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Mechanisms

Augmented angiogenic transcription factor, SOX18, is associated with asthma exacerbation

, BSORCID Icon, , PhDORCID Icon, , BSORCID Icon, , PhDORCID Icon & , MD, PhDORCID Icon
Pages 1143-1154 | Received 03 Jan 2020, Accepted 16 May 2020, Published online: 27 May 2020
 

Abstract

Background

Asthma characterized by airway hyperresponsiveness, inflammation, fibrosis, and angiogenesis. SRY-related HMG-box 18 (SOX18) is an important transcription factor involved in angiogenesis, tissue injury, wound-healing, and in embryonic cardiovascular and lymphatic vessels development. The role of angiogenic transcription factors, SOX18 and the related, prospero homeobox 1 (PROX1) and chicken ovalbumin upstream promoter transcription factor II (COUP-TFII), in asthma has had limited study.

Objective

In this study, we aimed to elucidate the role of SOX18 in the pathogenesis of bronchial asthma.

Methods

Plasma SOX18 protein was measured in control subjects, and subject with stable or exacerbated asthma. SOX18, PROX1, and COUP-TFII protein was measured by western blot, and immunohistochemistry in a murine model of ovalbumin-induced allergic asthma (OVA). SOX18, PROX1, and COUP-TFII protein was measured in lung human microvascular endothelial cells (HMVEC-L) and normal human bronchial epithelial (NHBE) cells treated with house dust mite (Der p1).

Results

Plasma SOX18 tended to be higher in subject with asthma compared to control subjects and increased more during exacerbation as compared to stable disease. In mice, OVA challenge lead to increased lung SOX18, PROX1, COUP-TFII, mucous gland hyperplasia and submucosal collagen. In NHBE cells, SOX18, PROX1 and COUP-TFII increased following Der p1 treatment. SOX18 protein increased in HMVEC-L following Der p1 treatment.

Conclusion

These results suggest that SOX18 may be involved in asthma pathogenesis and be associated with asthma exacerbation.

Declaration of interest

The authors declare that they have no competing interests.

Additional information

Funding

This research was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education (2017R1D1A1B03027822) and Soonchunhyang University (AS), and by the National Institutes of Health grants ES015675, HL077763, and HL085655 (GDL).

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