实验研究
ENGLISH ABSTRACT
白细胞介素-22在大鼠角膜移植术后角膜中的动态表达及其与排斥反应的关系
李萍萍
吴京
马明
于健
王博
作者及单位信息
·
DOI: 10.3760/cma.j.issn.2095-0160.2015.10.004
Dynamic expression of interleukin-22 in grafts after allograft corneal transplantation and its relationship with graft rejection in rats
Li Pingping
Wu Jing
Ma Ming
Yu Jian
Wang Bo
Authors Info & Affiliations
Li Pingping
Department of Ophthalmology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China
Wu Jing
Ma Ming
Yu Jian
Wang Bo
·
DOI: 10.3760/cma.j.issn.2095-0160.2015.10.004
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摘要

背景角膜移植术后的免疫排斥反应仍然是导致角膜移植失败的首要原因,其免疫机制非常复杂。研究证实,辅助性T细胞17(Th17)及其主要效应分子之一白细胞介素-22(IL-22)对心脏、肝脏及骨髓等器官移植方面产生影响,但其在角膜移植排斥反应中的作用尚不确定。

目的探讨IL-22在大鼠角膜移植术后免疫排斥反应中的作用。

方法SPF级雌性SD大鼠24只,SPF级雌性Wistar大鼠76只,体质量180~220 g。按照随机数字表法将受体大鼠随机分为自体角膜移植组、同种异体角膜移植组和同种异体角膜移植抗排斥组,另取4只健康Wistar大鼠作为正常对照组。24只SD大鼠作为供体,48只Wistar大鼠作为受体,行同种异体角膜移植术;24只Wistar大鼠行自体角膜移植术。同种异体角膜移植抗排斥组大鼠术后用妥布霉素地塞米松滴眼液点眼2周。术后每日裂隙灯显微镜下观察大鼠角膜植片情况,参照Larkin等的排斥反应评分标准判断角膜植片的存活情况,采用Kaplan-Meier生存分析法比较各组角膜植片的累积生存率。分别于术后第5天、第14天任意取3只大鼠角膜行组织病理学检查,并于相应时间点任意取各组5只大鼠角膜植片行实时荧光定量PCR检测,计算并比较各组大鼠角膜组织中IL-22 mRNA和配体激活转录因子芳香烃受体(AhR)mRNA的相对表达量。

结果同种异体角膜移植组角膜植片的平均存活时间为10 d,同种异体角膜移植抗排斥组为17 d,差异有统计学意义( χ 2=16.442, P=0.000)。术后不同时间点正常对照组、自体角膜移植组、同种异体角膜移植组和同种异体角膜移植抗排斥组大鼠角膜中IL-22 mRNA的相对表达量总体比较差异均有统计学意义(术后5 d: F=2.44, P=0.00;术后14 d: F=267.92, P=0.00),其中术后5 d和14 d同种异体角膜移植组角膜中IL-22 mRNA的相对表达量均明显高于同种异体角膜移植抗排斥组(术后5 d:9.70±0.35比0.46±0.21;术后14 d:23.12±1.89比3.14±0.94),差异均有统计学意义(均 P<0.05)。术后不同时间点4个组大鼠角膜中AhR mRNA的相对表达量明显不同,总体比较差异均有统计学意义(术后5 d: F=395.73, P=0.00;术后14 d: F=942.37, P=0.00),其中术后5 d和14 d同种异体角膜移植组角膜中AhR mRNA的相对表达量均明显高于同种异体角膜移植抗排斥组(术后5 d:2.52±0.32比1.89±0.10;术后14 d:7.20±0.25比2.60±0.17),差异均有统计学意义(均 P<0.05)。

结论IL-22在发生角膜移植免疫排斥反应的大鼠角膜中呈高表达,妥布霉素地塞米松滴眼液点眼可通过下调IL-22的表达而抑制免疫排斥反应,AhR对IL-22在角膜植片中的表达发挥调控作用。

角膜移植;植片排斥/免疫;辅助T淋巴细胞/免疫;白细胞介素-22;芳香烃受体;妥布霉素地塞米松滴眼液;生物模型;Wistar大鼠
ABSTRACT

BackgroundThe rejection following keratoplasty still is a leading cause of corneal transplantation failure.Studies showed that the interleukin-22 (IL-22), one of the effector molecules of T helper cell 17 (Th17) participated on the rejection after heart, liver and bone marrow transplantation.However, the effect of IL-22 on corneal graft rejection is not well understood.

ObjectiveThis study was to investigate the expression of IL-22 mRNA in the corneal grafts and the role of IL-22 in the immune rejection after corneal transplantation in rats.

MethodsSeventy-two Wistar rats were randomized into autologous keratoplasty group, allograft keratoplasty group and anti-rejection group, and other 4 normal Wistar rats served as normal control group.Autologous keratoplasty was operated on the Wistar rats of the autologous keratoplasty group, and allograft keratoplasty were carried out with the 24 SD rats as donors and 48 Wistar rats as recipients.Tobramycin and dexamethasone eye drops were topically administrated after autologous keratoplasty for 2 weeks in the anti-rejection group.The experimental eyes were examined by slit lamp microscope after surgery and graft survival was evaluated based on the rejection scoring criteria of Larkin.Intergroup accumulated survival rates of grafts were compared using Kaplan-Meier analysis.Histopathological examination of grafts was carried out in 5 and 14 days after operation respectively, and the related expression levels of IL-22 mRNA and aryl hydrocar-bon receptor (AhR) mRNA were carried out by real-time fluorescence quantitative PCR.The feeding and use of the experimental animals followed the Guangdong provincial regulations on the management of experimental animals.The experimental design was approved by the ethics committee of Southern Medical University.

ResultsThe median survival time of grafts in the allograft keratoplasty group was 10 days, and that in the anti-rejection group was 17 days, showing a significant survival extention in the anti-rejection group ( χ 2=16.442, P=0.000). Significant differences were found among the 4 groups in the related expression levels of IL-22 mRNA in both 5 days and 14 days after surgery (postoperative 5 days: F=2.44, P=0.00; postoperative 14 days: F=267.92, P=0.00), and the related expression levels of IL-22 mRNA were remarkably higher in the allograft keratoplasty group than those in the anti-rejection group at different time points (postoperative 5 days: 9.70±0.35 vs.0.46±0.21; postoperative 14 days: 23.12±1.89 vs.3.14±0.94 ) (both at P<0.05). The related expression levels of AhR mRNA in the grafts were considerably different among the 4 groups (postoperative 5 days: F=395.73, P=0.00; postoperative 14 days: F=942.37, P=0.00), and the expression levels were significantly elevated in the allograft keratoplasty group compared with the anti-rejection group at various time points (postoperative 5 days: 2.52±0.32 vs. 1.89±0.10; postoperative 14 days: 7.20±0.25 vs.2.60±0.17) (both at P<0.05).

ConclusionsThe expression level of IL-22 RNA up-regulates in the grafts with immuno-rejection.Topical administration of tobramycin and dexamethasone eye drops inhibits the rejection after keratoplasty.AhR plays a regulative role to the expression of IL-22 in rats after keratoplasty.

Corneal transplantation;Graft rejection/immunology;T-lymphocytes, helper-inducer/immunology;Interleukin-22;Receptors, aryl hydrocarbon;Eye drops, tobramycin and dexamethasone;Models, biological;Rats, Wistar
Wu Jing, Email: mocdef.uabmmifgnijuw
引用本文

李萍萍,吴京,马明,等. 白细胞介素-22在大鼠角膜移植术后角膜中的动态表达及其与排斥反应的关系[J]. 中华实验眼科杂志,2015,33(10):881-886.

DOI:10.3760/cma.j.issn.2095-0160.2015.10.004

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角膜病是中国主要的致盲眼病之一,目前角膜移植术是治疗角膜盲可靠、有效的复明手段。角膜属于免疫赦免器官,因此角膜移植术植片成活率较高,但是角膜移植术后的免疫排斥反应仍然是导致手术失败的首要原因。器官移植术后的免疫排斥反应是一个由多种细胞及活化因子共同参与的、复杂的免疫应答过程。近年来的研究证实,辅助性T细胞17(T helper cell 17,Th17)及其主要效应分子白细胞介素-17(interleukin-17,IL-17)在器官移植免疫排斥反应中发挥重要作用 [ 1 ],此外IL-22也是Th17细胞重要的效应分子 [ 2 , 3 ]。IL-22的表达依赖于Notch-配体依赖型芳香烃受体(aryl hydrocarbon receptor,AhR)信号通路的调控,其中Notch信号主要通过刺激配体依赖性转录因子AhR来上调IL-22的表达 [ 4 ]。目前已开展了IL-22对心脏、肝脏及骨髓等器官移植方面影响的研究 [ 5 , 6 , 7 ],但其在大鼠角膜移植排斥反应中的作用尚不确定。本研究中建立同种大鼠角膜移植模型,采用荧光定量PCR技术检测大鼠角膜组织中IL-22 mRNA的表达变化,探讨IL-22在角膜移植排斥反应中的作用。
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备注信息
A
吴京,Email: mocdef.uabmmifgnijuw
B
国家自然科学基金项目 (81170887)
广东省自然科学基金项目 (S2013010016640、S2012010008946、9151051501000047)
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