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雌激素对永生化和原代人角膜上皮细胞培养物中基质金属蛋白酶和细胞因子的比较作用。

Comparative effects of estrogen on matrix metalloproteinases and cytokines in immortalized and primary human corneal epithelial cell cultures.

作者信息

Suzuki Tomo, Sullivan David A

机构信息

Schepens Eye Research Institute and Department of Ophthalmology, Harvard Medical School, Boston, MA 02114, USA.

出版信息

Cornea. 2006 May;25(4):454-9. doi: 10.1097/01.ico.0000220777.70981.46.

Abstract

PURPOSE

Recently, we found that 17beta-estradiol induces cytokine and MMP gene expression in SV40 immortalized human corneal epithelial cells (SV40 HCEs). The purpose of this study was to determine if 17beta-estradiol stimulates MMP secretion by cultures of SV40 HCEs and primary human corneal epithelial cells. Further, we determined if estrogen influenced cytokine and MMP gene expression in the primary cultures.

METHODS

Gelatin zymography was used to identify MMP-2 and MMP-9 gelatinase activity in the culture medium from SV40 HCEs and primary human corneal epithelial cell cultures exposed to vehicle or 17beta-estradiol for 6 or 24 hour. In addition, 17beta-estradiol effects on cytokine and MMP gene expression in primary cultures were evaluated by real-time PCR methods.

RESULTS

17beta-estradiol had no significant effects on MMP activity in the culture media of either SV40 HCEs or primary corneal epithelial cell cultures. SV40 HCEs secreted predominantly MMP-2, whereas the primary cultures secreted predominantly MMP-9. In primary cultures, 17beta-estradiol caused a significant decrease of IL-6 and IL-8 gene expression, but had no effect on the levels of IL-1beta, MMP-2, and MMP-9 gene expression.

CONCLUSIONS

Our findings suggest that 17beta-estradiol effects on gelatinase gene expression in SV40 HCEs are not translated into changes in secreted MMP activity. Estrogen influences on gene expression of cytokine and MMPs in primary cultures are different from those in SV40 HCEs.

摘要

目的

最近,我们发现17β-雌二醇可诱导SV40永生化人角膜上皮细胞(SV40 HCEs)中细胞因子和基质金属蛋白酶(MMP)基因的表达。本研究的目的是确定17β-雌二醇是否能刺激SV40 HCEs和原代人角膜上皮细胞培养物中MMP的分泌。此外,我们还确定了雌激素是否会影响原代培养物中细胞因子和MMP基因的表达。

方法

采用明胶酶谱法鉴定暴露于溶剂或17β-雌二醇6小时或24小时后的SV40 HCEs和原代人角膜上皮细胞培养物培养基中MMP-2和MMP-9明胶酶活性。此外,通过实时PCR方法评估17β-雌二醇对原代培养物中细胞因子和MMP基因表达的影响。

结果

17β-雌二醇对SV40 HCEs或原代角膜上皮细胞培养物培养基中的MMP活性无显著影响。SV40 HCEs主要分泌MMP-2,而原代培养物主要分泌MMP-9。在原代培养物中,17β-雌二醇导致IL-6和IL-8基因表达显著降低,但对IL-1β、MMP-2和MMP-9基因表达水平无影响。

结论

我们的研究结果表明,17β-雌二醇对SV40 HCEs中明胶酶基因表达的影响并未转化为分泌型MMP活性的变化。雌激素对原代培养物中细胞因子和MMPs基因表达的影响与SV40 HCEs中的不同。

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