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. Author manuscript; available in PMC: 2024 Mar 5.
Published in final edited form as: Int J Pharm. 2023 Feb 1;634:122661. doi: 10.1016/j.ijpharm.2023.122661

Table 1.

Characteristics of mucus in airway mucosal diseases

Airway mucus Mucus characteristics References
Healthy airway mucus
  • Normal mucin production from airway epithelium

  • Gel with deformable, elastic solid and viscous liquid

  • Contains 97% water and 2‒4% solid contents (mucins, salts, lipids, polypeptides, etc.)

  • Similar quantity of MUC5AC (proximal airways) and MUC5B (surface secretory cells) in airway mucus

(Fahy and Dickey, 2010; McGuckin et al., 2015; Rubin, 2007)
Asthma
  • Airway mucin stores increase due to goblet cell hypertrophy and hyperplasia

  • Surface epithelial mucous metaplasia and uncertain hyperplasia

  • Population of subepithelial bronchial microvessels increased but remodeling is not prominent

  • In severe disease conditions there is alteration in submucosal glands

  • Increased expression of MUC5AC and decreased expression of MUC5B gene

(Bonser et al., 2016; Bonser and Erle, 2017; Kuyper et al., 2003; Lachowicz-Scroggins et al., 2016)
Chronic obstructive pulmonary disease (COPD)
  • Increase in mucin stores

  • Surface epithelial mucous metaplasia and some hyperplasia

  • Volume/number of submucosal glands increase

  • Concentration of MUC5AC increases rather than MUC5B

(Anderson et al., 2015; Lin et al., 2020; Radicioni et al., 2021)
Cystic fibrosis (CF)
  • The levels of epithelial mucin stores are near normal

  • Submucosal glands are very prominent

  • More than 10% of solid content in mucus

  • Characterized by a predominant increase in MUC5B

(Button et al., 2016; Livraghi-Butrico et al., 2017; Martens et al., 2011)