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交感神经支配调节大鼠视网膜的基底膜增厚和周细胞数量。

Sympathetic innervation regulates basement membrane thickening and pericyte number in rat retina.

作者信息

Wiley Luke A, Rupp Gerald R, Steinle Jena J

机构信息

Department of Physiology, Southern Illinois University School of Medicine, Carbondale, Illinois 62901, USA.

出版信息

Invest Ophthalmol Vis Sci. 2005 Feb;46(2):744-8. doi: 10.1167/iovs.04-1023.

Abstract

PURPOSE

To determine whether loss of sympathetic innervation alters basement membrane thickness and pericyte loss.

METHODS

Sympathetic innervation to the eye was destroyed by surgical removal of the right superior cervical ganglion in rats. Basement membrane changes were assessed by real-time PCR and electron microscopy. The number of pericytes was measured by immunofluorescent staining for NG2 proteoglycan. Steady-state mRNA levels were also evaluated for platelet-derived growth factor-BB (PDGF-BB).

RESULTS

Loss of sympathetic innervation caused a significant increase in steady state mRNA levels of fibronectin and a 15% increase in laminin-beta 1 mRNA 3 weeks after surgical sympathectomy. Protein expression also increased at this point. In addition, capillary basement membrane thickness increased significantly. NG2 proteoglycan staining decreased significantly in pericytes in the sympathectomized rat retina. Steady state mRNA for PDGF-BB decreased significantly 6 weeks after surgery.

CONCLUSIONS

Sympathetic nerves may be compromised in diabetes, and these findings suggest that they may regulate some complications of diabetic retinopathy. Gene expression levels of fibronectin and laminin-beta 1 changed between 1 and 3 weeks. These data are supported by electron microscopy, which showed the increase in basement membrane thickness in vivo. Loss of sympathetic innervation to the eye also caused a decrease in the number of pericytes. Steady state mRNA expression of PDGF-BB was reduced, suggesting a mechanism for the loss of pericytes in the sympathectomized retina. Overall, these results suggest that sympathetic nerve alterations may function in some complications observed in diabetic retinopathy, and this may be a suitable model to investigate therapies for this disorder.

摘要

目的

确定交感神经去神经支配是否会改变基底膜厚度和周细胞丢失情况。

方法

通过手术切除大鼠右侧颈上神经节来破坏眼部的交感神经支配。通过实时聚合酶链反应和电子显微镜评估基底膜变化。通过对NG2蛋白聚糖进行免疫荧光染色来测量周细胞数量。还评估了血小板衍生生长因子-BB(PDGF-BB)的稳态mRNA水平。

结果

交感神经去神经支配导致在手术交感神经切除术后3周,纤连蛋白的稳态mRNA水平显著增加,层粘连蛋白-β1 mRNA增加15%。此时蛋白质表达也增加。此外,毛细血管基底膜厚度显著增加。在去交感神经支配的大鼠视网膜中,周细胞的NG2蛋白聚糖染色显著减少。手术后6周,PDGF-BB的稳态mRNA显著降低。

结论

糖尿病患者的交感神经可能受损,这些发现表明它们可能调节糖尿病视网膜病变的一些并发症。纤连蛋白和层粘连蛋白-β1的基因表达水平在1至3周之间发生变化。电子显微镜证实了这些数据,其显示体内基底膜厚度增加。眼部交感神经去神经支配也导致周细胞数量减少。PDGF-BB的稳态mRNA表达降低,提示去交感神经支配视网膜中周细胞丢失的机制。总体而言,这些结果表明交感神经改变可能在糖尿病视网膜病变中观察到的一些并发症中起作用,这可能是研究该疾病治疗方法的合适模型。

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