Copyright
©The Author(s) 2025.
World J Diabetes. Mar 15, 2025; 16(3): 95092
Published online Mar 15, 2025. doi: 10.4239/wjd.v16.i3.95092
Published online Mar 15, 2025. doi: 10.4239/wjd.v16.i3.95092
Figure 7 Silencing of O-GlcNAc transferase inhibits M1 polarization and facilitates M2 polarization.
A: mRNA expression of inducible nitric oxide synthase and interleukin (IL)-6; B: IL-10 and arginase 1 in cells was measured using quantitative real-time polymerase chain reaction; C: Immunofluorescence staining was conducted to measure cluster of differentiation (CD) 86; D: CD206 levels. Scale bar: 50 μm; E: Relative fluorescence intensity of CD86 and CD206 was quantified; F and G: CD86 and CD206 levels were assessed and quantified by flow cytometry. aP < 0.05. 1P vs control. 2P vs lipopolysaccharide + high glucose + short hairpin RNA-negative control. LPS: Lipopolysaccharide; HG: High glucose; sh-NC: Short hairpin RNA-negative control; sh-OGT: Short hairpin RNA targeting O-GlcNAc transferase; iNOS: Inducible nitric oxide synthase; IL: Interleukin; CD: Cluster of differentiation; Arg1: Arginase 1; DAPI: 4’,6-Diamidino-2-phenylindole.
- Citation: Wu YK, Liu M, Zhou HL, He X, Wei J, Hua WH, Li HJ, Yuan QH, Xie YF. O-linked β-N-acetylglucosamine transferase regulates macrophage polarization in diabetic periodontitis: In vivo and in vitro study. World J Diabetes 2025; 16(3): 95092
- URL: https://www.wjgnet.com/1948-9358/full/v16/i3/95092.htm
- DOI: https://dx.doi.org/10.4239/wjd.v16.i3.95092