FGF signaling in mammary gland fibroblasts regulates multiple fibroblast functions and mammary epithelial morphogenesis.
Animals
Female
Fibroblast Growth Factor 2
/ metabolism
Fibroblast Growth Factor 9
/ metabolism
Fibroblasts
/ cytology
MAP Kinase Signaling System
Mammary Glands, Animal
/ cytology
Mice
Mice, Inbred ICR
Paracrine Communication
Receptor, Fibroblast Growth Factor, Type 1
/ metabolism
Receptor, Fibroblast Growth Factor, Type 2
/ metabolism
Branching morphogenesis
Collagen
Extracellular matrix
Fibroblast
Fibroblast growth factor
Mammary gland
Mouse
Stroma
Journal
Development (Cambridge, England)
ISSN: 1477-9129
Titre abrégé: Development
Pays: England
ID NLM: 8701744
Informations de publication
Date de publication:
02 12 2019
02 12 2019
Historique:
received:
03
10
2019
accepted:
24
10
2019
pubmed:
9
11
2019
medline:
24
6
2020
entrez:
9
11
2019
Statut:
epublish
Résumé
Fibroblast growth factor (FGF) signaling is crucial for mammary gland development. Although multiple roles for FGF signaling in the epithelium have been described, the function of FGF signaling in mammary stroma has not been elucidated. In this study, we investigated FGF signaling in mammary fibroblasts. We found that murine mammary fibroblasts express FGF receptors FGFR1 and FGFR2 and respond to FGF ligands. In particular, FGF2 and FGF9 induce sustained ERK1/2 signaling and promote fibroblast proliferation and migration in 2D cultures. Intriguingly, only FGF2 induces fibroblast migration in 3D extracellular matrix (ECM) through regulation of actomyosin cytoskeleton and promotes force-mediated collagen remodeling by mammary fibroblasts. Moreover, FGF2 regulates production of ECM proteins by mammary fibroblasts, including collagens, fibronectin, osteopontin and matrix metalloproteinases. Finally, using organotypic 3D co-cultures we show that FGF2 and FGF9 signaling in mammary fibroblasts enhances fibroblast-induced branching of mammary epithelium by modulating paracrine signaling, and that knockdown of
Identifiants
pubmed: 31699800
pii: dev.185306
doi: 10.1242/dev.185306
pii:
doi:
Substances chimiques
Fgf9 protein, mouse
0
Fibroblast Growth Factor 9
0
Fibroblast Growth Factor 2
103107-01-3
Fgfr1 protein, mouse
EC 2.7.10.1
Fgfr2 protein, mouse
EC 2.7.10.1
Receptor, Fibroblast Growth Factor, Type 1
EC 2.7.10.1
Receptor, Fibroblast Growth Factor, Type 2
EC 2.7.10.1
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
© 2019. Published by The Company of Biologists Ltd.
Déclaration de conflit d'intérêts
Competing interestsThe authors declare no competing or financial interests.