SPRY1 regulates mammary epithelial morphogenesis by modulating EGFR-dependent stromal paracrine signaling and ECM remodeling
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem
Grantová podpora
R01 DE021420
NIDCR NIH HHS - United States
R03 HD060807
NICHD NIH HHS - United States
R01 CA057621
NCI NIH HHS - United States
Wellcome Trust - United Kingdom
2014NOVSP444
Breast Cancer Now - United Kingdom
MR/L011840/1
Medical Research Council - United Kingdom
PubMed
27621461
PubMed Central
PMC5047180
DOI
10.1073/pnas.1611532113
PII: 1611532113
Knihovny.cz E-zdroje
- Klíčová slova
- EGF signaling, FGF signaling, branching morphogenesis, epithelial–stromal interactions, stromal microenvironment,
- MeSH
- adaptorové proteiny signální transdukční nedostatek metabolismus MeSH
- amfiregulin farmakologie MeSH
- buňky stromatu účinky léků metabolismus MeSH
- časosběrné zobrazování MeSH
- epitel růst a vývoj metabolismus MeSH
- epitelové buňky cytologie účinky léků MeSH
- erbB receptory metabolismus MeSH
- extracelulární matrix metabolismus MeSH
- extracelulárním signálem regulované MAP kinasy metabolismus MeSH
- fibroblasty účinky léků metabolismus MeSH
- fosfoproteiny nedostatek metabolismus MeSH
- fosforylace účinky léků MeSH
- kolagen metabolismus MeSH
- ligandy MeSH
- membránové proteiny nedostatek metabolismus MeSH
- mléčné žlázy zvířat účinky léků metabolismus MeSH
- morfogeneze * účinky léků MeSH
- mutace genetika MeSH
- myši knockoutované MeSH
- myši nahé MeSH
- parakrinní signalizace * účinky léků MeSH
- pohyb buněk účinky léků MeSH
- protoonkogenní proteiny c-akt metabolismus MeSH
- signální transdukce * účinky léků MeSH
- transformující růstový faktor alfa farmakologie MeSH
- vývojová regulace genové exprese účinky léků MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
- Názvy látek
- adaptorové proteiny signální transdukční MeSH
- amfiregulin MeSH
- erbB receptory MeSH
- extracelulárním signálem regulované MAP kinasy MeSH
- fosfoproteiny MeSH
- kolagen MeSH
- ligandy MeSH
- membránové proteiny MeSH
- protoonkogenní proteiny c-akt MeSH
- Spry1 protein, mouse MeSH Prohlížeč
- transformující růstový faktor alfa MeSH
The role of the local microenvironment in influencing cell behavior is central to both normal development and cancer formation. Here, we show that sprouty 1 (SPRY1) modulates the microenvironment to enable proper mammary branching morphogenesis. This process occurs through negative regulation of epidermal growth factor receptor (EGFR) signaling in mammary stroma. Loss of SPRY1 resulted in up-regulation of EGFR-extracellular signal-regulated kinase (ERK) signaling in response to amphiregulin and transforming growth factor alpha stimulation. Consequently, stromal paracrine signaling and ECM remodeling is augmented, leading to increased epithelial branching in the mutant gland. By contrast, down-regulation of EGFR-ERK signaling due to gain of Sprouty function in the stroma led to stunted epithelial branching. Taken together, our results show that modulation of stromal paracrine signaling and ECM remodeling by SPRY1 regulates mammary epithelial morphogenesis during postnatal development.
Department of Anatomy University of California San Francisco CA 94143
School of Life Science and Technology ShanghaiTech University Shanghai 201210 China;
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