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姜黄素对角膜基质细胞纤维化的抑制作用
引用本文:李小磊,宋秀君,卢建民,王会芳,张晓融. 姜黄素对角膜基质细胞纤维化的抑制作用[J]. 眼科研究, 2011, 29(5): 402-406. DOI: 10.3760/cma.j.issn.2095-0160.2011.05.005
作者姓名:李小磊  宋秀君  卢建民  王会芳  张晓融
作者单位:河北医科大学第三医院眼科,石家庄,050000
摘    要:背景角膜的创伤或手术可导致角膜基质细胞纤维化,进而形成瘢痕。研究表明姜黄素可明显减轻组织的纤维化程度,但姜黄素是否会影响角膜基质细胞纤维化的研究尚少。目的观察不同质量浓度的姜黄素对小鼠角膜基质细胞向成纤维细胞转化过程的影响,探讨姜黄素抗角膜基质纤维化的作用。方法150只6~8周龄BALB/c小鼠,分离角膜基质细胞并在含质量分数10%胎牛血清(FBS)的DMEM中进行培养,以原代角膜基质细胞重悬于DMEM中并分为5组:(1)空白对照组(DMEM+10%FBS,含质量分数1%。DMSO,CG组)。(2)低剂量组(CG+7.5mg/L姜黄素组)。(3)中剂量组(CG+10mg/L姜黄素组)。(4)高剂量组(CG+12.5mg/L姜黄素组)。(5)无诱导剂组(DMEM,含1%oDMSO)。上述因素干预7d后,用逆转录聚合酶链反应(RT—PCR)法检测各组中细胞表型keratocan、醛脱氢酶(ALDH)、CD90、decorin、fibronectin一1的表达。用MTS法检测姜黄素对角膜基质细胞增生的影响。制备小鼠角膜冰冻切片,采用免疫荧光技术检测角膜基质细胞内fibronectin-1的表达。结果原代培养的角膜基质细胞呈梭形,为细胞质丰富且核大的角膜基质成纤维细胞。随着姜黄素质量浓度的增加,角膜基质细胞中keratocanmRNA、ALDHmRNA的表达量增加,CD90mRNA和decorinmRNA的表达量减少,差异均有统计学意义(P〈O.05),fibronectin-1mRNA的表达变化差异无统计学意义(P〉0.05)。MTS法检测发现,随着姜黄素质量浓度的增加,对角膜基质细胞增生的抑制率逐渐增加(F=956.00,P〈0.05)。免疫荧光技术检测发现角膜基质细胞中fibronectin-1的表达呈红色荧光。结论姜黄素对离体小鼠角膜基质细胞纤维化有明显的抑制作用,可减轻角膜基质创伤修复过程中的过度纤维化。

关 键 词:姜黄素  角膜基质细胞  成纤维细胞  纤维化

Inhibitory effect of curcumin on corneal keratocytes fibrosis
LI Xiao-lei,SONG Xiu-jun,LU Jian-min,WANG Hui-fang,ZHANG Xiao-rong. Inhibitory effect of curcumin on corneal keratocytes fibrosis[J]. Chinese Ophthalmic Research, 2011, 29(5): 402-406. DOI: 10.3760/cma.j.issn.2095-0160.2011.05.005
Authors:LI Xiao-lei  SONG Xiu-jun  LU Jian-min  WANG Hui-fang  ZHANG Xiao-rong
Affiliation:. (Department of Ophthalmology, Third Hospital of Hebei Medical University, Shijiazhuang 050000, China)
Abstract:Background The injury or surgery of cornea cause the proliferation of corneal stromal cells and scar formation.Recent research showed that cureumin can obviously reduce the degree of fibrosis of tissue.But if curcumm play inhibitory effect on corneal keratocytes fibrosis is rarely reported.Objecttve This studv was to investigate the effect of curcumin on the transformation of corneal keratocytes into fibroblasts in vitro and further explore the antifibrotic effect of curcumin on corneal keratocytes.Methods The murine corneal keratocytes from 150 BALB/c mice were isolated and primary culture in DMEM culture medium containing 10% fetal bovine serum and then divided into blank control group(inducer group,CG),low-dose group(CG+7.5 mg/L curcumin),mediumdose group(CG+10.0 mg/L curcumin),high-dose group(CG+12.5 mg/L curcumin),non-inducer group.Seven days following intervention,the expression of cell markers such as keratocan,aldehyde dehydrogenase(ALDH),decorin and fibronectin-1 in keratocytes were analyzed by RT-PCR.The effect of curcumin on cultured murine corneal keratocytes proliferation was evaluated by MTS technique.The expression of fibronectin-1 in murine cornea was investigated by immunofluorescence assay.Results The primarily cultured keratocytes showed tlIe fusiform-like shape with the abundant cytoplasm and big nuclei.In the presence of curcumin,the mRNA levels of keratocan and ALDH were down-regulated and those of CD90 and decorin were up-regulated,showing the significantly differences with the increase of dose(P<0.05),but the expression pf fibronectin-i was not obviously changed with the alteration of dose of curcumin. MTS showed that the inhibitory rates of curcumin on keratocytes in 10.0 mg/L and 2. 5 mg/L groups were enhanced in comparison with 7.5 mg/L group, showing statistically significant difference among three groups( F = 956.00, P<0.05). The expression of fibronectin-1 was found in the corneal keratocytes with the red fluorescence in stroma. Conclusion Curcumin can inhibit the fibrosis of corneal keratoeytes in a dose-dependent manner. These results offer a preliminary theoretical basis for the application of curcumin in controlling corneal scar formation during wound healing.
Keywords:Curcumin  Keratocyte  Fibroblast  Fibrosis
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