Generation and validation of novel conditional flox and inducible Cre alleles targeting fibroblast growth factor 18 (Fgf18)

被引:20
作者
Hagan, Andrew S. [1 ]
Boylan, Michael [2 ]
Smith, Craig [1 ]
Perez-Santamarina, Estela [3 ]
Kowalska, Karolina [3 ]
Hung, Irene H. [4 ]
Lewis, Renate M. [5 ]
Hajihosseini, Mohammad K. [3 ]
Lewandoski, Mark [2 ]
Ornitz, David M. [1 ]
机构
[1] Washington Univ, Sch Med, Dept Dev Biol, 3905 South Bldg,Campus Box 8103,660 S Euclid Ave, St Louis, MO 63110 USA
[2] NCI, Canc & Dev Biol Lab, NIH, Frederick, MD 21701 USA
[3] Univ East Anglia, Sch Biol Sci, Norwich, Norfolk, England
[4] Univ Utah, Sch Med, Dept Neurobiol & Anat, Salt Lake City, UT USA
[5] Washington Univ, Sch Med, Dept Neurol, St Louis, MO 63110 USA
基金
英国生物技术与生命科学研究理事会; 美国国家卫生研究院;
关键词
bone development; Cre-lox recombination; FGF signaling; knock in mice; reporter gene; CHONDROCYTE PROLIFERATION; RECEPTOR SPECIFICITY; FACTOR FAMILY; EXPRESSION; DIFFERENTIATION; FGF-18; LUNG; INACTIVATION; OSTEOGENESIS; MESODERM;
D O I
10.1002/dvdy.85
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Background Fibroblast growth factor 18 (FGF18) functions in the development of several tissues, including the lung, limb bud, palate, skeleton, central nervous system, and hair follicle. Mice containing a germline knockout of Fgf18 (Fgf18(-/-)) die shortly after birth. Postnatally, FGF18 is being evaluated for pathogenic roles in fibrosis and several types of cancer. The specific cell types that express FGF18 have been difficult to identify, and the function of FGF18 in postnatal development and tissue homeostasis has been hampered by the perinatal lethality of Fgf18 null mice. Results We engineered a floxed allele of Fgf18 (Fgf18(flox)) that allows conditional gene inactivation and a CreER(T2) knockin allele (Fgf18(CreERT2)) that allows the precise identification of cells that express Fgf18 and their lineage. We validated the Fgf18(flox) allele by targeting it in mesenchymal tissue and primary mesoderm during embryonic development, resulting in similar phenotypes to those observed in Fgf18 null mice. We also use the Fgf18(CreERT2) allele, in combination with a conditional fluorescent reporter to confirm known and identify new sites of Fgf18 expression. Conclusion These alleles will be useful to investigate FGF18 function during organogenesis and tissue homeostasis, and to target specific cell lineages at embryonic and postnatal time points.
引用
收藏
页码:882 / 893
页数:12
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