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©The Author(s) 2025.
World J Diabetes. Aug 15, 2025; 16(8): 105228
Published online Aug 15, 2025. doi: 10.4239/wjd.v16.i8.105228
Published online Aug 15, 2025. doi: 10.4239/wjd.v16.i8.105228
Figure 1 Farnesoid X receptor positively regulates its expression by binding to the binding immunoglobulin protein promoter region.
A: Fluorescent enzyme reporter gene detection showed that the activity of the binding immunoglobulin protein (BiP) gene promoter increased in a dose-dependent manner after treatment with farnesoid X receptor agonist obeticholic acid (INT-747); B: After truncating the BiP gene promoter sequence, luciferase reporter gene detection showed that transcriptional activity was still present in the -376 to +200 sequence of the BiP gene promoter; C: Chromatin immunoprecipitation quantitative real time polymerase chain reaction results show that anti farnesoid X receptor antibodies significantly enrich the promoter sequence of BiP gene. aP < 0.05. bP < 0.01. cP < 0.001. dP < 0.0001. HG: High glucose; DMSO: Dimethyl sulfoxide; INT-747: Obeticholic acid; FXR: Farnesoid X receptor; Luc: Luciferase.
- Citation: Tang JY, Chong YJ, Yang L, Li X, Yang Y, Li JC, Mu J. Activation of farnesoid X receptor upregulates binding immunoglobulin protein expression and alleviates diabetic nephropathy. World J Diabetes 2025; 16(8): 105228
- URL: https://www.wjgnet.com/1948-9358/full/v16/i8/105228.htm
- DOI: https://dx.doi.org/10.4239/wjd.v16.i8.105228