Research Project
Grant-in-Aid for Young Scientists (B)
In order to understand the mechanism of pulmonary cyst formation in Birt-Hogg-Dube(BHD) syndrome, I examined the germline FLCN mutation in patients with BHDS and functional assay of lung fibroblasts isolated from patients with BHDS. Germline FLCN mutations I identified distributed all exons of the FLCN gene, but four mutations were frequently demonstrated in our Japanese BHDS patients. Genotype-phenotype correlation is currently under investigation. As for functional analysis of BHDS lung fibroblasts, I examined proliferation and the ability of migration and gel contraction. As compared with human fetal lung fibroblasts(HFL), lung fibroblasts from BHDS showed decreased migration toward fibronectin while proliferation and gel contraction ability was similar to those with HFL. In addition, the expression of TGF beta 1, fibronectin, type I collagen was decreased in BHDS lung fibroblasts when determined by real-time PCR.
All 2011 2010 Other
All Journal Article (3 results) (of which Peer Reviewed: 3 results) Presentation (1 results) Remarks (2 results)
Eur J Radiol
Volume: 77(3) Pages: 403-9
Volume: 77/3 Issue: 3 Pages: 403-9
10.1016/j.ejrad.2009.09.004
Journal of Medical Genetics
Volume: 47(4) Pages: 281-7
http://www.lungcare.jp/index.html