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Phenotypes Associated with This Genotype
Genotype
MGI:7564569
Allelic
Composition
Tnfaip2tm1.1Ohno/Tnfaip2tm1.1Ohno
Genetic
Background
C.Cg-Tnfaip2tm1.1Ohno
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tnfaip2tm1.1Ohno mutation (0 available); any Tnfaip2 mutation (32 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
renal/urinary system
• mice show a 2-fold increase in albuminuria at 6 weeks of age and an 8.5-fold increase at 24 weeks of age
• the number of CD44+ parietal epithelial cells (PECs) lying on the Bowmans capsule increase progressively with age
• podocyte injury (desmin staining and podocyte apoptosis) is seen as early as 6-10 weeks of age
• progressive reduction in podocin and synaptopodin expression and eventually in podocyte number
• focal glomerular sclerosis that worsens over time
• 18-week-old and 24-week-old mice show scarring involving 15% and about 25% of the glomeruli, respectively
• severity of scarring worsens progressively within individual glomeruli
• cuboidal CD44+ and Ki-67+ cells are seen in the tubules of older (18-week-old) mice
• however, macrophage infiltration and expression of CCL2 and TNF-alpha are unaltered within glomeruli and no IgM, C3, IgG, and IgA staining is seen indicating no inflammation
• cast formation is seen in tubules
• glomeruli show an early and progressive reduction in both mtDNA copy number and expression of mitochondrial transcription factor/genes
• glomeruli mitochondrial membrane potential undergoes progressive reduction and mitochondrial oxidative stress is enhanced
• however, glomeruli show normal mitochondrial structure and mitochondrial mass is not altered
• however, no changes in mitochondrial membrane potential and TFAM expression are seen in renal tubular epithelial cells
• cells positive for both the PEC marker annexin A3 and CD44 are seen in the glomerular tuft indicating activated PECs
• 6-week-old podocytes show increased apoptosis
• tunneling nanotube-mediated mitochondrial transfer is almost abolished in mutant podocytes
• study of mitochondrial bioenergetics shows that basal and maximal oxygen consumption rate, ATP-linked respiration, and reserve capacity are reduced in podocytes, most likely due to alterations in oxidative phosphorylation as nonmitochondrial respiration and proton leak are unaltered
• low reserve capacity indicates that mitochondria function at their maximal capacity and are unable to meet any additional ATP demand
• older mice exhibit a 40% reduction in creatinine clearance

homeostasis/metabolism
• mice show a 2-fold increase in albuminuria at 6 weeks of age and an 8.5-fold increase at 24 weeks of age
• mice show an early and progressive increase in N-acetyl-beta-D-glucosaminidase activity

cellular
• 6-week-old podocytes show increased apoptosis

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
focal segmental glomerulosclerosis DOID:1312 OMIM:PS603278
J:343202


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
08/02/2024
MGI 6.24
The Jackson Laboratory