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基质金属蛋白酶-8对干眼症条件下碱烧伤角膜的地塞米松治疗至关重要。

MMP-8 Is Critical for Dexamethasone Therapy in Alkali-Burned Corneas Under Dry Eye Conditions.

作者信息

Bian Fang, Wang Changjun, Tukler-Henriksson Johanna, Pflugfelder Stephen C, Camodeca Caterina, Nuti Elisa, Rossello Armando, Li De-Quan, de Paiva Cintia S

机构信息

Department of Ophthalmology, Baylor College of Medicine, Houston, Texas.

Division of Immunology, Transplants and Infectious Diseases, San Raffaele Scientific Institute, Milan, Italy.

出版信息

J Cell Physiol. 2016 Nov;231(11):2506-16. doi: 10.1002/jcp.25364. Epub 2016 Mar 28.

DOI:10.1002/jcp.25364
PMID:26923552
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4946998/
Abstract

Our previous studies have shown that Dexamethasone (Dex) reduced the expression of matrix-metalloproteinases (MMPs -1,-3,-9,-13), IL-1β and IL-6, while it significantly increased MMP-8 mRNA transcripts in a concomitant dry eye and corneal alkali burn murine model (CM). To investigate if MMP-8 induction is responsible for some of the protective effects of Dex in CM, MMP-8 knock out mice (MMP-8KO) were subjected to the CM for 2 or 5 days and topically treated either with 2 μl of 0.1% Dexamethasone (Dex), or saline QID. A separate group of C57BL/6 mice were topically treated with Dex or BSS and received either 100 nM CAM12 (MMP-8 inhibitor) or vehicle IP, QD. Here we demonstrate that topical Dex treated MMP-8KO mice subjected to CM showed reduced corneal clarity, increased expression of inflammatory mediators (IL-6, CXCL1, and MMP-1 mRNA) and increased neutrophil infiltration at 2D and 5D compared to Dex treated WT mice. C57BL/6 mice topically treated with Dex and CAM12 IP recapitulated findings seen with MMP-8KO mice. These results suggest that some of the anti-inflammatory effects of Dex are mediated through increased MMP-8 expression. J. Cell. Physiol. 231: 2506-2516, 2016. © 2016 Wiley Periodicals, Inc.

摘要

我们之前的研究表明,在干眼和角膜碱烧伤小鼠模型(CM)中,地塞米松(Dex)可降低基质金属蛋白酶(MMP-1、-3、-9、-13)、白细胞介素-1β(IL-1β)和白细胞介素-6(IL-6)的表达,同时显著增加MMP-8的mRNA转录物。为了研究MMP-8的诱导是否对地塞米松在CM中的一些保护作用负责,将MMP-8基因敲除小鼠(MMP-8KO)进行CM处理2天或5天,并分别用2μl的0.1%地塞米松(Dex)或生理盐水进行每日4次的局部治疗。另一组C57BL/6小鼠局部用Dex或平衡盐溶液(BSS)处理,并腹腔注射100 nM的CAM12(MMP-8抑制剂)或溶剂,每日1次。在此我们证明,与Dex处理的野生型小鼠相比,接受CM处理的局部用Dex治疗的MMP-8KO小鼠在第2天和第5天时角膜透明度降低,炎症介质(IL-6、CXCL1和MMP-1 mRNA)表达增加,中性粒细胞浸润增加。局部用Dex和腹腔注射CAM12的C57BL/6小鼠重现了MMP-8KO小鼠的研究结果。这些结果表明,地塞米松的一些抗炎作用是通过增加MMP-8的表达介导的。《细胞生理学杂志》2016年第231卷:2506 - 2516页。© 2016威利期刊公司

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f12/4946998/0c4036e25a24/nihms-777213-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f12/4946998/6d10b999d928/nihms-777213-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f12/4946998/f3a4a7d72269/nihms-777213-f0002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f12/4946998/0c4036e25a24/nihms-777213-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f12/4946998/6d10b999d928/nihms-777213-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f12/4946998/f3a4a7d72269/nihms-777213-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f12/4946998/0002206f9f4a/nihms-777213-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f12/4946998/8aa9e5d4a4ad/nihms-777213-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f12/4946998/0c4036e25a24/nihms-777213-f0005.jpg

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