Suppr超能文献

成纤维细胞生长因子10上调大鼠结膜上皮细胞中黏蛋白的表达。

Fibroblast growth factor 10 upregulates the expression of mucins in rat conjunctival epithelial cells.

作者信息

Ma Mingming, Zhang Zhengwei, Niu Weiran, Zheng Wenjing, Kelimu Jiang, Ke Bilian

机构信息

Department of Ophthalmology, Shanghai Key Laboratory of Fundus Diseases, First People's Hospital, Shanghai Jiao Tong University, Shanghai, China.

出版信息

Mol Vis. 2011;17:2789-97. Epub 2011 Oct 26.

Abstract

PURPOSE

This in vitro study aimed to gain insight into the function of fibroblast growth factor 10 (FGF10) on the ocular surface, especially its effect on mRNA expression of the mucins Muc1, Muc4, and Muc5ac, and mucin protein synthesis.

METHODS

We isolated primary cultured rat conjunctival epithelial cells (Cj-ECs) and treated them with FGF10 (1 ng/ml, 10 ng/ml, 100 ng/ml, and 200 ng/ml) and basic fibroblast growth factor 2 (FGF2; 10 ng/ml) for 24 h or 48 h. The proliferation of Cj-ECs was evaluated by 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium (MTS). mRNA levels of Muc1, Muc4, and Muc5ac were determined by real-time PCR. Synthesis levels of MUC1 and MUC4 were measured by western blot. Flow cytometry and Annexin V/PI double staining revealed degrees of apoptosis.

RESULTS

In primary culture, the epithelial cells were compact and cobblestone pavement in shape. Most of the cells were positive for cytokeratin (CK). FGF10 and FGF2 significantly stimulated Muc1, Muc4, and Muc5ac mRNA expression, cell proliferation, and synthesis of MUC1 and MUC4 proteins. FGF10 was more potent than FGF2 in these regards. FGF10 did not restrain the apoptosis of Cj-ECs.

CONCLUSIONS

The results of this study demonstrated that FGF10 is associated with the promotion of Cj-EC proliferation and mucin production. The effects of FGF10 on Cj-ECs support a rationale to investigate its therapeutic potential for ocular surface diseases.

摘要

目的

本体外研究旨在深入了解成纤维细胞生长因子10(FGF10)在眼表的功能,特别是其对黏蛋白Muc1、Muc4和Muc5ac的mRNA表达及黏蛋白蛋白质合成的影响。

方法

我们分离了原代培养的大鼠结膜上皮细胞(Cj - ECs),并用FGF10(1 ng/ml、10 ng/ml、100 ng/ml和200 ng/ml)和碱性成纤维细胞生长因子2(FGF2;10 ng/ml)处理24小时或48小时。通过3 -(4,5 - 二甲基噻唑 - 2 - 基)- 5 -(3 - 羧甲氧基苯基)- 2 -(4 - 磺基苯基)- 2H - 四唑(MTS)评估Cj - ECs的增殖。通过实时PCR测定Muc1、Muc4和Muc5ac的mRNA水平。通过蛋白质印迹法测量MUC1和MUC4的合成水平。流式细胞术和膜联蛋白V/碘化丙啶双重染色揭示细胞凋亡程度。

结果

在原代培养中,上皮细胞紧密且呈鹅卵石铺路状。大多数细胞细胞角蛋白(CK)呈阳性。FGF10和FGF2显著刺激Muc1、Muc4和Muc5ac的mRNA表达、细胞增殖以及MUC1和MUC4蛋白的合成。在这些方面,FGF10比FGF2更有效。FGF10并未抑制Cj - ECs的凋亡。

结论

本研究结果表明,FGF10与促进Cj - ECs增殖和黏蛋白产生有关。FGF10对Cj - ECs的作用为研究其在眼表疾病中的治疗潜力提供了理论依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a27/3209430/49a48f04d203/mv-v17-2789-f1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验