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©The Author(s) 2025.
World J Diabetes. Mar 15, 2025; 16(3): 92003
Published online Mar 15, 2025. doi: 10.4239/wjd.v16.i3.92003
Published online Mar 15, 2025. doi: 10.4239/wjd.v16.i3.92003
Figure 1 Differential expression of lnc-MGC and miR-495-3p in the diabetic retinopathy rat retina and cell model.
A: Detection of lnc-MGC and miR-495-3p expression in diabetic retinopathy rat retina tissue by RT-qPCR; B: Expression levels of lnc-MGC and miR-495-3p in the cell model were detected by RT-qPCR; C: Localization of lnc-MGC in ARPE-19 cells was detected by fluorescence in situ hybridization (FISH). The scale bar represents 10 μm; D: Localization of miR-495-3p in ARPE-19 cells was detected by FISH. The scale bar represents 10 μm. aP < 0.001. NC: Normal control; DR: Diabetic retinopathy; HG: High glucose.
- Citation: Luo YY, Ba XY, Wang L, Zhang YP, Xu H, Chen PQ, Zhang LB, Han J, Luo H. LEF1 influences diabetic retinopathy and retinal pigment epithelial cell ferroptosis via the miR-495-3p/GRP78 axis through lnc-MGC. World J Diabetes 2025; 16(3): 92003
- URL: https://www.wjgnet.com/1948-9358/full/v16/i3/92003.htm
- DOI: https://dx.doi.org/10.4239/wjd.v16.i3.92003