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MCP-1及其受体在wAMD小鼠模型视网膜中的表达及作用机制

周全 肖琳 徐景美 徐冰 Karen Wu 刘晶 卢艳 褚利群

临床与实验病理学杂志2018,Vol.34Issue(1):32-36,5.
临床与实验病理学杂志2018,Vol.34Issue(1):32-36,5.DOI:10.13315/j.cnki.cjcep.2018.01.008

MCP-1及其受体在wAMD小鼠模型视网膜中的表达及作用机制

Expression and function of MCP-1 and its receptor in wAMD model mouse

周全 1肖琳 2徐景美 2徐冰 2Karen Wu 3刘晶 2卢艳 2褚利群2

作者信息

  • 1. 首都医科大学附属北京世纪坛医院 病理科 北京 100038
  • 2. 首都医科大学附属北京世纪坛医院 眼科 北京 100038
  • 3. 美国杜克大学眼科中心,美国北卡罗莱纳州德勒姆市
  • 折叠

摘要

Abstract

Purpose To detect the expression and the function of MCP-1 and its receptor CCR2 in wet agerelated macular degenerative (wAMD) model mouse retina. Methods C57BL/6J mouse were enrolled into the study. Model mouse of wAMD was induced with laser. Frozen sections were prepared for histopathological tests. Immunofluorescence study for MCP-1 and CCR2 was carried out. Co-expression study for CCR2/ CDllb or CCR2/CD68 was carried out. Total protein and total mRNA from the eyes of both wAMD and wild type mouse were extracted. The expression of mRNA and protein of MCP-1 and CCR2 in the eyes were determined by reverse transcription-poly-merase chain reaction (RT-PCR) and Western blots test, respectively. Results In wild type mouse, both MCP-1 and its receptor CCR2 were not detected in the retina. However in wAMD mouse, an obvious up-regulated MCP-1 and CCR2 expression was seen in the retinal pigment epithelium (RPE) cells accompanied with the increased expression of their mRNA and protein. The co-expression study showed that CCR2 co-ex-pressed with CDllb, but not with CD68. Conclusion MCP-1 and its receptor CCR2 may play a role in the wAMD through stimulation of microglia.

关键词

年龄相关性黄斑变性/MCP-1/CCR2/CNV/病理学/临床

Key words

age-related macular degeneration/MCP-1/CCR2/CNV/pathology/clinical

分类

医药卫生

引用本文复制引用

周全,肖琳,徐景美,徐冰,Karen Wu,刘晶,卢艳,褚利群..MCP-1及其受体在wAMD小鼠模型视网膜中的表达及作用机制[J].临床与实验病理学杂志,2018,34(1):32-36,5.

基金项目

北京市卫生系统高层次卫生技术人才(2014-3-049) (2014-3-049)

临床与实验病理学杂志

OA北大核心CSCDCSTPCD

1001-7399

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