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人视神经乳头星形胶质细胞作为内皮素-1的作用靶点

Human optic nerve head astrocytes as a target for endothelin-1.

作者信息

Prasanna Ganesh, Krishnamoorthy Raghu, Clark Abbot F, Wordinger Robert J, Yorio Thomas

机构信息

Department of Pharmacology and Neuroscience, Division of Cell Biology and Genetics, University of North Texas Health Science Center, Fort Worth, Texas 76107, USA.

出版信息

Invest Ophthalmol Vis Sci. 2002 Aug;43(8):2704-13.

Abstract

PURPOSE

To determine whether human optic nerve head astrocytes (hONAs) are target cells for the actions of endothelin (ET)-1, a potent vasoactive peptide, by causing astrocyte proliferation, as occurs in glaucomatous optic nerve heads. ET-1 levels are elevated in glaucomatous eyes, and administration of ET-1 to the retina causes glial activation and optic nerve damage in animal models in a manner similar to that observed in glaucoma.

METHODS

Well-characterized hONAs were used in this study. Cell proliferation of hONAs was assessed, after ET-1 treatment under serum-free culture conditions, with both a formazan assay and [3H]thymidine uptake. ET receptor involvement for cell proliferation was determined with BQ788 (an ETB antagonist), BQ610 (an ETA antagonist), PD142893 (an ET(A/B) mixed antagonist), and sarafotoxin 6C (S6C; an ET(B) agonist). ET-1-induced intracellular calcium ([Ca2+]i) in hONAs was measured by fura-2 imaging. RT-PCR was used to determine whether hONAs express mRNA for preproET-1, ET(A), and ET(B) receptors.

RESULTS

ET-1 (10 and 100 nM) caused a time-dependent proliferation of hONAs, which was completely blocked by PD142893, as detected by two different cell proliferation assays. The effects of ET-1 were blocked by BQ788 and were also mimicked by S6C, indicative of the involvement of ET(B) receptor activation. ET-1-induced elevation in [Ca2+]i, and cell proliferation were both blocked completely by the ET(A) antagonist BQ610, suggesting ET(A) receptor involvement. The hONAs expressed mRNA for ET(A) and ET(B) receptors as well as preproET-1, suggesting that these cells may also be a source for ET-1 in the optic nerve head.

CONCLUSIONS

ET-1 induces astroglial proliferation in cultured human optic nerve head astrocytes through ET(A/B) receptor activation. This is similar to the proliferation of ET-1 in brain astrocytes. These findings suggest that ET-1, which is elevated in glaucoma, could cause proliferation of ONAs in the optic nerve head.

摘要

目的

通过引发星形胶质细胞增殖,来确定人视神经乳头星形胶质细胞(hONAs)是否是强效血管活性肽内皮素(ET)-1作用的靶细胞,青光眼性视神经乳头中就会发生这种情况。青光眼患者眼中ET-1水平升高,在动物模型中,向视网膜注射ET-1会导致胶质细胞活化和视神经损伤,其方式与青光眼患者中观察到的相似。

方法

本研究使用了特征明确的hONAs。在无血清培养条件下用ET-1处理后,通过甲臜测定法和[3H]胸苷摄取来评估hONAs的细胞增殖。使用BQ788(一种ETB拮抗剂)、BQ610(一种ETA拮抗剂)、PD142893(一种ET(A/B)混合拮抗剂)和铃蟾毒素6C(S6C;一种ET(B)激动剂)来确定细胞增殖中ET受体的参与情况。通过fura-2成像测量ET-1诱导的hONAs细胞内钙([Ca2+]i)。RT-PCR用于确定hONAs是否表达前体ET-1、ETA和ETB受体的mRNA。

结果

ET-1(10和100 nM)导致hONAs呈时间依赖性增殖,通过两种不同的细胞增殖测定法检测发现,PD142893可完全阻断这种增殖。ET-1的作用被BQ788阻断,也被S6C模拟,这表明ET(B)受体激活参与其中。ET-1诱导的[Ca2+]i升高和细胞增殖均被ETA拮抗剂BQ610完全阻断,表明ETA受体也参与其中。hONAs表达ETA和ETB受体以及前体ET-1的mRNA,这表明这些细胞可能也是视神经乳头中ET-1的来源。

结论

ET-1通过激活ET(A/B)受体诱导培养的人视神经乳头星形胶质细胞增殖。这与ET-1在脑星形胶质细胞中的增殖情况相似。这些发现表明,青光眼患者中升高的ET-1可能导致视神经乳头中ONAs增殖。

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