期刊
BRITISH JOURNAL OF OPHTHALMOLOGY
卷 88, 期 10, 页码 1343-1347出版社
BMJ PUBLISHING GROUP
DOI: 10.1136/bjo.2003.038133
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Aim: To examine the role of cytokine interleukin-1beta (IL-1beta) in retinal capillary cell death in diabetes. Methods: The effect of glucose on the expression of IL-1beta was measured in the bovine retinal endothelial cells. The role of IL-1beta in the accelerated endothelial cell loss was determined by investigating the effect of human recombinant IL-1beta on their apoptosis in normal and high glucose conditions, and was confirmed using interleukin-1 receptor antagonist (IL-1ra). Results: High glucose increased IL-1beta expression by 60% compared with cells incubated in 5 mM glucose ( p< 0.05). Incubation of cells with IL-1 beta increased NO levels by about 80% and activated NF-kappa B by 40%. In the same cells apoptosis was increased by 70% and caspase-3 activity was increased by 40%. Supplementation of IL-1 beta in 20 mM glucose medium further increased nitric oxide and NF-kappa B, and accelerated apoptosis, and addition of IL-1ra significantly decreased glucose induced abnormalities and apoptosis. Conclusions: IL-1 beta accelerates apoptosis of retinal capillary cells via activation of NF-kappa B, and the process is exacerbated in high glucose conditions. These studies suggest a possible role of IL-1 beta in the development of retinopathy in diabetes, and offer a possible rationale to test IL-1 beta receptor antagonists to inhibit the development of diabetic retinopathy.
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