximal colon colitis at 11-14 days of age
• most 15 day or older homozygotes have both distal and proximal colon inflammation
|
• severe inflammation of the ileum, but not jejunum or stomach , with inflammation limited to the mucosa
|
homeostasis/metabolism
• edematous colons
|
• hypothermic under normal housing conditions and become even more hypothermic after being housed in metabolic cages (rest on grids without bedding for 24 hrs)
|
• higher levels of lipid hydroperoxide in the ileum and colon, but not jejunum
|
• myeloperoxidase activity is increased in colonic mucosa
|
endocrine/exocrine glands
• crypt abscesses are prevalent in the ileum, colon, and rectum
|
immune system
• intestinal inflammation progresses from distal to proximal bowel in most homozygotes
|
• inflammation is limited to the mucosa
• 11 of 12 have distal colon colitis as early as 11 days of age
• 3 of 12 showed proximal colon colitis at 11-14 days of age
• most 15 day or older homozygotes have both distal and proximal colon inflammation
|
• severe inflammation of the ileum, but not jejunum or stomach , with inflammation limited to the mucosa
|
Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
inflammatory bowel disease | DOID:0050589 |
OMIM:PS266600 |
J:71506 |