Journal article

Impaired TLR4 and HIF expression in cystic fibrosis bronchial epithelial cells downregulates hemeoxygenase-1 and alters iron homeostasis in vitro


Authors listChillappagari, Shashi; Venkatesan, Shalini; Garapati, Virajith; Mahavadi, Poornima; Munder, Antje; Seubert, Andreas; Sarode, Gaurav; Guenther, Andreas; Schmeck, Bernd T.; Tuemmler, Burkhard; Henke, Markus O.

Publication year2014

PagesL791-L799

JournalAmerican Journal of Physiology - Lung Cellular and Molecular Physiology

Volume number307

Issue number10

ISSN1040-0605

eISSN1522-1504

DOI Linkhttps://doi.org/10.1152/ajplung.00167.2014

PublisherAmerican Physiological Society


Abstract
Hemeoxygenase-1 (HO-1), an inducible heat shock protein, is upregulated in response to multiple cellular insults via oxidative stress, lipopolysaccharides (LPS), and hypoxia. In this study, we investigated in vitro the role of Toll-like receptor 4 (TLR4), hypoxia-inducible factor 1 alpha (HIF-1 alpha), and iron on HO-1 expression in cystic fibrosis (CF). Immunohistochemical analysis of TLR4, HO-1, ferritin, and HIF-1 alpha were performed on lung sections of CFTR-/- and wild-type mice. CFBE41o- and 16HBE14o- cell lines were employed for in vitro analysis via immunoblotting, immunofluorescence, real-time PCR, luciferase reporter gene analysis, and iron quantification. We observed a reduced TLR4, HIF-1 alpha, HO-1, and ferritin in CFBE41o- cell line and CF mice. Knockdown studies using TLR4-siRNA in 16HBE14o- revealed significant decrease of HO-1, confirming the role of TLR4 in HO-1 downregulation. Inhibition of HO-1 using tin protoporphyrin in 16HBE14o- cells resulted in increased iron levels, suggesting a probable role of HO-1 in iron accumulation. Additionally, sequestration of excess iron using iron chelators resulted in increased hypoxia response element response in CFBE41o- and 16HBE14o-, implicating a role of iron in HIF-1 alpha stabilization and HO-1. To conclude, our in vitro results demonstrate that multiple regulatory factors, such as impaired TLR4 surface expression, increased intracellular iron, and decreased HIF-1 alpha, downregulate HO-1 expression in CFBE41o- cells.



Citation Styles

Harvard Citation styleChillappagari, S., Venkatesan, S., Garapati, V., Mahavadi, P., Munder, A., Seubert, A., et al. (2014) Impaired TLR4 and HIF expression in cystic fibrosis bronchial epithelial cells downregulates hemeoxygenase-1 and alters iron homeostasis in vitro, American Journal of Physiology - Lung Cellular and Molecular Physiology, 307(10), pp. L791-L799. https://doi.org/10.1152/ajplung.00167.2014

APA Citation styleChillappagari, S., Venkatesan, S., Garapati, V., Mahavadi, P., Munder, A., Seubert, A., Sarode, G., Guenther, A., Schmeck, B., Tuemmler, B., & Henke, M. (2014). Impaired TLR4 and HIF expression in cystic fibrosis bronchial epithelial cells downregulates hemeoxygenase-1 and alters iron homeostasis in vitro. American Journal of Physiology - Lung Cellular and Molecular Physiology. 307(10), L791-L799. https://doi.org/10.1152/ajplung.00167.2014



Keywords


Cystic fibrosishypoxia-inducible factorhypoxia-inducible factor 1 alphaLUNG-DISEASETOLL-LIKE RECEPTORToll-like receptor 4

Last updated on 2025-21-05 at 18:36