Soluble Interleukin-6 Receptor α Inhibits the Cytokine-Induced Fractalkine/CX3CL1 Expression in Human Vascular Endothelial Cells in Culture

2001 ◽  
Vol 269 (1) ◽  
pp. 35-41 ◽  
Author(s):  
Tomoh Matsumiya ◽  
Tadaatsu Imaizumi ◽  
Koji Fujimoto ◽  
Xuefan Cui ◽  
Takeo Shibata ◽  
...  
Keyword(s):  
Endothelial Cells ◽  
Interleukin 6 ◽  
Vascular Endothelial Cells ◽  
Vascular Endothelial ◽  
Cells In Culture ◽  
Interleukin 6 Receptor

scholarly journals Global Transcriptional Profiling Reveals Novel Autocrine Functions of Interleukin 6 in Human Vascular Endothelial Cells

2020 ◽  
Vol 2020 ◽  
pp. 1-12 ◽  
Author(s):  
Liza U. Ljungberg ◽  
Mulugeta M. Zegeye ◽  
Caroline Kardeby ◽  
Knut Fälker ◽  
Dirk Repsilber ◽  
...  
Keyword(s):  
Cell Cycle ◽  
Endothelial Cells ◽  
Pathway Analysis ◽  
Interleukin 6 ◽  
Vascular Endothelial Cells ◽  
Differential Regulation ◽  
Vascular Endothelial ◽  
Human Endothelial Cells ◽  
Cellular Functions ◽  
Cellular Movement

Background. Interleukin 6 (IL6) is a multifunctional cytokine produced by various cells, including vascular endothelial cells. IL6 has both pro- and non-/anti-inflammatory functions, and the response to IL6 is dependent on whether it acts via the membrane-bound IL6 receptor α (IL6Rα) (classic signaling) or the soluble form of the receptor (transsignaling). As human endothelial cells produce IL6 and at the same time express IL6Rα, we hypothesized that IL6 may have autocrine functions. Methods. Knockdown of IL6 in cultured human endothelial cells was performed using siRNA. Knockdown efficiency was evaluated using ELISA. RNA sequencing was employed to characterize the transcriptional consequence of IL6 knockdown, and Ingenuity Pathway Analysis was used to further explore the functional roles of IL6. Results. Knockdown of IL6 in cultured endothelial cells resulted in a 84-92% reduction in the release of IL6. Knockdown of IL6 resulted in dramatic changes in transcriptional pattern; knockdown of IL6 in the absence of soluble IL6Rα (sIL6Rα) led to differential regulation of 1915 genes, and knockdown of IL6 in the presence of sIL6Rα led to differential regulation of 1967 genes (fold change 1.5, false discovery rate<0.05). Pathway analysis revealed that the autocrine functions of IL6 in human endothelial cells are mainly related to basal cellular functions such as regulation of cell cycle, signaling, and cellular movement. Furthermore, we found that knockdown of IL6 activates functions related to adhesion, binding, and interaction of endothelial cells, which seem to be mediated mainly via STAT3. Conclusion. In this study, a large number of novel genes that are under autocrine regulation by IL6 in human endothelial cells were identified. Overall, our data indicate that IL6 acts in an autocrine manner to regulate basal cellular functions, such as cell cycle regulation, signaling, and cellular movement, and suggests that the autocrine functions of IL6 in human endothelial cells are mediated via IL6 classic signaling.

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