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Resistin deficiency in mice has no effect on pulmonary responses induced by acute ozone exposure.


ABSTRACT: Acute exposure to ozone (O3), an air pollutant, causes pulmonary inflammation, airway epithelial desquamation, and airway hyperresponsiveness (AHR). Pro-inflammatory cytokines-including IL-6 and ligands of chemokine (C-X-C motif) receptor 2 [keratinocyte chemoattractant (KC) and macrophage inflammatory protein (MIP)-2], TNF receptor 1 and 2 (TNF), and type I IL-1 receptor (IL-1? and IL-1?)-promote these sequelae. Human resistin, a pleiotropic hormone and cytokine, induces expression of IL-1?, IL-1?, IL-6, IL-8 (the human ortholog of murine KC and MIP-2), and TNF. Functional differences exist between human and murine resistin; yet given the aforementioned observations, we hypothesized that murine resistin promotes O3-induced lung pathology by inducing expression of the same inflammatory cytokines as human resistin. Consequently, we examined indexes of O3-induced lung pathology in wild-type and resistin-deficient mice following acute exposure to either filtered room air or O3. In wild-type mice, O3 increased bronchoalveolar lavage fluid (BALF) resistin. Furthermore, O3 increased lung tissue or BALF IL-1?, IL-6, KC, TNF, macrophages, neutrophils, and epithelial cells in wild-type and resistin-deficient mice. With the exception of KC, which was significantly greater in resistin-deficient compared with wild-type mice, no genotype-related differences in the other indexes existed following O3 exposure. O3 caused AHR to acetyl-?-methylcholine chloride (methacholine) in wild-type and resistin-deficient mice. However, genotype-related differences in airway responsiveness to methacholine were nonexistent subsequent to O3 exposure. Taken together, these data demonstrate that murine resistin is increased in the lungs of wild-type mice following acute O3 exposure but does not promote O3-induced lung pathology.

SUBMITTER: Razvi SS 

PROVIDER: S-EPMC4652149 | biostudies-literature | 2015 Nov

REPOSITORIES: biostudies-literature

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Resistin deficiency in mice has no effect on pulmonary responses induced by acute ozone exposure.

Razvi Shehla S SS   Richards Jeremy B JB   Malik Farhan F   Cromar Kevin R KR   Price Roger E RE   Bell Cynthia S CS   Weng Tingting T   Atkins Constance L CL   Spencer Chantal Y CY   Cockerill Katherine J KJ   Alexander Amy L AL   Blackburn Michael R MR   Alcorn Joseph L JL   Haque Ikram U IU   Johnston Richard A RA  

American journal of physiology. Lung cellular and molecular physiology 20150918 10


Acute exposure to ozone (O3), an air pollutant, causes pulmonary inflammation, airway epithelial desquamation, and airway hyperresponsiveness (AHR). Pro-inflammatory cytokines-including IL-6 and ligands of chemokine (C-X-C motif) receptor 2 [keratinocyte chemoattractant (KC) and macrophage inflammatory protein (MIP)-2], TNF receptor 1 and 2 (TNF), and type I IL-1 receptor (IL-1α and IL-1β)-promote these sequelae. Human resistin, a pleiotropic hormone and cytokine, induces expression of IL-1α, IL  ...[more]

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