Document Detail


Stretch-induced fetal type II cell differentiation is mediated via ErbB1-ErbB4 interactions.
MedLine Citation:
PMID:  22493501     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Stretch-induced differentiation of lung fetal type II epithelial cells is mediated through EGFR (ErbB1) via release of HB-EGF and TGF-α ligands. Employing an EGFR knock-out mice model, we further investigated the role of the ErbB family of receptors in mechanotranduction during lung development. Deletion of EGFR prevented endogenous and mechanical stretch-induced type II cell differentiation via the ERK pathway, which was rescued by overexpression of a constitutively active MEK. Interestingly, the expression of ErbB4, the only ErbB receptor that EGFR co-precipitates in wild-type cells, was decreased in EGFR-deficient type II cells. Similar to EGFR, ErbB4 was activated by stretch and participated in ERK phosphorylation and type II cell differentiation. However, neuregulin (NRG) or stretch-induced ErbB4 activation were blunted in EGFR-deficient cells and not rescued after ErbB4 overexpression, suggesting that induction of ErbB4 phosphorylation is EGFR-dependent. Finally, we addressed how shedding of ligands is regulated by EGFR. In knock-out cells, TGF-α, a ligand for EGFR, was not released by stretch, while HB-EGF, a ligand for EGFR and ErbB4, was shed by stretch although to a lower magnitude than in normal cells. Release of these ligands was inhibited by blocking EGFR and ERK pathway. In conclusion, our studies show that EGFR and ErbB4 regulate stretch-induced type II cell differentiation via ERK pathway. Interactions between these two receptors are important for mechanical signals in lung fetal type II cells. These studies provide novel insights into the cell signaling mechanisms regulating ErbB family receptors in lung cell differentiation.
Authors:
Zheping Huang; Yulian Wang; Pritha S Nayak; Christiane E Dammann; Juan Sanchez-Esteban
Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural     Date:  2012-04-09
Journal Detail:
Title:  The Journal of biological chemistry     Volume:  287     ISSN:  1083-351X     ISO Abbreviation:  J. Biol. Chem.     Publication Date:  2012 May 
Date Detail:
Created Date:  2012-05-28     Completed Date:  2012-08-15     Revised Date:  2013-06-26    
Medline Journal Info:
Nlm Unique ID:  2985121R     Medline TA:  J Biol Chem     Country:  United States    
Other Details:
Languages:  eng     Pagination:  18091-102     Citation Subset:  IM    
Affiliation:
Department of Pediatrics, Women & Infants Hospital of Rhode Island and the Warren Alpert Medical School of Brown University, Providence, Rhode Island 02905, USA.
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MeSH Terms
Descriptor/Qualifier:
Animals
Base Sequence
Cell Differentiation / physiology*
DNA Primers
Extracellular Signal-Regulated MAP Kinases / metabolism
Female
Fetus / cytology*
Mechanotransduction, Cellular / physiology*
Mice
Mice, Knockout
Pregnancy
Protein Binding
Real-Time Polymerase Chain Reaction
Receptor, Epidermal Growth Factor / genetics,  metabolism,  physiology*
Grant Support
ID/Acronym/Agency:
P20 RR018728/RR/NCRR NIH HHS; R01 HD052670/HD/NICHD NIH HHS
Chemical
Reg. No./Substance:
0/DNA Primers; EC 2.7.10.1/Receptor, Epidermal Growth Factor; EC 2.7.10.1/receptor tyrosine-protein kinase erbB-4; EC 2.7.11.24/Extracellular Signal-Regulated MAP Kinases
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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