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NDRG1 is important to maintain the integrity of airway epithelial barrier through claudin-9 expression
- Source :
- Cell Biology International. 41:716-725
- Publication Year :
- 2017
- Publisher :
- Wiley, 2017.
-
Abstract
- Impairment of epithelial barrier integrity caused by environmental triggers is associated with the pathogenesis of airway inflammation. Using human airway epithelial cells, we attempted to identify molecule(s) that promote airway epithelial barrier integrity. Microarray analyses were conducted using the Affimetrix human whole genome gene chip, and we identified the N-myc downstream-regulated gene 1 (NDRG1) gene, which was induced during the development of the epithelial cell barrier. Immunohistochemical analysis revealed strong NDRG1 expression in ciliated epithelial cells in nasal tissues sampled from patients with chronic rhinosinusitis (CRS), and the low expression of NDRG1 was observed in goblet cells or damaged epithelial cells. NDRG1 gene knockdown with its specific siRNA decreased the transepithelial electrical resistance and increased the dextran permeability. Immunocytochemistry revealed that NDRG1 knockdown disrupted tight junctions of airway epithelial cells. Next, we analyzed the effects of NDRG1 knockdown on the expression of tight and adhesion junction molecules. NDRG1 knockdown significantly decreased only claudin-9 expression, but did not decrease other claudin family molecules, such as E-cadherin, and ZO-1, -2, or -3. Knockdown of claudin-9 markedly impaired the barrier function in airway epithelial cells. These results suggest that NDRG1 is important for the barrier integrity in airway epithelial cells.
- Subjects :
- 0301 basic medicine
Gene knockdown
Tight junction
Chemistry
Immunocytochemistry
Cell Biology
General Medicine
respiratory system
Epithelium
Cell biology
Pathogenesis
03 medical and health sciences
030104 developmental biology
0302 clinical medicine
medicine.anatomical_structure
030220 oncology & carcinogenesis
medicine
Claudin
Barrier function
NDRG1 Gene
Subjects
Details
- ISSN :
- 10656995
- Volume :
- 41
- Database :
- OpenAIRE
- Journal :
- Cell Biology International
- Accession number :
- edsair.doi...........77648370455c15b9162f3db5eac6e457
- Full Text :
- https://doi.org/10.1002/cbin.10741