1. Dexmedetomidine affects alveolar macrophage polarization through JAK2/STAT3 signaling pathway.
- Author
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GE Liang, LENG Yufang, ZHANG Peng, KONG Lingguo, and HAN Xudong
- Subjects
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JAK-STAT pathway , *GENE expression , *ALVEOLAR macrophages , *SPACE debris , *CELLULAR signal transduction - Abstract
Objective: To investigate the effect of dexmedetomidine (DEX) on the polarization of alveolar macrophages induced by lipopolysaccharide (LPS) and to explore the related mechanisms. Methods: Rat alveolar macrophages NR8383 were cultured in vitro. Experiment one was divided into control group, model group (1 μg/ml LPS), DEX low, medium and high dose groups (1, 5, 10 mg/kg DEX+10 mg/kg LPS). Experiment two was divided into DEX high dose group (10 mg/kg) and DEX high dose+Colivelin (JAK2/STAT3 signaling pathway activator) group (10 mg/kg DEX+0.5 μmol/L Colivelin). The morphological changes of rat alveolar macrophages NR8383 were observed by inverted microscope; RT-PCR method was used to detect the expression levels of iNOS and Arg1 mRNA in NR8383 cells, and flow cytometry was used to detect the expression levels of CD86 and CD163 proteins in NR8383 cells; Western blot was used to detect the expression levels of surface marker proteins TNF-α, iNOS, SOCS, Arg1, TGF-β and JAK2/ STAT3 signaling pathway related proteins in NR8383 cells. Results: Compared with control group, there were a lot of cell debris in the intercellular space of NR8383 in the model group, the proportions of iNOS mRNA, CD86 positive cells, and the expression levels of TNF-α, p-JAK2/JAK2, p-STAT3/STAT3 were significantly increased, the proportions of Arg1 mRNA, CD163 positive cells, and the expression levels of SOCS and TGF-β were significantly reduced (P<0.05); compared with the model group, the NR8383 intercellular cell debris in the DEX low, medium, and high dose groups were decreased, the proportions of iNOS mRNA, CD86 positive cells, and the expression levels of TNF-α, p-JAK2/JAK2, p-STAT3/STAT3 were significantly reduced, the proportions of Arg1 mRNA, CD163 positive cells, and the expression levels of SOCS and TGF- β were significantly increased (P<0.05). The reactivation of the JAK2/ STAT3 signal pathway by Colivelin could weaken the role of DEX in LPS induced NR8383 cell polarization. Conclusion: DEX can inhibit the M1 polarization of NR8383 cells induced by LPS, which may be achieved by inhibiting the JAK2/STAT3 signaling pathway. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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