Endothelial Semaphorin 7A Promotes Inflammation in Seawater Aspiration-Induced Acute Lung Injury

International Journal of Molecular Sciences

Minlong Zhang¹  Li Wang¹  Mingqing Dong²  Zhichao Li²  Faguang Jin¹ 

[1] Department of Respiration, Tangdu Hospital, Fourth Military Medical University, Xi’an 710038, China; E-Mails:;Department of Pathology and Pathophysiology, Fourth Military Medical University, Xi’an 710032, China; E-Mail:

关键词: Semaphorin 7A;    acute lung injury;    seawater;   

DOI  :  10.3390/ijms151119650

来源: mdpi

【 摘 要 】

Inflammation is involved in the pathogenesis of seawater aspiration-induced acute lung injury (ALI). Although several studies have shown that Semaphorin 7A (SEMA7A) promotes inflammation, there are limited reports regarding immunological function of SEMA7A in seawater aspiration-induced ALI. Therefore, we investigated the role of SEMA7A during seawater aspiration-induced ALI. Male Sprague–Dawley rats were underwent seawater instillation. Then, lung samples were collected at an indicated time for analysis. In addition, rat pulmonary microvascular endothelial cells (RPMVECs) were cultured and then stimulated with 25% seawater for indicated time point. After these treatments, cells samples were collected for analysis. In vivo, seawater instillation induced lung histopathologic changes, pro-inflammation cytokines release and increased expression of SEMA7A. In vitro, seawater stimulation led to pro-inflammation cytokine release, cytoskeleton remodeling and increased monolayer permeability in pulmonary microvascular endothelial cells. In addition, knockdown of hypoxia-inducible factor (HIF)-1α inhibited the seawater induced increase expression of SEMA7A. Meanwhile, knockdown of SEMA7A by specific siRNA inhibited the seawater induced aberrant inflammation, endothelial cytoskeleton remodeling and endothelial permeability. These results suggest that SEMA7A is critical in the development of lung inflammation and pulmonary edema in seawater aspiration-induced ALI, and may be a therapeutic target for this disease.

【 授权许可】

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© 2014 by the authors; licensee MDPI, Basel, Switzerland.