Abstract
Colony stimulating factor-1 (CSF-1) is the primary regulator of the mononuclear phagocytic lineage acting through its transmembrane tyrosine kinase receptor, CSF-1R, that is the product of the c-fms protooncogene. Null mutations in either the ligand or the receptor genes result in a severe osteopetrosis as well as a number of other phenotypes, including reproductive defects and perturbations in organ development. The CSF-1R is also expressed in oocytes, myoblast progenitors, decidual, and trophoblastic cells. To distinguish cell type specific phenotypes, we have created a conditional allele of the Csf1r by placing LoxP sites around Exon 5 of the Csf1r gene in mice. Excision of this floxed sequence results in a null allele that in the homozygous state gives a phenotype indistinguishable of the complete Csf1r null mutant mouse. This conditional allele will prove extremely valuable to study the spatial and temporal roles of CSF-1R.
Original language | English (US) |
---|---|
Pages (from-to) | 328-335 |
Number of pages | 8 |
Journal | Genesis |
Volume | 44 |
Issue number | 7 |
DOIs | |
State | Published - Jul 2006 |
Keywords
- CSF-1
- M-CSF
- Macrophages
- Reproduction
ASJC Scopus subject areas
- Genetics
- Endocrinology
- Cell Biology