Manipulation of dipeptidylpeptidase 10 in mouse and human in vivo and in vitro models indicates a protective role in asthma

• Published in: Disease models & mechanisms 2018-01, Vol.11 (1)
• Main Authors: Zhang, Youming, Poobalasingam, Thanushiyan, Yates, Laura L, Walker, Simone A, Taylor, Martin S, Chessum, Lauren, Harrison, Jackie, Tsaprouni, Loukia, Adcock, Ian M, Lloyd, Clare M, Cookson, William O, Moffatt, Miriam F, Dean, Charlotte H
• Format: Article
• Language: English
• Subjects: Airway resistance; Amino Acid Sequence; Animals; Archives & records; Asthma; Asthma - complications; Asthma - enzymology; Asthma - pathology; Asthma - prevention & control; Base Sequence; Cloning; Dipeptidyl-Peptidases and Tripeptidyl-Peptidases - chemistry; Dipeptidyl-Peptidases and Tripeptidyl-Peptidases - genetics; Dipeptidyl-Peptidases and Tripeptidyl-Peptidases - metabolism; Disease Models, Animal; DPP10; Epithelial Cells - metabolism; Ethylnitrosourea; Genetic testing; Genomes; Genotype; Homozygote; Humans; Hypersensitivity - complications; Hypersensitivity - pathology; IgE; In vitro fertilization; Inflammation - complications; Inflammation - pathology; Inflammation Mediators - metabolism; Localization; Lung - parasitology; Lung - pathology; Lungs; Mice; Mice, Mutant Strains; Mutation; Mutation - genetics; Point mutation; Proteins; Pyroglyphidae; Reproducibility of Results; Rodents; Sperm
• ISSN: 1754-8403; 1754-8411
• DOI: 10.1242/dmm.031369

We previously identified dipeptidylpeptidase 10 ( ) on chromosome 2 as a human asthma susceptibility gene, through positional cloning. Initial association results were confirmed in many subsequent association studies but the functional role of DPP10 in asthma remains unclear. Using the MRC Harwell N-ethyl-N-nitrosourea (ENU) DNA archive, we identified a point mutation in that caused an amino acid change from valine to aspartic acid in the β-propeller region of the protein. Mice carrying this point mutation were recovered and a congenic line was established ( ). Macroscopic examination and lung histology revealed no significant differences between wild-type and mice. However, after house dust mite (HDM) treatment, mutant mice showed significantly increased airway resistance in response to 100 mg/ml methacholine. Total serum IgE levels and bronchoalveolar lavage (BAL) eosinophil counts were significantly higher in homozygotes than in control mice after HDM treatment. DPP10 protein is present in airway epithelial cells and altered expression is observed in both tissue from asthmatic patients and in mice following HDM challenge. Moreover, knockdown of in human airway epithelial cells results in altered cytokine responses. These results show that a point mutation leads to increased airway responsiveness following allergen challenge and provide biological evidence to support previous findings from human genetic studies. This article has an associated First Person interview with the first author of the paper.