HOMEPRODUCTSSERVICESCOMPANYCONTACTFAQResearchDictionaryPharmaMobileSign Up FREE or Login

Apc deficiency alters pulmonary epithelial cell fate and inhibits Nkx2.1 via triggering TGF-beta signaling.

Abstract
Wnt signaling is critical for cell fate specification and cell differentiation in many organs, but its function in pulmonary neuroendocrine cell (PNEC) differentiation has not been fully addressed. In this study, we examined the role of canonical Wnt signaling by targeting the gene for Adenomatous Polyposis Coli (Apc), which controls Wnt signaling activity via mediating phosphorylation of beta-catenin (Ctnnb). Targeting the Apc gene in lung epithelial progenitors by Nkx2.1-cre stabilized Ctnnb and activated canonical Wnt signaling. Apc deficiency altered lung epithelial cell fate by inhibiting Clara and ciliated cell differentiation and activating Uchl1, a marker of neuroendocrine cells. Similar to PNEC in normal lung, Uchl1(positive) cells were innervated. In mice with targeted inactivation of Ctnnb by Nkx2.1-cre, PNEC differentiation was not interrupted. These indicate that, after lung primordium formation, Wnt signaling is not essential for PNEC differentiation; however, its over-activation promotes PNEC features. Interestingly, Nkx2.1 was extinguished in Apc deficient epithelial progenitors before activation of Uchl1. Examination of Nkx2.1 null lungs suggested that early deletion of Nkx2.1 inhibits PNEC differentiation, while late repression does not. Nkx2.1 was specifically inhibited in Apc deficient lungs but not in Ctnnb gain-of-function lungs indicating a functional difference between Apc deletion and Ctnnb stabilization, both of which activate Wnt signaling. Further analysis revealed that Apc deficiency led to increased TGF-beta signaling, which inhibited Nkx2.1 in cultured lung endodermal explants. In contrast, TGF-beta activity was not increased in Ctnnb gain-of-function lungs. Therefore, our studies revealed an important mechanism involving Apc and TGF-beta signaling in regulating the key transcriptional factor, Nkx2.1, for lung epithelial progenitor cell fate determination.
AuthorsChanggong Li, Aimin Li, Yiming Xing, Min Li, Belinda Chan, Ruoyun Ouyang, Makoto Mark Taketo, Raju Kucherlapati, Zea Borok, Parviz Minoo
JournalDevelopmental biology (Dev Biol) Vol. 378 Issue 1 Pg. 13-24 (Jun 1 2013) ISSN: 1095-564X [Electronic] United States
PMID23562608 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2013 Elsevier Inc. All rights reserved.
Chemical References
  • Adenomatous Polyposis Coli Protein
  • Nuclear Proteins
  • RNA, Messenger
  • Transcription Factors
  • Transforming Growth Factor beta
  • thyroid nuclear factor 1
Topics
  • Adenomatous Polyposis Coli Protein (physiology)
  • Animals
  • Cell Differentiation
  • Cell Lineage
  • Epithelial Cells (cytology)
  • Gene Deletion
  • Gene Expression Regulation, Developmental
  • Genes, APC
  • Lung (cytology, embryology)
  • Mice
  • Models, Biological
  • Morphogenesis
  • Nuclear Proteins (genetics, physiology)
  • RNA, Messenger (metabolism)
  • Signal Transduction
  • Stem Cells (cytology)
  • Transcription Factors (genetics, physiology)
  • Transforming Growth Factor beta (metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research network!


Choose Username:
Email:
Password:
Verify Password: