Intrapulmonary airway smooth muscle is hyperreactive with a distinct proteome in asthma. Issue 1 (2nd July 2020)
- Record Type:
- Journal Article
- Title:
- Intrapulmonary airway smooth muscle is hyperreactive with a distinct proteome in asthma. Issue 1 (2nd July 2020)
- Main Title:
- Intrapulmonary airway smooth muscle is hyperreactive with a distinct proteome in asthma
- Authors:
- Ijpma, Gijs
Kachmar, Linda
Panariti, Alice
Matusovsky, Oleg S.
Torgerson, Dara
Benedetti, Andrea
Lauzon, Anne-Marie - Abstract:
- Constriction of airways during asthmatic exacerbation is the result of airway smooth muscle (ASM) contraction. Although it is generally accepted that ASM is hypercontractile in asthma, this has not been unambiguously demonstrated. Whether airway hyperresponsiveness (AHR) is the result of increased ASM mass alone or also increased contractile force generation per unit of muscle directly determines the potential avenues for treatment. To assess whether ASM is hypercontractile we performed a series of mechanics measurements on isolated ASM from intrapulmonary airways and trachealis from human lungs. We analysed the ASM and whole airway proteomes to verify if proteomic shifts contribute to changes in ASM properties. We report an increase in isolated ASM contractile stress and stiffness specific to asthmatic human intrapulmonary bronchi, the site of increased airway resistance in asthma. Other contractile parameters were not altered. Principal component analysis (PCA) of unbiased mass spectrometry data showed clear clustering of asthmatic subjects with respect to ASM specific proteins. The whole airway proteome showed upregulation of structural proteins. We did not find any evidence for a difference in the regulation of myosin activity in the asthmatic ASM. In conclusion, we showed that ASM is indeed hyperreactive at the level of intrapulmonary airways in asthma. We identified several proteins that are upregulated in asthma that could contribute to hyperreactivity. Our data alsoConstriction of airways during asthmatic exacerbation is the result of airway smooth muscle (ASM) contraction. Although it is generally accepted that ASM is hypercontractile in asthma, this has not been unambiguously demonstrated. Whether airway hyperresponsiveness (AHR) is the result of increased ASM mass alone or also increased contractile force generation per unit of muscle directly determines the potential avenues for treatment. To assess whether ASM is hypercontractile we performed a series of mechanics measurements on isolated ASM from intrapulmonary airways and trachealis from human lungs. We analysed the ASM and whole airway proteomes to verify if proteomic shifts contribute to changes in ASM properties. We report an increase in isolated ASM contractile stress and stiffness specific to asthmatic human intrapulmonary bronchi, the site of increased airway resistance in asthma. Other contractile parameters were not altered. Principal component analysis (PCA) of unbiased mass spectrometry data showed clear clustering of asthmatic subjects with respect to ASM specific proteins. The whole airway proteome showed upregulation of structural proteins. We did not find any evidence for a difference in the regulation of myosin activity in the asthmatic ASM. In conclusion, we showed that ASM is indeed hyperreactive at the level of intrapulmonary airways in asthma. We identified several proteins that are upregulated in asthma that could contribute to hyperreactivity. Our data also suggest enhanced force transmission associated with enrichment of structural proteins in the whole airway. These findings may lead to novel directions for treatment development in asthma. Intrapulmonary, but not tracheal, airway smooth muscle is hyperreactive in asthma, together with pro-contractile changes in the airway smooth muscle proteome. Several proteins were identified that could be targeted for treatment of the hyperreactivity. http://bit.ly/33esYSU … (more)
- Is Part Of:
- European respiratory journal. Volume 56:Issue 1(2020)
- Journal:
- European respiratory journal
- Issue:
- Volume 56:Issue 1(2020)
- Issue Display:
- Volume 56, Issue 1 (2020)
- Year:
- 2020
- Volume:
- 56
- Issue:
- 1
- Issue Sort Value:
- 2020-0056-0001-0000
- Page Start:
- Page End:
- Publication Date:
- 2020-07-02
- Subjects:
- Respiratory organs -- Diseases -- Periodicals
Respiration -- Periodicals
616.2 - Journal URLs:
- http://erj.ersjournals.com ↗
http://www.ersnet.org ↗
http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=mrj ↗
http://www.ingenta.com/journals/browse/ers/erj?mode=direct ↗ - DOI:
- 10.1183/13993003.02178-2019 ↗
- Languages:
- English
- ISSNs:
- 0903-1936
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library DSC - BLDSS-3PM
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