期刊文献+

小鼠视网膜激光损伤早期组织功能学变化与单核细胞趋化蛋白动态表达关系的研究 被引量:3

Correlation between pathological and functional changes of the retina and the expression of monocyte chemoattractant protein after retinal laser injury in mice
原文传递
导出
摘要 目的 观察小鼠视网膜激光损伤后早期组织功能变化及单核细胞趋化蛋白(MCP-1)表达水平,初步探讨两者之间的关系.方法 116只C57BL/6小鼠随机分为正常组、激光损伤组,均为58只.采用激光光凝方式建立视网膜激光损伤模型.分别于激光光凝后1、3、7d行视网膜电图(ERG)检查.激光光凝后1、3、7d分别处死正常组、激光损伤组小鼠并摘除眼球.行苏木精-伊红染色观察视网膜组织形态变化,实时定量聚合酶链反应(PCR)检测各组小鼠视网膜中MCP-1的基因相对表达情况,蛋白质免疫印迹法(Western blot)检测视网膜中MCP-1的蛋白表达情况.结果 光学显微镜观察结果显示,随激光损伤时间延长,视网膜组织结构损伤进行性加重.ERG检测结果显示,激光损伤后1、3、7d,正常组、激光损伤组小鼠暗适应a(t=6.998、9.594、13.778)、b波(t=12.089、13.310、21.989)振幅比较,差异有统计学意义(P=0.000).激光损伤后1d,正常组、激光损伤组明适应a波振幅比较,差异无统计学意义(t=2.659,P=0.200),b波振幅比较,差异有统计学意义(t=8.844,P=0.000);3、7d,明适应a(t=3.076、7.544)、b波(t=10.418、8.485)振幅比较,差异均有统计学意义(P=0.000).激光损伤后1、3 d(t=3.773)及1、7d(t=5.070)暗适应a波振幅比较,差异有统计学意义(P<0.01),3、7d比较,差异无统计学意义(t=1.297,P=0.660);b波振幅,1、7d比较,差异有统计学意义(t=4.762,P=0.000);1、3 d(t=2.236)及3、7 d(t=2.526)比较,差异无统计学意义(P=0.120、0.060).明适应a波振幅,1、7d比较,差异有统计学意义(t=2.991,P=0.020);1、3 d(t=0.516)及3、7 d(t=2.475)比较,差异均无统计学意义(P=1.000、0.710);b波振幅,1、3 d(t=3.570)及1、7 d(t=4.989)比较,差异均有统计学意义(P<0.01),3、7d比较,差异无统计学意义(t=1.419,P=0.070).实时定量PCR检测结果显示,激光损伤后1、3、7d,激光损伤组MCP-1基因相对表达量与正常组比较,差异均有统计学意义(t=14.329、16.861、5.743,P<0.05).Western blot检测结果显示,激光损伤后1、3、7d,激光损伤组MCP-1蛋白相对表达量与正常组比较,差异均有统计学意义(t=75.068、54.145、14.653,P<0.05).结论 小鼠视网膜激光损伤后7d内,视网膜组织结构和功能损害进行性加重,且程度与MCP-1表达相关. Objective To investigate the relationship between the pathological and functional changes of the retina and the expression of monocyte chemoattractant protein (MCP)-1 after retinal laser injury in mice.Methods A total of 116 C57BL/6 mice were randomly divided into the normal group (58 mice) and the injured group (58 mice).Retinal laser injuries were induced by Argon ion laser.At 1,3,7 days after laser injury,electroretinogram (ERG) responses were recorded to detect the function of the retina.Hematoxylin and eosin (HE) staining was performed to observe pathological changes.Quantitative real-time polymerase chain reaction (PCR) was performed to detect gene expression of MCP-1.Western blot was used to measure the protein expression of MCP-1.Results HE staining showed a progressive damage of the retinal structure.The results of ERG showed that the differences of dark-adaptive a wave (t =6.998,9.594,13.778) and b wave (t=12.089,13.310,21.989) amplitudes of 1,3 and 7 day post-injury between normal group and injured group were statistically significant (P =0.000).At 1 day post-injury,the differences of light adaptive b wave amplitudes between the two groups were statistically significant (t =8.844,P=0.000).While the differences of light-adaptive a wave amplitudes were not (t=2.659,P=0.200).At 3,7 days post-injury,the differences of a (t=3.076,7.544) and b wave amplitudes (t=10.418,8.485) between the two groups were statistically significant (P=0.000).In dark-adaptive ERG,the differences of a wave amplitudes between 1 day and 3 days (t=3.773),1 day and 7 days (t=5.070) and b wave amplitudes between 1 day and 7 days (t=4.762) were statistically significant (P〈0.01),while the differences of a wave amplitudes between the 3 days and 7 days (t=1.297) and b wave amplitudes between 1dayand 3 days (t=2.236),3 day and 7 days (t=2.526) were not significant (P=0.660,0.120,0.060).In light-adaptive ERG,the differences of a wave amplitudes between 1 day and 7 days (t=2.992)and b wave amplitudes between 1 day and 3 days (t=3.570),1day and 7 days (t=4.989) were statistically significant (P〈0.05),while the differences of a wave amplitudes between 1 day and 3 days (t=0.516),the 3 days and 7 days (t=2.475) and b wave amplitudes between 3 days and 7 days (t=1.419) were not significant (P=1.000,0.710,0.070).Quantitative real-time PCR showed that the differences of MCP-1 gene expression at 1,3 and 7 day post-injury between normal group and injured group were statistically significant (t=14.329,16.861,5.743; P〈0.05).Western blot showed that the differences of MCP-1 protein expression at 1,3 and 7 day post-injury between normal group and injured group were statistically significant (t=75.068,54.145,14.653; P〈0.05).Conclusion In the first 7 days after mice retinal laser injury,there are progressive pathological and functional damage of the retina,which might be correlated with MCP-1 expression.
出处 《中华眼底病杂志》 CAS CSCD 北大核心 2014年第5期495-499,共5页 Chinese Journal of Ocular Fundus Diseases
基金 国家自然科学基金
关键词 视网膜疾病/病因学 视网膜电描记术 趋化因子CCL2 动物实验 CHEMOKINE CCL2 Retina diseases/etiology Electroretinography Animal experimentation
作者简介 通信作者:李筱荣,Email:xiaorli@163.com
  • 相关文献

参考文献17

  • 1Deshmane SL,Kremlev S,Amini S,et al.Monocyte chemoattractant protein-1 (MCP-1).:an overview[J].J Interferon Cytokine Res,2009,29:313-326.
  • 2Marshall J,Bird AC.A comparative histopathological study of argon and krypton laser irradiations of the human retina[J].Br J Ophthalmol,1979,63:657-668.
  • 3Lambert V,Lecomte J,Hansen S,et al.Laser-induced choroidal neovascularization model to study age-related macular degeneration in mice[J].Nat Protoc,2013,8:2197-2211.
  • 4Ng TF,Turpie B,Masli S.Thrombospondin-1-mediated regulation of microglia activation after retinal injury[J].Invest Ophthalmol Vis Sci,2009,50.:5472-5478.
  • 5蒋元丰,张晓敏,张琰,张丽娟,张灵君,刘勋,李筱荣.尾静脉注射骨髓间充质干细胞对小鼠视网膜激光损伤后细胞凋亡的影响[J].中华眼底病杂志,2013,29(1):67-71. 被引量:4
  • 6Belokopytov M,Shulman S,Dubinsky G,et al.Intravitreal saline injection ameliorates laser-induced retinal damage in rats[J].Retina,2012,32:1165-1170.
  • 7Ben-Shlomo G,Belokopytov M,Rosner M,et al.Functional deficits resulting from laser-induced damage in the rat retina[J].Lasers Surg Med,2006,38:689-694.
  • 8Suzuki M,Ozawa Y,Kubota S,et al.Neuroprotective response after photodynamic therapy:role of vascular endothelial growth factor[J].J Neuroinflammation,2011,8:176.
  • 9Kasaoka M,Ma J,Lashkari K.c-Met modulates RPE migratory response to laser-induced retinal injury[J/OL].PLoS One,2012,7.:40771[2012-07-13].http://www.plosone.org/article/info:doi/10.1371/journal.pone.0040771? imageURI =info:doi/10.1371/journal.pone.0040771.g002.
  • 10Liang KJ,Lee JE,Wang YD,et al.Regulation of dynamic behavior of retinal microglia by CX3CR1 signaling[J].Invest Ophthalmol Vis Sci,2009,50:4444-4451.

二级参考文献22

  • 1Bull ND,Martin KR. Concise review:toward stem cell-based therapies for retinal neurodegenerative diseases[J].Stem Cells,2011.1170-1175.
  • 2Wong IY,Poon MW,Pang RT. Promises of stem cell therapy for retinal degenerative diseases[J].Greefe's Archive for Clinical and Experimental Ophthalmology,2011.1439-1448.
  • 3Huang Y,Enzmann V,Ildstad ST. Stem cell-based therapeutic applications in retinal degenerative diseases[J].Stem Cell Rev,2011.434-445.
  • 4Tibbetts MD,Samuel MA,Chang TS. Stem cell therapy for retinal disease[J].Current Opinion in Ophthalmology,2012.226-234.
  • 5Ying HS,Symons RC,Lin KL. Accidental Nd:YAG laser-induced choroidal neovascularization[J].Lasers in Surgery and Medicine,2008.240-242.
  • 6Zobor D,Zrenner E. Retinitis pigmentosa-a review[A].Ophthalmologe,2012.501-515.
  • 7Bouhenni RA,Dunmire J,Sewell A. Animal models of glaucoma[OL].Journal of Biomedicine and Biotechnology,2012.692609.
  • 8Ambati J,Fowler BJ. Mechanisms of age-related macular degeneration[J].Neuron,2012.26-39.
  • 9Barkana Y,Belkin M. Laser eye injuries[J].Survey of Ophthalmology,2000.459-478.
  • 10Ben-Shlomo G,Belokopytov M,Rosner M. Functional deficits resulting from laser-induced damage in the rat retina[J].Lasers in Surgery and Medicine,2006.689-694.

共引文献3

同被引文献29

  • 1郭锐,朱长乐,王育良.太子参皂苷提取物对视网膜激光损伤的保护作用[J].眼科新进展,2013,33(12):1120-1123. 被引量:6
  • 2LEE CJ, SMITH JH, KANG-Mieler J J, BUDZYNSKI E, LINSEN- MEIER RA. Decreased circulation in the feline choriocapil- larks underlying retinal photocoagulation lesions [ J ]. Invest Ophthalmol Vis Sci, 2011,52 ( 6 ) : 3398 -3403.
  • 3MUQIT MM,GRAY JC,MARCEI,IJNO GR,HENSON DB,YOUNG LB, PATTON N, et al. In vivo laser-tissue interactions and healing responses from 20-VS 100-millisecond pulse Pastal photocoagulation burns[ J ]. Arch Ophthalmol,2010,128 (4) : 448-455.
  • 4SCANLON PH,STRATrON IM,HISTED M, CHAVE SJ,ALD- INGTON SJ. The influence of background diabetic retinopa- thy in the second eye on rotes of progression of diabetic reti- nopathy between 2005 and 2010[ J ]. Acta Ophtha/mo/,2013, 91 (5) : e335-339.
  • 5CHAPPELOW AV, TAN K, WAHEED NK, KAISER PK. Panret- inal photocoagulation for proliferative diabetic retinopathy: pattern scan laser versus argon laser[ J]. Am J Ophthalmol, 2012,153 ( 1 ) : 137-142.
  • 6CHOU JC,ROLLINS SD,YE M,BATLLE D ,FAWZI AA. Endo- thelin receptor-A antagonist attenuates retinal vascular and neuroreIXnal pathology in diabetic mice [ J ]. Invest Ophthal- tool V/s Sc/,2014,55(4) :2516-2525.
  • 7LUTFRULL JK, SRAMEK C, PALANKER D, SPINK CJ, MUSCH DC. Long-term safety, high-resolution imaging, and tissue tem- perature modeling of subvisible diode micropulse photocoag- ulation for retinovascular macular edema [ J ]. Retina, 2012, 32(2) :375-385.
  • 8DEMIR M, OBA E, GUVEN D, ACAR Z, CINAR S. Results of intravitreal triameinolone aeetonide in patients with maeular edema secondary to branch retinal vein occlusion [ J ]. Int J Clin Pharm,2014,36(2) :438-442.
  • 9MUQIT MM, DENNISS J, NOURRIT V, MARCELLINO GR, HENSON DB, SCHIESSL I, et al. Spatial and spectral ima- ging of retinal laser photocoagulation burns[ J]. Invest Oph- thalmol Vis Sci,2011,52( 2 ) :994-1002.
  • 10MEHLSEN J, ERLANDSEN M, POULSEN PL, BEK T. Identi- fication of independent risk factors for the development of diabetic retinopathy requiring treatment [ J ]. Acta Ophthal- mol,2011,89(6) :515-521.

引证文献3

二级引证文献14

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部