4.7 Article

α4β1 and αMβ2 Integrin Expression and Pro-Proliferative Properties of Eosinophil Subtypes in Asthma

期刊

JOURNAL OF PERSONALIZED MEDICINE
卷 11, 期 9, 页码 -

出版社

MDPI
DOI: 10.3390/jpm11090829

关键词

eosinophil subtypes; lung-resident eosinophils; inflammatory eosinophils; asthma; integrins; airway smooth muscle; apoptosis; proliferation

资金

  1. Research Council of Lithuania [S-MIP-19-24]
  2. Science Foundation of the Lithuanian University of Health Sciences

向作者/读者索取更多资源

Eosinophilic inflammation is a key feature of asthma, with distinct types of eosinophils influencing airway smooth muscle cell proliferation and viability through integrins. In asthma patients, exposure to specific allergens can enhance the pro-proliferative properties of inflammatory eosinophils, while resident eosinophils have a stronger effect on stimulating smooth muscle cell proliferation and viability.
Eosinophilic inflammation is one of the main pathophysiological features in asthma. Two subtypes of eosinophils exist in the lung and systemic circulation: lung-resident eosinophils (rEOS) and inflammatory eosinophils (iEOS). We evaluated the expression of alpha(4)beta(1) and alpha(M)beta(2) integrins of eosinophil subtypes and their influence on airway smooth muscle (ASM) cell proliferation and viability in asthma. We included 16 severe non-allergic eosinophilic asthma (SNEA) patients, 13 steroid-free, non-severe allergic asthma (AA) patients, and 12 healthy control subjects (HS). For AA patients, a bronchial allergen challenge with Dermatophagoides pteronyssinus was performed. The eosinophil subtypes were distinguished using magnetic bead-labeled antibodies against surface CD62L, and individual combined cell cultures were prepared with ASM cells. The integrins gene expression was analyzed by a quantitative real-time polymerase chain reaction. Proliferation was assessed by the Alamar blue assay, and viability by annexin V and propidium iodide staining. rEOS-like cells were characterized by the relatively higher gene expression of the beta(1) integrin subunit, whereas iEOS-like cells were characterized by the alpha(M) and beta(2) integrin subunits. The inclusion of either eosinophil subtypes in co-culture significantly increased the proliferation of ASM cells, and the effect of rEOS-like cells was stronger than iEOS-like cells (p < 0.05). Furthermore, rEOS-like cells had a more pronounced effect on reducing ASM cell apoptosis compared to that of iEOS-like cells (p < 0.05). Lastly, the bronchial allergen challenge significantly enhanced only the iEOS-like cells' effect on ASM cell proliferation and viability in AA patients (p < 0.05). These findings highlight the different expression of alpha(4)beta(1) and alpha(M)beta(2) integrins on distinct eosinophil subtypes in asthma. Therefore, rEOS-like cells have a stronger effect in stimulating ASM cell proliferation and viability; however, contact with specific allergens mainly enhances pro-proliferative iEOS-like cell properties.

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