Respiratory tract responses to dust: Relationships between dust burden, lung injury, alveolar macrophage fibronectin release, and the development of pulmonary fibrosis

Kevin E. Driscoll, James K. Maurer, Robert C. Lindenschmidt, Debra Romberger, Stephen I. Rennard, Leslie Crosby

Research output: Contribution to journalArticle

75 Scopus citations

Abstract

A multidisciplinary approach was used to investigate the responses of the respiratory tract to silica (SiO2) or titanium dioxide (TiO2). Rats were intratracheally instilled with 5-100 mg/kg of dust and bronchoalveolar lavage fluid (BALF) lactate dehydrogenase (LDH) and total protein (TP) and ex vivo alveolar macrophage (AM) fibronectin release assessed on Days 7, 14, and 28 after exposure. Lung dust burdens were determined on Days 1, 7, and 28 after instillation. Both dusts elicited dose-related increases in BALF LDH and TP, a response which was more pronounced and progressive with SiO2. All doses of SiO2 elicited persistent increases in AM fibronectin release. TiO2 stimulated persistent increases in AM fibronectin release at ≥ 50 mg/kg, with transient or no effect at ≤ 10 mg/kg. Increased SiO2 retention was observed for all doses and TiO2 retention was increased only at doses ≥ 50 mg/kg. In vitro exposure of naive AM to SiO2 or TiO2 did not stimulate AM fibronectin release. Histopathology demonstrated fibrosis at all SiO2 doses; only TiO2 doses ≥ 50 mg/kg resulted in fibrosis. These results reveal an association between increased dust retention, lung injury, activation of AM fibronectin release, and the development of fibrosis. The magnitude and temporal pattern of responses clearly differentiated SiO2 from TiO2. The correlation of BALF markers of lung injury and increased AM fibronectin release with the development of fibrosis supports the use of these parameters as predictive biomarkers of dust-induced interstitial lung disease.

Original languageEnglish (US)
Pages (from-to)88-101
Number of pages14
JournalToxicology and Applied Pharmacology
Volume106
Issue number1
DOIs
StatePublished - Oct 1990

ASJC Scopus subject areas

  • Toxicology
  • Pharmacology

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