Literature DB >> 24832898

Characterization of FGF family growth factors concerning branching morphogenesis of mouse lung epithelium.

Asami Goto1, Naohiro Yamazaki, Hiroyuki Nogawa.   

Abstract

Mouse lung rudiments express eight members of fibroblast growth factor (FGF) family genes from embryonic day 10 (E10) to E13. Some of these are expressed in either the epithelium or mesenchyme, while others are expressed in both. Incorporating the results of our previous study, we characterized the branch-inducing activities of all of FGFs expressed in the early lung rudiment. Of these, FGF1, FGF2, FGF7, FGF9 and FGF10 induced branching morphogenesis in Matrigel-embedded E11 epithelium, and their effective concentrations varied (10 nM, 10 nM, 3 nM, 1 nM, and 100 nM, respectively). Whereas shaking culture dishes containing medium supplemented with FGF7 or FGF10 showed reduced branching morphogenesis, those supplemented with FGF1, FGF2, or FGF9 did not, suggesting the involvement of autocrine growth factor(s) in branching morphogenesis induced by FGF7 or FGF10. In the presence of heparin, a well-known activator of FGF signaling, cystic morphology with lumen expansion was observed in cultures containing FGF1, FGF7, or FGF10, but growth arrest was observed in cultures containing FGF2 or FGF9. These results indicate that several paracrine and autocrine FGFs function during branching morphogenesis of lung epithelium.

Entities:  

Keywords:  FGF; autocrine; branching morphogenesis; lung; mouse; paracrine

Mesh:

Substances:

Year:  2014        PMID: 24832898     DOI: 10.2108/zs130252

Source DB:  PubMed          Journal:  Zoolog Sci        ISSN: 0289-0003            Impact factor:   0.931


  2 in total

1.  Congenital cystic adenomatoid malformations of the lung: an epithelial transcriptomic approach.

Authors:  Guillaume Lezmi; Shamila Vibhushan; Claudia Bevilaqua; Nicolas Crapart; Nicolas Cagnard; Naziha Khen-Dunlop; Christine Boyle-Freyssaut; Alice Hadchouel; Christophe Delacourt
Journal:  Respir Res       Date:  2020-02-04

2.  FGF22 deletion causes hidden hearing loss by affecting the function of inner hair cell ribbon synapses.

Authors:  Shule Hou; Jifang Zhang; Yan Wu; Chen Junmin; Huang Yuyu; Baihui He; Yan Yang; Yuren Hong; Jiarui Chen; Jun Yang; Shuna Li
Journal:  Front Mol Neurosci       Date:  2022-07-28       Impact factor: 6.261

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.