Adenovirus vector-mediated YKL-40 shRNA attenuates eosinophil airway inflammation in a murine asthmatic model
Autor: | Suqin Ben, Aying Ma, Danruo Fang, Ling Wang, Yi Wu, Aihua Bao, Ying Zheng, Huanxia Shang |
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Rok vydání: | 2020 |
Předmět: |
musculoskeletal diseases
0301 basic medicine Eotaxin Chemokine Ovalbumin Inflammation Biology Adenoviridae Small hairpin RNA Mice 03 medical and health sciences 0302 clinical medicine Gene expression Genetics medicine Animals Chitinase-3-Like Protein 1 RNA Small Interfering Lung Molecular Biology Mice Inbred BALB C medicine.diagnostic_test respiratory system Eosinophil Mucus Asthma respiratory tract diseases Eosinophils Disease Models Animal 030104 developmental biology Bronchoalveolar lavage medicine.anatomical_structure 030220 oncology & carcinogenesis Immunology biology.protein Molecular Medicine medicine.symptom |
Zdroj: | Gene Therapy. 28:177-185 |
ISSN: | 1476-5462 0969-7128 |
DOI: | 10.1038/s41434-020-00202-0 |
Popis: | Recent studies have revealed that YKL-40 is involved in the pathogenesis of asthma. However, its specific mechanism remains unclear. The present study aims to investigate the effect of adenovirus vector-mediated YKL-40 short hairpin RNA (shRNA) on regulation of airway inflammation in a murine asthmatic model. Mice were assessed for airway hyperresponsiveness (AHR), total leukocytes and the percentage of eosinophil cells in bronchoalveolar lavage fluid (BALF). YKL-40 mRNA and protein expression levels were detected using quantitative real-time PCR and western blot assays. Enzyme-linked immunosorbent assay (ELISA) was used to detect YKL-40 and eosinophil-related chemokine expression levels in BALF and serum. Lung histology analyses were performed to evaluate the degree of inflammatory cell infiltration around the airway and airway mucus secretion.YKL-40 shRNA significantly inhibited the YKL-40 gene expression in asthmatic mice. In addition, YKL-40 shRNA alleviated eosinophilic airway inflammation, AHR, airway mucus secretion and decreased the levels of YKL-40 in BALF and serum in a murine asthmatic model. The levels and mRNA expression of IL-5, IL-13 in asthmatic mice lung tissues, eotaxin, and GM-CSF in BALF and serum significantly decreased. Bone marrow signaling molecules including IL-5, eotaxin, and GM-CSF were correlated with decreased levels of YKL-40. The study reveals that YKL-40 could be involved in asthma inflammation by altering bone marrow signaling molecules. YKL-40 gene RNA interference could provide new therapeutic strategies for asthma. |
Databáze: | OpenAIRE |
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