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Endogenous Chemerin Limits the Severity of Ozone-Induced Airway Hyperresponsiveness Irrespective of Body Mass

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  • Personal Author:
  • Description:
    Rationale: Tumor necrosis factor-a, a pleiotropic adipocytokine, limits the severity of airway hyperresponsiveness (AHR), a cardinal feature of asthma, in obese mice exposed to ozone (O3), a criteria pollutant and non-atopic asthma stimulus. However, in this phenomenon, the contribution of chemerin, an adipocytokine and non-chemokine chemoattractant for natural killer cells, macrophages and plasmacytoid dendritic cells, is unknown. Consequently, our goal was to asseverate the relevance of chemerin in the development of O3-induced AHR in obesity. Methods: Wild-type C57BL/6J mice and mice genetically deficient in chemerin (chemerin-deficient mice) were fed standard chow or a diet consisting of 60 kcal % fat (high-fat diet; HFD) from weaning until 30 weeks of age. At 30 weeks of age, mice were exposed to either filtered room air (air) or O3 (2 ppm) for three hours. Twenty-four hours following cessation of exposure, indices of airway responsiveness to methacholine [airway resistance and coefficients of lung tissue damping and elastance] were measured using the forced oscillation technique. Results: Consumption of a HFD by wild-type and chemerin-deficient mice led to obesity. Following air exposure, airway responsiveness to methacholine was greater in chemerin-deficient as compared to wild-type mice irrespective of the diet consumed. All mice exposed to O3 exhibited AHR. Nevertheless, regardless of the diet consumed, airway responsiveness was greater in chemerin-deficient as compared to wild-type mice following O3 exposure. Conclusions: Chemerin limits the severity of airway responsiveness in the presence and absence of inciting stimuli and may be a therapeutic target to limit exaggerated airway narrowing observed in obese and non-obese asthmatics. [Description provided by NIOSH]
  • Subjects:
  • Keywords:
  • ISSN:
    0091-6749
  • Document Type:
  • Genre:
  • Place as Subject:
  • CIO:
  • Division:
  • Topic:
  • Location:
  • Volume:
    153
  • Issue:
    2
  • NIOSHTIC Number:
    nn:20070243
  • Citation:
    J Allergy Clin Immunol 2024 Feb; 153(2)(Suppl):AB256
  • CAS Registry Number:
  • Federal Fiscal Year:
    2024
  • Peer Reviewed:
    False
  • Source Full Name:
    Journal of Allergy and Clinical Immunology
  • Supplement:
    Suppl
  • Collection(s):
  • Main Document Checksum:
    urn:sha-512:1f52101187504f6fbbd0cf13032a8987c2b40dbf92daa2d3b1140a4077ed152db6533239b957cbd2da3ce0a88b35443b9e660235c0f6068e503caeb03bcbdf37
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  • File Type:
    Filetype[PDF - 125.81 KB ]
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