Suppr超能文献

培养的人青光眼小梁细胞细胞骨架的变化。

Cytoskeletal changes in cultured human glaucoma trabecular meshwork cells.

机构信息

Alcon Laboratories, Fort Worth, Texas, U.S.A.

出版信息

J Glaucoma. 1995 Jun;4(3):183-8.

Abstract

PURPOSE

Glucocorticoid treatment of cultured human trabecular meshwork (TM) cells has been shown to reorganize actin microfilaments into cross-linked actin networks (CLANs) and to alter TM cell function. The purpose of the present study is to determine whether similar microfilament structural changes occur in TM cells derived from glaucoma patients.

METHODS

The microfilament structures of nine different TM cell cultures, derived from four glaucoma patients and from five normal subjects, was examined by epifluorescent microscopy and by whole-mount transmission electron microscopy. The cells were cultured in the absence and presence of dexamethasone (DEX) for 7-14 days.

RESULTS

The normal TM cell lines and glaucoma cell line TM13 had relatively low levels of cross-linked actin networks in the absence of exogenously added glucocorticoids. In contrast, the glaucoma cell lines TM23, TM36C, and TM48D had high levels of CLANs without the addition of dexamethasone. The addition of 10 M DEX to the culture medium significantly increased CLAN expression in all normal as well as glaucoma TM cell lines.

CONCLUSION

CLAN formation in glaucoma TM cells or in TM cells exposed to glucocorticoids may be a factor contributing to the generation of ocular hypertension.

摘要

目的

已证实皮质类固醇处理培养的人眼小梁细胞(TM)可使细胞中的肌动蛋白微丝重组成交联肌动蛋白网络(CLANs)并改变 TM 细胞的功能。本研究旨在确定皮质类固醇是否会引起源自青光眼患者的 TM 细胞出现类似的微丝结构改变。

方法

通过相差荧光显微镜和全细胞透射电子显微镜观察 9 种不同 TM 细胞培养物(源自 4 名青光眼患者和 5 名正常受试者)的微丝结构。细胞在无或有地塞米松(DEX)的情况下培养 7-14 天。

结果

正常 TM 细胞系和青光眼细胞系 TM13 在没有外源性添加糖皮质激素的情况下,交联肌动蛋白网络的水平相对较低。相比之下,青光眼细胞系 TM23、TM36C 和 TM48D 在没有添加地塞米松的情况下具有高水平的 CLANs。在培养基中添加 10 μM DEX 可显著增加所有正常和青光眼 TM 细胞系中的 CLAN 表达。

结论

在青光眼 TM 细胞或暴露于皮质类固醇的 TM 细胞中形成 CLAN 可能是导致眼内压升高的一个因素。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验