Members of the winged helix/forkhead (~forkhead~) family of transcription factors have critical roles in the regulation of gene expression, embryogenesis and tissue differentiation. The precise regulation of gene expression in airway epithelial cells is critical in the developing, injured and diseased lung, however little is known about transcription factors that direct gene expression in airway epithelial cells. Accordingly, we have cloned hepatocyte nuclear factor-3/forkhead homologue 4 (H.H.-4), a member of the forkhead family of transcription factors with expression in the airway restricted to bronchial epithelial cells. In evaluation of H.H.-4 expression in the developing lung, we found expression was confined to the proximal airway epithelial cells and that the onset of expression uniquely occurred at the earliest stage of differentiation between proximal and distal airway epithelium (the late pseudoglandular stage). In evaluation of H.H.-4 function, we found that H.H.-4 is a potent transcriptional activator and is capable of transactivating the Clara cell secretory protein (CCP) gene, a protein with a temporal and spatial pattern of expression in airway epithelial cells tightly linked to H.H.-4. The focus of this proposal is to determine the function of H.H.-4 in the differentiation and growth of the proximal airway. Specifically, we propose to: (1) Identify the optimal DNA sequence and corresponding target genes for H.H.-4 in proximal airway epithelial cells; (2) Characterize the structural regions of H.H.-4 responsible for DNA site-specific binding, transcriptional activation and nuclear localization in airway epithelial cells; an (3) Determine of the role of H.H.-4 in the development and differentiation of the proximal airway epithelium through targeted disruption of the H.H.-4 gene to create H.H.-4 deficient mice. Determining the role of H.H.-4 in the regulation of proximal airway epithelial cells will facilitate an understanding of molecular mechanisms driving the phenotypic abnormalities of epithelial calls in lung disease.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
First Independent Research Support & Transition (FIRST) Awards (R29)
Project #
1R29HL056244-01A1
Application #
2029938
Study Section
Lung Biology and Pathology Study Section (LBPA)
Project Start
1997-01-01
Project End
2001-12-31
Budget Start
1997-01-01
Budget End
1997-12-31
Support Year
1
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Washington University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
062761671
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Rieger, Megan E; Zhou, Beiyun; Solomon, Nicola et al. (2016) p300/?-Catenin Interactions Regulate Adult Progenitor Cell Differentiation Downstream of WNT5a/Protein Kinase C (PKC). J Biol Chem 291:6569-82
Horani, Amjad; Brody, Steven L; Ferkol, Thomas W (2014) Picking up speed: advances in the genetics of primary ciliary dyskinesia. Pediatr Res 75:158-64
Horani, Amjad; Ferkol, Thomas W; Shoseyov, David et al. (2013) LRRC6 mutation causes primary ciliary dyskinesia with dynein arm defects. PLoS One 8:e59436
Horani, Amjad; Brody, Steven L; Ferkol, Thomas W et al. (2013) CCDC65 mutation causes primary ciliary dyskinesia with normal ultrastructure and hyperkinetic cilia. PLoS One 8:e72299
Vladar, Eszter K; Brody, Steven L (2013) Analysis of ciliogenesis in primary culture mouse tracheal epithelial cells. Methods Enzymol 525:285-309
Horani, Amjad; Nath, Aditya; Wasserman, Mollie G et al. (2013) Rho-associated protein kinase inhibition enhances airway epithelial Basal-cell proliferation and lentivirus transduction. Am J Respir Cell Mol Biol 49:341-7
Horani, Amjad; Druley, Todd E; Zariwala, Maimoona A et al. (2012) Whole-exome capture and sequencing identifies HEATR2 mutation as a cause of primary ciliary dyskinesia. Am J Hum Genet 91:685-93
Ibricevic, Aida; Brody, Steven L; Youngs, Wiley J et al. (2010) ATP7B detoxifies silver in ciliated airway epithelial cells. Toxicol Appl Pharmacol 243:315-22
Blatt, E N; Yan, X H; Wuerffel, M K et al. (1999) Forkhead transcription factor HFH-4 expression is temporally related to ciliogenesis. Am J Respir Cell Mol Biol 21:168-76