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紫外线对犬角膜中基质金属蛋白酶的调节作用。

Modulation of matrix metalloproteinases by ultraviolet radiation in the canine cornea.

作者信息

Chandler Heather L, Kusewitt Donna F, Colitz Carmen M H

机构信息

Department of Veterinary Biosciences, College of Veterinary Medicine, The Ohio State University, 1900 Coffey Road, Columbus, OH 43201, USA.

出版信息

Vet Ophthalmol. 2008 May-Jun;11(3):135-44. doi: 10.1111/j.1463-5224.2008.00575.x.

Abstract

PURPOSE

To determine whether ultraviolet (UV) radiation can modulate expression and regulation of matrix metalloproteinases (MMP) in the canine cornea and to examine the expression of MMPs in canine chronic superficial keratitis (CSK).

METHODS

Immunohistochemistry for MMP-2 and MMP-9 was performed on samples of CSK. In vitro, canine corneal epithelial cell (CEC) and stromal cell cultures were exposed to UV-irradiation. Following 2, 8 or 24 h, cells were harvested. MMP expression was examined by zymography, and RT-PCR was used to examine expression of Slug and Snail. CEC cultures treated with an EGFR inhibitor or a p38 inhibitor were UV-exposed and harvested 24 h later to examine expression of MMPs, Slug and Snail.

RESULTS

Canine CSK had increased immunopositivity for both MMP-2 and MMP-9 compared to normal canine corneas. In vitro, CEC and stromal cell cultures exposed to UV showed generally increased expression of MMP-2, -9, Slug, and Snail; this response was dose and time dependent. Inhibition of the EGFR pathway did not prevent increased expression of MMP-2, -9, Slug or Snail in UV-exposed CEC; however, p38 inhibition did attenuate UV induction.

CONCLUSIONS

We have found increased expression of MMPs in clinical samples of CSK compared to normal corneas. In addition, we have shown that there is a temporal association and dose dependency between UV exposure and production of MMPs, Slug, and Snail. These findings suggest that overexpression of MMPs due to UV-exposure may be linked to changes in the cornea that allow an influx of inflammatory cells and vascularization.

摘要

目的

确定紫外线(UV)辐射是否能调节犬角膜中基质金属蛋白酶(MMP)的表达和调控,并检测犬慢性浅层角膜炎(CSK)中MMPs的表达。

方法

对CSK样本进行MMP-2和MMP-9的免疫组织化学检测。在体外,将犬角膜上皮细胞(CEC)和基质细胞培养物暴露于紫外线照射下。在2、8或24小时后,收集细胞。通过酶谱法检测MMP表达,并使用逆转录聚合酶链反应(RT-PCR)检测Slug和Snail的表达。用表皮生长因子受体(EGFR)抑制剂或p38抑制剂处理的CEC培养物经紫外线照射,24小时后收集,以检测MMPs、Slug和Snail的表达。

结果

与正常犬角膜相比,犬CSK中MMP-2和MMP-9的免疫阳性率增加。在体外,暴露于紫外线的CEC和基质细胞培养物中,MMP-2、-9、Slug和Snail的表达普遍增加;这种反应具有剂量和时间依赖性。抑制EGFR途径并不能阻止紫外线照射的CEC中MMP-2、-9、Slug或Snail表达的增加;然而,抑制p38可减弱紫外线诱导作用。

结论

我们发现与正常角膜相比,CSK临床样本中MMPs的表达增加。此外,我们还表明紫外线暴露与MMPs、Slug和Snail的产生之间存在时间关联和剂量依赖性。这些发现表明,紫外线暴露导致的MMPs过表达可能与角膜变化有关,从而允许炎症细胞流入和血管化。

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