Volume 44 Issue 12
Dec.  2023
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Yidan FU, Wenting CHEN, Xiaoyang SU, Yan ZHAO, Danfeng LAN, Qiuping YANG. Role of Mertk-mediated NF-κb Pathway in Inflammatory Response of Schwann Cells[J]. Journal of Kunming Medical University, 2023, 44(12): 20-24. doi: 10.12259/j.issn.2095-610X.S20231203
Citation: Yidan FU, Wenting CHEN, Xiaoyang SU, Yan ZHAO, Danfeng LAN, Qiuping YANG. Role of Mertk-mediated NF-κb Pathway in Inflammatory Response of Schwann Cells[J]. Journal of Kunming Medical University, 2023, 44(12): 20-24. doi: 10.12259/j.issn.2095-610X.S20231203

Role of Mertk-mediated NF-κb Pathway in Inflammatory Response of Schwann Cells

doi: 10.12259/j.issn.2095-610X.S20231203
  • Received Date: 2023-09-28
    Available Online: 2023-12-20
  • Publish Date: 2023-12-25
  •   Objective  To explore the regulatory effect of Mertk expression level on NF-κb pathway in rat Schwann cells and its possible mechanism.   Methods  Rat Schwann cells were cultured in vitro, and the expression of Mertk in Schwann cells exposed to high glucose was detected by Western blot. Co-immunoprecipitation was used to detect the interaction between endogenous Mertk and Ikbkb. Western blot was used to detect the expression levels of Ikbkb, P65 and tumor necrosis factor-α in Schwann cells after Mertk silencing. The protein expressions of Mertk, Ikbkb and P65 after silencing Mertk were detected by immunofluorescence.   Results  Mertk was expressed in Schwann cells, and the expression level increased with the increase of glucose concentration. Co-immunoprecipitation assay showed that Mertk interacted with Ikbkb in rat Schwann cells. Compared with the control group, the expression level of Mertk was significantly decreased(P < 0.05), while Ikbkb, P65 and TNF-α were significantly increased(P < 0.05) after knock down expression of Mertk in Schwann cells. Immunofluorescence experiments showed that the fluorescence of Mertk was decreased, and the fluorescence of Ikbkb and P65 was increased in the silenced Schwann cells.  Conclusion  After the expression of Mertk is decreased, it can mediate the regulation of NF-κb pathway in Schwann cells through interaction with Ikbkb, and up-regulate the expression of P65 and inflammatory factor TNF-α.
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