Literature DB >> 9500294

Elimination of neutrophils by apoptosis during the resolution of acute pulmonary inflammation in rats.

Y Ishii1, K Hashimoto, A Nomura, T Sakamoto, Y Uchida, M Ohtsuka, S Hasegawa, M Sagai.   

Abstract

We evaluated the apoptosis of neutrophils during the resolution of acute pulmonary inflammation induced by exposure to ozone. The inflammatory response was assessed in rat lungs 0, 1, 3, and 7 days after 4-h exposure to air or 2 ppm ozone. Analysis of bronchoalveolar lavage fluid demonstrated significant increases in albumin concentrations on days 0 and 1 and in the number of lavageable neutrophils on days 0, 1, and 3, indicating the presence of acute pulmonary inflammation. These parameters returned to control values on day 7, which suggests that the acute pulmonary inflammation induced by ozone was reversible. On days 1 and 3, but not on day 0, the neutrophils showed morphologic evidence of apoptosis. Based on morphologic analysis, the proportion of apoptotic neutrophils was 23.3 +/- 2.2% on day 1 and 55.7 +/- 3.2% on day 3. Terminal deoxynucleotidyl transferase-mediated dUTP end labeling (TUNEL), in contrast, revealed that the proportion of apoptotic cells was 59.7 +/- 9.1% on day 1 and 68.0 +/- 4.3% on day 3. On day 3, light microscopy and electron microscopy demonstrated engulfment of the neutrophils by macrophages. These findings indicate that the apoptosis of neutrophils followed by their engulfment by macrophages contributes to the clearance of neutrophils from the sites of inflammation. Moreover, TUNEL detected apoptotic neutrophils with greater sensitivity compared with morphologic assessment.

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Year:  1998        PMID: 9500294     DOI: 10.1007/pl00007597

Source DB:  PubMed          Journal:  Lung        ISSN: 0341-2040            Impact factor:   2.584


  15 in total

1.  Ozone inhalation promotes CX3CR1-dependent maturation of resident lung macrophages that limit oxidative stress and inflammation.

Authors:  Robert M Tighe; Zhuowei Li; Erin N Potts; Sarah Frush; Ningshan Liu; Michael D Gunn; W Michael Foster; Paul W Noble; John W Hollingsworth
Journal:  J Immunol       Date:  2011-09-19       Impact factor: 5.422

2.  Classical and alternative macrophage activation in the lung following ozone-induced oxidative stress.

Authors:  Vasanthi R Sunil; Kinal Patel-Vayas; Jianliang Shen; Jeffrey D Laskin; Debra L Laskin
Journal:  Toxicol Appl Pharmacol       Date:  2012-06-19       Impact factor: 4.219

3.  Regulation of ozone-induced lung inflammation and injury by the β-galactoside-binding lectin galectin-3.

Authors:  Vasanthi R Sunil; Mary Francis; Kinal N Vayas; Jessica A Cervelli; Hyejeong Choi; Jeffrey D Laskin; Debra L Laskin
Journal:  Toxicol Appl Pharmacol       Date:  2015-02-25       Impact factor: 4.219

4.  Poly(ADP-ribosyl)ation of high mobility group box 1 (HMGB1) protein enhances inhibition of efferocytosis.

Authors:  Kasey Davis; Sami Banerjee; Arnaud Friggeri; Celeste Bell; Edward Abraham; Mourad Zerfaoui
Journal:  Mol Med       Date:  2012-05-09       Impact factor: 6.354

Review 5.  Lung macrophages: current understanding of their roles in Ozone-induced lung diseases.

Authors:  Sonika Patial; Yogesh Saini
Journal:  Crit Rev Toxicol       Date:  2020-05-27       Impact factor: 5.635

Review 6.  Genes of innate immunity and the biological response to inhaled ozone.

Authors:  Zhuowei Li; Robert M Tighe; Feifei Feng; Julie G Ledford; John W Hollingsworth
Journal:  J Biochem Mol Toxicol       Date:  2012-11-20       Impact factor: 3.642

7.  Deficient in vitro and in vivo phagocytosis of apoptotic T cells by resident murine alveolar macrophages.

Authors:  B Hu; J Sonstein; P J Christensen; A Punturieri; J L Curtis
Journal:  J Immunol       Date:  2000-08-15       Impact factor: 5.422

8.  High mobility group protein-1 inhibits phagocytosis of apoptotic neutrophils through binding to phosphatidylserine.

Authors:  Gang Liu; Jing Wang; Young-Jun Park; Yuko Tsuruta; Emmanuel F Lorne; Xia Zhao; Edward Abraham
Journal:  J Immunol       Date:  2008-09-15       Impact factor: 5.422

9.  Acute alcohol intake impairs lung inflammation by changing pro- and anti-inflammatory mediator balance.

Authors:  Nympha B D'Souza El-Guindy; Willem J de Villiers; Dennis E Doherty
Journal:  Alcohol       Date:  2007-08       Impact factor: 2.405

10.  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

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