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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Ccl17tm2.1(cre)Ifo
targeted mutation 2.1, Irmgard Foerster
MGI:5438830
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Ccl17tm2.1(cre)Ifo/Ccl17+
Hif1atm3Rsjo/Hif1atm3Rsjo
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:5545808


Genotype
MGI:5545808
cn1
Allelic
Composition
Ccl17tm2.1(cre)Ifo/Ccl17+
Hif1atm3Rsjo/Hif1atm3Rsjo
Genetic
Background
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ccl17tm2.1(cre)Ifo mutation (0 available); any Ccl17 mutation (11 available)
Hif1atm3Rsjo mutation (3 available); any Hif1a mutation (50 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
N
• bone marrow derived dendritic cells (BMDCs) cultured under hypoxic conditions (1% oxygen) show upregulation of maturation markers such as MHCII, CD86, with CD80 only slightly enhanced; control BMDCs grown in hypoxic conditions show similar enhanced maturation markers
• cytokine production is reduced in mutant and control BMDCs under hypoxic conditions; production of Il12p70, Il10, Il6, and Il23 is decreased in mutant and control BMDCs under hypoxic conditions, with Il22 upregulated compared to normoxic cells
• stimulation by LPS does not further enhance expression of maturation markers as it does in BMDCs grown under normoxic conditions
• production of Il12p70, Il10, Il6, and Il23 is decreased in mutant and control BMDCs under hypoxic conditions, with Il22 upregulated compared to normoxic cells
• fewer mutant BMDCs generated under hypoxic conditions migrate toward CCL19 in a transwell chamber assay than control cells grown under hypoxic conditions or mutant and control cells generated under normoxic conditions; migration toward CXCL12 is not different from controls under hypoxic or normoxic conditions
• bone marrow dendritic cells (BMDCs) differentiated under hypoxic conditions in culture display reduced growth (proliferation) compared to control cells grown in hypoxia or mutant cells grown under normoxic (21% oxygen) conditions
• BMDCs produce similar levels of Il-1b under hypoxic and normoxic conditions while control cells and BMDCs with CD11c-driven Hif1a deletion show decreased production under hypoxic conditions
• BMDCs produce similar levels of TNFalpha under hypoxic and normoxic conditions while control cells and BMDCs with CD11c-driven Hif1a deletion show decreased production under hypoxic conditions

cellular
• reduced amounts of ATP are detected in lysates of mutant BMDCs cultured under hypoxic conditions compared to control cells under hypoxia suggesting an energy metabolism defect with Hif1a deletion
• fewer mutant BMDCs generated under hypoxic conditions migrate toward CCL19 in a transwell chamber assay than control cells grown under hypoxic conditions or mutant and control cells generated under normoxic conditions; migration toward CXCL12 is not different from controls under hypoxic or normoxic conditions

hematopoietic system
• fewer mutant BMDCs generated under hypoxic conditions migrate toward CCL19 in a transwell chamber assay than control cells grown under hypoxic conditions or mutant and control cells generated under normoxic conditions; migration toward CXCL12 is not different from controls under hypoxic or normoxic conditions
• bone marrow dendritic cells (BMDCs) differentiated under hypoxic conditions in culture display reduced growth (proliferation) compared to control cells grown in hypoxia or mutant cells grown under normoxic (21% oxygen) conditions





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
11/19/2024
MGI 6.24
The Jackson Laboratory