About   Help   FAQ
Phenotypes Associated with This Genotype
Genotype
MGI:2653297
Allelic
Composition
Cd5ltm1Nto/Cd5ltm1Nto
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cd5ltm1Nto mutation (0 available); any Cd5l mutation (28 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• the CD4/CD8 double-positive (DP) thymocyte numbers in homozygous null mice are reduced to less than half the number present in wild-type control mice, whereas the numbers of either CD4/CD8 double-negative (DN) immature thymocytes or mature single-positive (SP) thymocytes remain grossly normal
• in homozygous null mice, DP thymocytes exhibit a strikingly increased susceptibility to cell death in response to both dexamethasone and irradiation due to massive apoptosis in the cortex (confirmed by TUNEL analysis)
• in vitro, recombinant CD5 antigen-like protein significantly inhibits apoptosis of DP thymocytes as well as CD95/Fas-mediated apoptosis of a monocyte-derived cell line, J774A.1, which shows high binding capacity for CD5L

immune system
N
• thymocyte development from the DN to the DP stage appears normal
• the CD4/CD8 double-positive (DP) thymocyte numbers in homozygous null mice are reduced to less than half the number present in wild-type control mice, whereas the numbers of either CD4/CD8 double-negative (DN) immature thymocytes or mature single-positive (SP) thymocytes remain grossly normal
• in homozygous null mice, DP thymocytes exhibit a strikingly increased susceptibility to cell death in response to both dexamethasone and irradiation due to massive apoptosis in the cortex (confirmed by TUNEL analysis)
• in vitro, recombinant CD5 antigen-like protein significantly inhibits apoptosis of DP thymocytes as well as CD95/Fas-mediated apoptosis of a monocyte-derived cell line, J774A.1, which shows high binding capacity for CD5L
• when injected with heat-killed Corynebacterium parvum, homozygous null mice display enhanced and prolonged bacterial-induced granuloma formation
• mutant mice exhibit increased apoptosis of natural killer T (NKT) and T cells in the early stage of hepatic granuloma formation, and delayed repopulation of NKT cells in the late stage of granuloma formation
• following C. parvum injection, most of the cytokine mRNA expression patterns are comparable between wild-type and homozygous null mice; however, IL-10 mRNA expression is less pronounced, whereas IL-12 and chemokine (C-C motif) ligand 2 (CCL2) mRNA expressions are enhanced in the liver of homozygous null mice compared with control mice
• in vitro, recombinant protein rescues the apoptosis of NKT and T cells obtained from C. parvum-injected hepatic mononuclear cells

endocrine/exocrine glands
• the CD4/CD8 double-positive (DP) thymocyte numbers in homozygous null mice are reduced to less than half the number present in wild-type control mice, whereas the numbers of either CD4/CD8 double-negative (DN) immature thymocytes or mature single-positive (SP) thymocytes remain grossly normal


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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/16/2024
MGI 6.23
The Jackson Laboratory