mortality/aging
• mice die around 17 months of age
|
renal/urinary system
• proliferation of kidney cells is increased compared to in wild-type mice
|
kidney cyst
(
J:157952
)
• at 1 month of age, mice exhibit scattered tubular microcysts unlike wild-type mice
• at 9 months, mice develop cysts unlike wild-type mice
• by 12 to 16 months, mice exhibit severe cysts unlike wild-type mice
• mice develop cysts in the medulla, cortex and glomeruli unlike wild-type mice
• mice develop hemorrhagic cysts unlike wild-type mice
• cysts exhibit proteinaceous casts in tubular cysts and interstitial fibrosis unlike wild-type mice
• cysts originate from the proximal and collecting ducts and glomeruli unlike in wild-type mice
• cysts exhibit calcium deposits
|
• bilateral
|
• at 15 months, urine creatinine content is reduced compared to in wild-type mice
|
• at 15 months
|
• at 4 months, mice exhibit non-selective proteinuria unlike wild-type mice
|
• at 15 months, urine nitrogen content is reduced compared to in wild-type mice
|
• partial and total
|
• cystic and non-cystic tubules exhibit epithelial hyperplasia and hypertrophy with occasional polyps of varying severity unlike wild-type mice
|
• at 1 month of age
|
• at 7 to 16 months
|
• at 1 month, mice exhibit mild tubular dilation unlike wild-type mice
• at 7 months mice develop glomerular and tubular dilation unlike wild-type mice
|
renal cast
(
J:157952
)
• proteinaceous casts in tubular cysts
|
• calcium deposits were limited to the renal papilla
|
pale kidney
(
J:157952
)
cardiovascular system
• thickness is increased
|
• mice exhibit evidence of eccentric dilated cardiac hypertrophy
|
• left ventricular wall systolic and diastolic thickness are increased compared to in wild-type mice indicating hypertrophy
|
• aortic valve leaflets are opaque rather than translucent as in wild-type mice
|
• left ventricular wall systolic and diastolic thickness are increased compared to in wild-type mice indicating hypertrophy
|
• aortic root diameter and area are increased compared to in wild-type mice
|
• mice exhibit increased fractional ejection and shortening compared with wild-type mice
|
liver/biliary system
liver cyst
(
J:157952
)
• in 1 in 32 mice, likely of cholangiocye origins, and affecting preferentially female mice
|
• mice exhibit broad band fibrosis along intrahepatic ducts unlike wild-type mice
• hepatic fibrosis is 4- to 5-fold greater than in wild-type mice
|
hematopoietic system
• at 15 months
|
homeostasis/metabolism
• at 15 months, urine creatinine content is reduced compared to in wild-type mice
|
• at 15 months
|
• at 15 months
|
• at 15 months
|
• at 4 months, mice exhibit non-selective proteinuria unlike wild-type mice
|
• at 15 months, urine nitrogen content is reduced compared to in wild-type mice
|
muscle
• left ventricular wall systolic and diastolic thickness are increased compared to in wild-type mice indicating hypertrophy
|
• mice exhibit increased fractional ejection and shortening compared with wild-type mice
|
cellular
• proliferation of kidney cells is increased compared to in wild-type mice
|
growth/size/body
• mice exhibit evidence of eccentric dilated cardiac hypertrophy
|
• left ventricular wall systolic and diastolic thickness are increased compared to in wild-type mice indicating hypertrophy
|
kidney cyst
(
J:157952
)
• at 1 month of age, mice exhibit scattered tubular microcysts unlike wild-type mice
• at 9 months, mice develop cysts unlike wild-type mice
• by 12 to 16 months, mice exhibit severe cysts unlike wild-type mice
• mice develop cysts in the medulla, cortex and glomeruli unlike wild-type mice
• mice develop hemorrhagic cysts unlike wild-type mice
• cysts exhibit proteinaceous casts in tubular cysts and interstitial fibrosis unlike wild-type mice
• cysts originate from the proximal and collecting ducts and glomeruli unlike in wild-type mice
• cysts exhibit calcium deposits
|
• bilateral
|
liver cyst
(
J:157952
)
• in 1 in 32 mice, likely of cholangiocye origins, and affecting preferentially female mice
|