Gene expression and immunolocalization of 15-lipoxygenase isozymes in the airway mucosa of smokers with chronic bronchitis
| Autor: | Keith Hattotuwa, Wai L. Liu, Michael Yeadon, Will Elston, Johan Kips, Neil Barnes, Peter K. Jeffery, Elizabeth Gamble, Jie Zhu, Virginia De Rose, A Oliva, Iain Kilty, Romain Pauwels, Yu Sheng Qiu, Helen Granger, Stephen Jenkinson |
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| Rok vydání: | 2002 |
| Předmět: |
Pulmonary and Respiratory Medicine
Adult Male Chronic bronchitis Pathology medicine.medical_specialty Biopsy Clinical Biochemistry In situ hybridization Respiratory Mucosa airway inflammation Gene Expression Regulation Enzymologic Downregulation and upregulation 15-lipoxygenase chronic bronchitis Gene expression medicine Arachidonate 15-Lipoxygenase Humans RNA Messenger Molecular Biology Aged Submucosal glands medicine.diagnostic_test Chemistry Reverse Transcriptase Polymerase Chain Reaction Smoking Interleukin Cell Biology Middle Aged Molecular biology Bronchitis Chronic Isoenzymes Immunohistochemistry Female |
| Zdroj: | American journal of respiratory cell and molecular biology. 27(6) |
| ISSN: | 1044-1549 |
| Popis: | 15-lipoxygenase (15-LO) has been implicated in the inflammation of chronic bronchitis (CB), but it is unclear which of its isoforms, 15-LOa or 15-LOb, is primarily involved. To detect 15-LO gene (mRNA) and protein expression, we have applied in situ hybridization (ISH) and immunohistochemistry (IHC), respectively, to bronchial biopsies obtained from 7 healthy nonsmokers (HNS), 5 healthy smokers (HS), and 8 smokers with CB, and additionally include the airways of lungs resected from 11 asymptomatic smokers (AS) and 11 smokers with CB. Compared with HNS, biopsies in CB demonstrated increased numbers of 15-LOa mRNA+ cells (median: HNS = 31.3/mm(2) versus CB = 84.9/mm(2), P < 0.01) and protein+ cells (HNS = 2.9/mm(2) versus CB = 32.1/mm(2), P < 0.01). The HS group also showed a significant increase in protein+ cells (HNS = 2.9/mm(2) versus HS = 14/mm(2), P < 0.05). In the resected airways, 15-LOa protein+ cells in the submucosal glands of the CB group were more numerous than in the AS group (AS = 33/mm(2) versus CB = 208/mm(2); P < 0.001). 15-LOa mRNA+ and protein+ cells consistently outnumbered 15-LOb by approximately 7- and 5-fold, respectively (P < 0.01). Quantitative reverse transcriptase polymerase chain reaction of complementary biopsies confirmed the increased levels of 15-LOa in CB compared with that in either HNS or HS (P < 0.05). There was no difference between the subject groups with respect to 15-LOb expression. The numbers of cells expressing mRNA for 15-LOa in CB showed a positive association with those expressing interleukin (IL)-4 mRNA (r = 0.80; P < 0.01). We conclude that the upregulation of 15-LO activity in the airways of HS and of smokers with CB primarily involves the 15-LOa isoform: the functional consequences of its association the upregulation of IL-4 in chronic bronchitis requires further study. |
| Databáze: | OpenAIRE |
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