Publications by authors named "Shu-Hua Fu"

Diabetic retinopathy (DR) is one of the most common complications of diabetes worldwide and is associated with visual loss and blindness. However, effective treatments for both early- and late-stage DR remain lacking. A streptozotocin-induced diabetic mouse model and high glucose (HG)-treated Müller cell model were established.

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The dysregulated microRNAs (miRNAs) are involved in diabetic retinopathy progression. Epithelial mesenchymal transition (EMT) and cell permeability are important events in diabetic retinopathy. However, the function and mechanism of miR-195 in EMT and cell permeability in diabetic retinopathy remain largely unclear.

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This study investigated the effects and mechanisms of miR-132 related to the permeability and mobility of human retinal pigment epithelium ARPE-19 cells in high-glucose (HG) condition. ARPE-19 cells were cultured in normal and HG condition and identified by immunofluorescence staining. Cell viability was assessed by the MTT assay, cell permeability was assessed by the FITC-dextran assay and cell mobility was assessed by the wound healing assay.

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Objective: To investigate the dry eye symptoms after cataract surgery in MGD patients and their relationships METHODS: The study included 115 patients (115 eyes) with age-related cataract that underwent uncomplicated cataract surgery, and the patients were divided into two groups according to the MGD diagnostic criteria: group A (MGD group) and group B (control group). Schirmer I test (ST-I), tear breakup time (TBUT), and corneal fluorescein staining (CFS) were performed preoperatively and at 3 days, 7 days, 14 days, and 30 days postoperatively. We also measured eyelid meibomian gland morphology, meibomian gland expression, and meibum character scores before and after the cataract surgery.

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Retinal injury plays a leading role in the onset of visual impairment. Current forms of treatment are not able to ameliorate scarring, cell death and tissue and axon regeneration. Recently, microRNA-216a (miR-216a) has been reported to regulate snx5, a novel notch signalling pathway component during retinal development.

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Article Synopsis
  • Diabetic retinopathy is linked to increased cell permeability and epithelial-mesenchymal transition (EMT), prompting researchers to explore the mechanisms behind this effect in retinal pigment epithelial (RPE) cells under high glucose conditions.
  • The study utilized specific shRNAs to knock down proteins like ARF6, GEP100, and VEGFR2, measuring cell migration and protein levels, which showed that high glucose led to heightened cell migration, permeability, EMT, and VEGF expression in RPE cells.
  • Knockdown of VEGFR2 was found to counteract the effects of high glucose on RPE cells by disrupting the ARF6 and MAPK pathways, while knocking down ARF6 or GEP100 also inhibited these
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