Expression of sphingosine kinase 1 and sphingosine 1-phosphate receptor 3 in malaria-associated acute lung injury/acute respiratory distress syndrome in a mouse model

PLoS One. 2019 Sep 4;14(9):e0222098. doi: 10.1371/journal.pone.0222098. eCollection 2019.

Abstract

This study aimed to investigate the expression of sphingosine kinase 1 (SphK-1) and sphingosine 1-phosphate receptor 3 (S1PR-3) in a mouse model of malaria-associated acute lung injury/acute respiratory distress syndrome (ALI/ARDS). DBA/2 mice were infected with Plasmodium berghei ANKA to generate an experimental model of malaria-associated ALI/ARDS. The infected mice were divided into 2 groups based on the histopathological study of lung tissues: those with and those without ALI/ARDS. The expression of the SphK-1 and S1PR-3 proteins in the lung tissues was investigated using immunohistochemical staining and Western blot analysis. In addition, the S1P level was quantified in plasma and lung tissues using an enzyme-linked immunosorbent assay (ELISA). The results demonstrated that the cellular expression of the SphK-1 and S1PR-3 proteins was significantly upregulated in endothelial cells, alveolar epithelial cells and alveolar macrophages in the lung tissues of malaria-infected mice with ALI/ARDS compared with those in the control groups. The increased expression of the SphK-1 and S1PR-3 proteins was confirmed using Western blot analysis. The concentration of S1P in plasma and lung tissues was significantly decreased in malaria-infected mice with ALI/ARDS compared with non-ALI/ARDS and control mice. Furthermore, increased expression of the SphK-1 and S1PR-3 proteins significantly correlated with lung injury scores and S1P concentrations in malaria-infected mice with ALI/ARDS. These findings highlight increased expression of SphK-1 and S1PR-3 in the lung tissues of malaria-infected mice with ALI/ARDS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Lung Injury / complications
  • Acute Lung Injury / enzymology
  • Acute Lung Injury / metabolism*
  • Acute Lung Injury / pathology
  • Animals
  • Disease Models, Animal
  • Gene Expression Regulation, Enzymologic*
  • Lung / metabolism
  • Lung / pathology
  • Malaria / complications*
  • Male
  • Mice
  • Phosphotransferases (Alcohol Group Acceptor) / metabolism*
  • Respiratory Distress Syndrome / complications*
  • Respiratory Distress Syndrome / enzymology
  • Respiratory Distress Syndrome / metabolism*
  • Respiratory Distress Syndrome / pathology
  • Sphingosine-1-Phosphate Receptors / metabolism*

Substances

  • Sphingosine-1-Phosphate Receptors
  • Phosphotransferases (Alcohol Group Acceptor)
  • sphingosine kinase

Grants and funding

This work was supported by a research grant for new scholars to CP from the Thailand Research Fund (MRG5980054) and partially supported by the New Strategic Research (P2P) Project of Walailak University, Thailand (Contract number: CGS-P2P-2562-011).