School of Medicine, Walailak University, Nakhon Si Thammarat, Thailand.
Tropical Medicine Research Unit, Research Institute for Health Sciences, Walailak University, Nakhon Si Thammarat, Thailand.
PLoS One. 2019 Sep 4;14(9):e0222098. doi: 10.1371/journal.pone.0222098. eCollection 2019.
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.
本研究旨在探讨神经酰胺激酶 1(SphK-1)和神经鞘氨醇 1-磷酸受体 3(S1PR-3)在疟疾相关急性肺损伤/急性呼吸窘迫综合征(ALI/ARDS)小鼠模型中的表达。用伯氏疟原虫 ANKA 感染 DBA/2 小鼠,生成疟疾相关 ALI/ARDS 的实验模型。根据肺组织的组织病理学研究,将感染的小鼠分为两组:有和没有 ALI/ARDS 的组。使用免疫组织化学染色和 Western blot 分析研究肺组织中 SphK-1 和 S1PR-3 蛋白的表达。此外,使用酶联免疫吸附测定(ELISA)定量血浆和肺组织中的 S1P 水平。结果表明,与对照组相比,ALI/ARDS 疟疾感染小鼠肺组织中内皮细胞、肺泡上皮细胞和肺泡巨噬细胞中 SphK-1 和 S1PR-3 蛋白的细胞表达显著上调。Western blot 分析证实了 SphK-1 和 S1PR-3 蛋白的表达增加。与非 ALI/ARDS 和对照组小鼠相比,ALI/ARDS 疟疾感染小鼠的血浆和肺组织中 S1P 浓度显著降低。此外,SphK-1 和 S1PR-3 蛋白的表达增加与疟疾感染小鼠的肺损伤评分和 S1P 浓度显著相关。这些发现突出了 SphK-1 和 S1PR-3 在疟疾感染伴有 ALI/ARDS 的小鼠肺组织中的表达增加。