Modulation of the lung inflammatory response to ozone by the estrous cycle

Physiol Rep. 2019 Mar;7(5):e14026. doi: 10.14814/phy2.14026.

Abstract

Emerging evidence suggests that sex differences exist in the control of lung innate immunity; however, the specific roles of sex hormones in the inflammatory response, and the mechanisms involved are unclear. Here, we investigated whether fluctuations in circulating hormone levels occurring in the mouse estrous cycle could affect the inflammatory response to air pollution exposure. For this, we exposed female mice (C57BL/6J, 8 weeks old) at different phases of the estrous cycle to 2 ppm of ozone or filtered air (FA) for 3 h. Following exposure, we collected lung tissue and bronchoalveolar lavage fluid (BAL), and performed lung function measurements to evaluate inflammatory responses and respiratory mechanics. We found a differential inflammatory response to ozone in females exposed in the luteal phase (metestrus, diestrus) versus the follicular phase (proestrus, estrus). Females exposed to ozone in the follicular phase had significantly higher expression of inflammatory genes, including Ccl2, Cxcl2, Ccl20, and Il6, compared to females exposed in the luteal phase (P < 0.05), and displayed differential activation of regulatory pathways. Exposure to ozone in the follicular phase also resulted in higher BAL neutrophilia, lipocalin levels, and airway resistance than exposure in the luteal phase (P < 0.05). Together, these results show that the effects of ozone exposure in the female lung are affected by the estrous cycle phase, and potentially hormonal status. Future studies investigating air pollution effects and inflammation in women should consider the menstrual cycle phase and/or circulating hormone levels.

Keywords: Air pollution; follicular phase; inflammation; luteal phase; sex hormones.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Video-Audio Media

MeSH terms

  • Airway Resistance / drug effects
  • Animals
  • Estradiol / blood
  • Estrous Cycle* / blood
  • Female
  • Gene Expression Regulation
  • Gene Regulatory Networks
  • Inflammation Mediators / metabolism*
  • Lung / drug effects*
  • Lung / metabolism
  • Lung / physiopathology
  • Luteinizing Hormone / blood
  • Mice, Inbred C57BL
  • Neutrophil Infiltration / drug effects
  • Ozone / toxicity*
  • Pneumonia / chemically induced*
  • Pneumonia / genetics
  • Pneumonia / metabolism
  • Pneumonia / physiopathology
  • Progesterone / blood
  • Respiratory Mechanics / drug effects
  • Transcriptome

Substances

  • Inflammation Mediators
  • Progesterone
  • Estradiol
  • Ozone
  • Luteinizing Hormone