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Phenotypes Associated with This Genotype
Genotype
MGI:2450095
Allelic
Composition
Pdgfbtm1Cbet/Pdgfbtm1Cbet
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pdgfbtm1Cbet mutation (0 available); any Pdgfb mutation (15 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Abnormal endothelial cell morphology and increased caveolae formation in Pdgfbtm1Cbet/Pdgfbtm1Cbet brains

mortality/aging
• ~25% of homozygotes die 1-2 days prior to birth (E17-E18.5) with a hemorrhagic and edematous phenotype
• ~75% of homozygotes die at birth

renal/urinary system
• at E17.5 or later, homozygotes exhibit a spotty kidney phenotype
• the mutant Bowman's capsule space contains blood-filled aneurysm-like structures
• at E17.5 or later, homozygotes exhibit abnormal mature glomerular bodies ("red spots") in the inner part of the cortex, with capillary aneurysms replacing the glomerular tufts
• at E17.5 or later, mutant glomeruli show absence or reduction of mesangial cells in the presence of a morphologically normal basement membrane
• at E17.5 or later, mutant glomeruli may show absence of mesangial cells
• at E17.5 or later, homozygotes exhibit smaller kidneys
• at E17.5 or later, homozygotes display empty urinary bladders, suggesting kidney dysfunction

cardiovascular system
• at E17.5 or later, homozygotes exhibit dilated thoracic large arteries as well as dilated mesenteric blood vessels (J:20017)
• however, no hypoplasia of smooth muscle cells is observed (J:20017)
• exhibit regional dilations along the blood vessel length that are not seen in wild-type (J:78912)
• exhibit a 2.5-fold increase in the number of caveolae in brain vessels (J:78912)
• at E17.5 or later, homozygotes display dilated thoracic large arteries
• at E16.5-E19, homozygotes display a dilated aorta with an extended, thinner aortic muscular wall
• at E16.5-E19, homozygotes display a dilated aorta with an extended, thinner aortic muscular wall
• endothelial cells in the brain exhibit a luminal surface that has multiple processes projecting into the lumen of the vessel
• thickness of endothelium varies considerably; in some areas the cytoplasm of the cells is very thin and in others it is thicker than in wild-type
• exhibit endothelial cell hyperplasia in the brain from E11.5 on, however hyperplasia is not seen in the perineural vascular plexus surrounding the brain
• exhibit increased capillary diameter in the brain
• the mutant Bowman's capsule space contains blood-filled aneurysm-like structures
• exhibit loss and altered organization of pericytes in placentas; pericytes are found in the labyrinthine layer but are reduced by about 50% and are completely absent from the spongiotrophoblast layer
• pericytes are displaced from multicellular core aggregates to scattered sites in the walls of dilated fetal vessels
• fetal vessels are dilated to a varying degree in placentas; seen by E13.5
• the fetal vessel parametric length and area is increased relative to the maternal lacunas in the labyrinthine layer at E17
• homozygotes dying at E17-E18.5 display dilated and congested subpericardial blood vessels
• at E17.5 or later, homozygotes exhibit enlarged and malformed hearts, with extreme dilation of all chambers and of the thoracic aortae
• homozygotes dying at E17-E18.5 show hypertrabeculated and thin-walled regions in the right ventricle
• at E19, most live embryos exhibit hemorrhages in subcutaneous regions, periscapular brown fat and the liver

hematopoietic system
• at E19, homozygotes display reduced hematocrits relative to wild-type mice
• at E19, homozygotes display reduced hemoglobin values relative to wild-type mice
• at E19, homozygotes exhibit a ~20% increase in MCV
• at E19, homozygotes show a ~85% reduction in thrombocyte counts relative to wild-type mice
• no differences in granulocyte, lymphocyte, and monocyte differential cell counts are observed

respiratory system
• all live homozygotes delivered by Cesarian section gasp for air a few times, then cease to breathe and die

liver/biliary system
• at E17.5 or later, homozygotes exhibit reduced liver volume

homeostasis/metabolism
• homozygotes dying at E17-E18.5 display a generalized subcutaneous edema

embryo
• fetal vessels are dilated to a varying degree in placentas; seen by E13.5
• the fetal vessel parametric length and area is increased relative to the maternal lacunas in the labyrinthine layer at E17
• nonendothelial labyrinthine cell number, dominated by the trophoblasts, is reduced by about 40%

nervous system
• many glia cells that are juxtaposed to the endothelial cells of vessels exhibit prominent swelling

muscle
• at E16.5-E19, homozygotes display a dilated aorta with an extended, thinner aortic muscular wall

integument
• homozygotes dying at E17-E18.5 display a generalized subcutaneous edema

growth/size/body
• at E17.5 or later, homozygotes exhibit enlarged and malformed hearts, with extreme dilation of all chambers and of the thoracic aortae

cellular
• at E17.5 or later, mutant glomeruli show absence or reduction of mesangial cells in the presence of a morphologically normal basement membrane
• at E17.5 or later, mutant glomeruli may show absence of mesangial cells


Contributing Projects:
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
05/21/2024
MGI 6.23
The Jackson Laboratory