Literature DB >> 1581072

Ozone-induced acute tracheobronchial epithelial injury: relationship to granulocyte emigration in the lung.

D M Hyde1, W C Hubbard, V Wong, R Wu, K Pinkerton, C G Plopper.   

Abstract

To investigate the relationship between granulocyte emigration and epithelial injury in specific airway generations of the tracheobronchial tree following short-term ozone exposure, we exposed rhesus monkeys for 8 h to 0.00 (controls) or 0.96 ppm ozone with post-exposure periods of 1, 12, 24, 72, and 168 h in filtered air before necropsy. There were five control and three exposed monkeys for each of the post-exposure times for a total of 20 monkeys. Neutrophils isolated from peripheral blood and labeled with 111In-tropolonate were infused in the cephalic vein in unanesthetized monkeys (except the 1-h group) 4 to 5 h before necropsy. The trachea and microdissected bronchi (fourth and ninth generations) and respiratory bronchioles (fifteenth generation) from the right upper lobe of each monkey were examined by electron microscopy. Labeled neutrophil influx into lung tissue and bronchoalveolar lavage fluid (BALF) was maximal at 12 h and returned to baseline by 24 h after exposure. This was in contrast to total neutrophils (labeled and unlabeled) in BALF, which were significantly elevated through 24 h after exposure but returned to baseline by 72 h. Lavage protein was significantly elevated at 24 h after exposure but was at control levels at all other times. Morphometric observations showed epithelial necrosis at 1 and 12 h in the trachea and bronchioles but continued to be observed in significant numbers at 24 h after exposure in bronchi. A significant increase in the labeling index of epithelial cells was observed at 12 h only in bronchi. Epithelial necrosis and repair was associated with the presence of granulocytes in the epithelium and interstitium of all airway levels. However, eosinophils were maximally increased in the epithelium and interstitium of bronchi at 24 h after exposure when epithelial necrosis was maximal in these airways and when lavage protein was significantly elevated.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1992        PMID: 1581072     DOI: 10.1165/ajrcmb/6.5.481

Source DB:  PubMed          Journal:  Am J Respir Cell Mol Biol        ISSN: 1044-1549            Impact factor:   6.914


  19 in total

1.  Postnatal episodic ozone results in persistent attenuation of pulmonary and peripheral blood responses to LPS challenge.

Authors:  Kinjal Maniar-Hew; Edward M Postlethwait; Michelle V Fanucchi; Carol A Ballinger; Michael J Evans; Jack R Harkema; Stephan A Carey; Ruth J McDonald; Alfred A Bartolucci; Lisa A Miller
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2010-12-03       Impact factor: 5.464

2.  Inhibition of myristoylated alanine-rich C kinase substrate (MARCKS) protein inhibits ozone-induced airway neutrophilia and inflammation.

Authors:  Gautam Damera; William F Jester; Meiqi Jiang; Hengjiang Zhao; Homer W Fogle; Michael Mittelman; Angela Haczku; Edwin Murphy; Indu Parikh; Reynold A Panettieri
Journal:  Exp Lung Res       Date:  2010-03       Impact factor: 2.459

3.  Increased CCL24/eotaxin-2 with postnatal ozone exposure in allergen-sensitized infant monkeys is not associated with recruitment of eosinophils to airway mucosa.

Authors:  Debbie L Chou; Joan E Gerriets; Edward S Schelegle; Dallas M Hyde; Lisa A Miller
Journal:  Toxicol Appl Pharmacol       Date:  2011-09-12       Impact factor: 4.219

Review 4.  Plasma membrane wounding and repair in pulmonary diseases.

Authors:  Xiaofei Cong; Rolf D Hubmayr; Changgong Li; Xiaoli Zhao
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2017-01-06       Impact factor: 5.464

5.  Hyaluronan mediates airway hyperresponsiveness in oxidative lung injury.

Authors:  Ahmed Lazrak; Judy Creighton; Zhihong Yu; Svetlana Komarova; Stephen F Doran; Saurabh Aggarwal; Charles W Emala; Vandy P Stober; Carol S Trempus; Stavros Garantziotis; Sadis Matalon
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2015-03-06       Impact factor: 5.464

Review 6.  Utility of large-animal models of BPD: chronically ventilated preterm lambs.

Authors:  Kurt H Albertine
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2015-03-13       Impact factor: 5.464

7.  Interaction of rat alveolar macrophages with pulmonary epithelial cells following exposure to lipopolysaccharide.

Authors:  S Hirano
Journal:  Arch Toxicol       Date:  1996       Impact factor: 5.153

8.  Dose-dependent tolerance to ozone. I. Tracheobronchial epithelial reorganization in rats after 20 months' exposure.

Authors:  C G Plopper; F P Chu; C J Haselton; J Peake; J Wu; K E Pinkerton
Journal:  Am J Pathol       Date:  1994-02       Impact factor: 4.307

9.  IL-1 receptors mediate persistent, but not acute, airway hyperreactivity to ozone in guinea pigs.

Authors:  Kirsten C Verhein; David B Jacoby; Allison D Fryer
Journal:  Am J Respir Cell Mol Biol       Date:  2008-07-10       Impact factor: 6.914

10.  Effect of host modification and age on airway epithelial gene transfer mediated by a murine leukemia virus-derived vector.

Authors:  L G Johnson; J P Mewshaw; H Ni; T Friedmann; R C Boucher; J C Olsen
Journal:  J Virol       Date:  1998-11       Impact factor: 5.103

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