Correlation of hyaluronan deposition with infiltration of eosinophils and lymphocytes in a cockroach-induced murine model of asthma

Glycobiology. 2013 Jan;23(1):43-58. doi: 10.1093/glycob/cws122. Epub 2012 Aug 23.

Abstract

Asthma is a chronic inflammatory disease that exhibits airway remodeling with changes in the extracellular matrix (ECM). The role of the ECM in mediating these changes is poorly understood. Hyaluronan (HA), a major component of the ECM, has been implicated in many biological processes in diseases. This study investigates the processes involved in HA synthesis, deposition and localization during the propagation of cockroach-induced asthma. Mice were sensitized and challenged with cockroach antigen, and sacrificed at various time points during an 8-week challenge protocol. Analysis of bronchoalveolar lavage (BAL) fluid revealed an increase in total nucleated cells as early as 6h, which peaked at 6 days. Histopathologic analysis of the lung tissue revealed an influx of inflammatory cells at the peribronchial and perivascular regions starting at 12 h, which peaked at 6 days and persisted to 8 weeks. Eosinophils predominated in the early time points while lymphocytes predominated during the late time points. Quantitative polymerase chain reaction (PCR) data showed that hyaluronan synthase 1 (HAS1) mRNA peaked within 6 h and then declined. HAS2 mRNA also peaked within 6 h but remained elevated throughout the 8-week exposure course. HA levels in lung tissue and BAL increased at 12 h and peaked by 6 and 8 days, respectively. Inflammatory cells and new collagen formation localized in areas of HA deposition. Taken together, these data support a role for HA in the pathogenesis in asthma.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Allergens / immunology
  • Animals
  • Asthma / immunology*
  • Asthma / pathology
  • Bronchoalveolar Lavage Fluid / cytology
  • Cockroaches / immunology
  • Disease Models, Animal
  • Eosinophils / immunology*
  • Eosinophils / pathology
  • Extracellular Matrix / metabolism
  • Female
  • Glucuronosyltransferase / genetics
  • Glucuronosyltransferase / metabolism
  • Hyaluronan Synthases
  • Hyaluronic Acid / immunology*
  • Lung / immunology
  • Lung / pathology
  • Lymphocytes / immunology*
  • Lymphocytes / pathology
  • Mice
  • Mice, Inbred BALB C

Substances

  • Allergens
  • Hyaluronic Acid
  • Glucuronosyltransferase
  • Has2 protein, mouse
  • Hyaluronan Synthases