Abstract

Inhaled drugs are critical for the treatment of inflammatory airway diseases such as chronic obstructive pulmonary disease (COPD). To develop better therapeutics for pulmonary disease it is of potential importance to understand molecular mechanisms of local biotransformation in the lung. Alveolar epithelial type II (ATII) cells have a key role in homeostasis in the lung, but little is known about expression patterns of genes encoding cytochrome P450 (CYP) enzymes in ATII cells. In addition, alteration of CYP gene expression has not been fully defined in COPD. We previously established a method to purify ATII cells from the adult human lung using fluorescence‐activated cell sorting. By employing this technique we determined gene expression patterns of 14 CYP enzymes in ATII cells from nonsmokers (n = 4) and smokers (n = 4), both having normal pulmonary function. Although most CYP genes are highly expressed in primary hepatocytes, we found that CYP1B1 mRNA expression was 7.2‐fold higher in ATII compared to hepatocytes (P = .0275). Additionally we noted a 3.0‐fold upregulation of CYP2C19 and 50% reduction in CYP2J2 mRNA expressions in ATII cells isolated from patients with COPD (n = 3) compared to smokers without COPD (n = 4). These data, for the first time, detail a comprehensive set of genes encoding CYP enzymes in human ATII cells and highlights differentially expressed CYP mRNAs of patients with COPD. Such understanding may have important implications for the development of novel inhaled drugs.

Highlights

  • Among 14 cytochrome P450 (CYP) genes tested, CYP1A2 and CYP3A4 mRNAs were not detected in the isolated Alveolar epithelial type II (ATII) cells

  • In the remaining 12 CYP genes only CYP1B1 mRNA significantly increased in ATII cells compared to hepatocytes (Figure 1)

  • Considering recent studies using rat ATII cells indicated that proinflammatory cytokines such as tumor necrosis factor-a augmented genotoxic effects of polycyclic aromatic hydrocarbon (PAH) through CYP1B1,17,18 our results give extra weight and importance to the role of such a mechanism in the development of lung carcinoma under proinflammatory conditions

Read more

Summary

Introduction

CYP1B1 metabolically activates polycyclic aromatic hydrocarbons (PAHs) such as Benzo[a]pyrene contained in tobacco smoke to generate mutagenic and carcinogenic compounds.[16] Considering recent studies using rat ATII cells indicated that proinflammatory cytokines such as tumor necrosis factor-a augmented genotoxic effects of PAHs through CYP1B1,17,18 our results give extra weight and importance to the role of such a mechanism in the development of lung carcinoma under proinflammatory conditions.

Objectives
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call