Organic dust inhibits surfactant protein expression by reducing thyroid transcription factor-1 levels in human lung epithelial cells. Issue 2 (February 2019)

• Record Type: Journal Article
• Authors: Natarajan, Kartiga; Gangam, Keerthi; Meganathan, Velmurugan; Gottipati, Koteswara R; Mitchell, Courtney; Boggaram, Vijay
• Is Part Of: Innate immunity. Volume 25:Issue 2(2019:Feb.)
• Page Start: 118
• Page End: 131
• Publication Date: 2019-02
• Subjects: Lung surfactant -- lung epithelial cells -- organic dust -- lung inflammation -- respiratory diseases; Natural immunity -- Periodicals; Endotoxins -- Periodicals; 616.07905
• DOI: 10.1177/1753425919827360
• Languages: English
• ISSNs: 1753-4259

Abstract

Exposure to organic dust is a risk factor for the development of respiratory diseases. Surfactant proteins (SP) reduce alveolar surface tension and modulate innate immune responses to control lung inflammation. Therefore, changes in SP levels could contribute to the development of organic-dust-induced respiratory diseases. Because information on the effects of organic dust on SP levels is lacking, we studied the effects of dust from a poultry farm on SP expression. We found that dust extract reduced SP-A and SP-B mRNA and protein levels in H441 human lung epithelial cells by inhibiting their promoter activities, but did not have any effect on SP-D protein levels. Dust extract also reduced SP-A and SP-C levels in primary human alveolar epithelial cells. The inhibitory effects were not due to LPS or protease activities present in dust extract or mediated via oxidative stress, but were dependent on a heat-labile factor(s). Thyroid transcription factor-1, a key transcriptional activator of SP expression, was reduced in dust-extract-treated cells, indicating that its down-regulation mediates inhibition of SP levels. Our study implies that down-regulation of SP levels by organic dust could contribute to the development of lung inflammation and respiratory diseases in humans.