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细胞外基质对猪晶状体上皮细胞增殖和分化的影响。

Effect of extracellular matrix on proliferation and differentiation of porcine lens epithelial cells.

作者信息

de Jong-Hesse Yvonne, Kampmeier Juergen, Lang Gerhard K, Lang Gabriele E

机构信息

Department of Ophthalmology, University of Ulm, Prittwitzstrasse 43, 89075 Ulm, Germany.

出版信息

Graefes Arch Clin Exp Ophthalmol. 2005 Jul;243(7):695-700. doi: 10.1007/s00417-004-1116-3. Epub 2005 Feb 9.

Abstract

BACKGROUND

Proliferation and differentiation of lens epithelial cells (LECs) are important mechanisms of secondary cataract formation. After extracapsular cataract extraction the extracellular matrix (ECM) around the remaining LECs is altered compared with the intact lens. This study investigated the effects of different ECMs on cell proliferation and alpha-smooth muscle actin (alpha-SMA) expression, a marker for myofibroblasts, in cultured porcine LECs.

METHODS

Porcine LECs were cultured for 3 days (cell proliferation assay) or 4 days (alpha-SMA expression) on wells and glass cover slips, respectively, coated with laminin, fibronectin, type I collagen or type IV collagen. LECs cultured on uncoated wells or cover slips served as control. Proliferative response was measured by [(3)H]-thymidine incorporation into DNA. alpha-SMA was detected immunocytochemically with a mouse monoclonal antibody, and the relative numbers of alpha-SMA-positive cells were calculated. Statistical analysis was performed using Student's unpaired t-test.

RESULTS

Cell proliferation was significantly increased by coating with fibronectin (10,320.5+/-6,073 counts per minute; p<0.0001) (mean +/- SD), type I collagen (12,507.3+/-3,914.2 CPM; p<0.0001) and type IV collagen (9,591.4+/-4,088 CPM; p<0.0001) compared with control (1,876.5+/-998 CPM), whereas coating with laminin had no effect (1,760.8+/-812.6 CPM; p=0.7271). The ratio of alpha-SMA-positive LECs cultured on uncoated cover slips for a period of 4 days was 12.2+/-3.51%. This ratio was significantly increased by coating with fibronectin (24.3+/-4.56%; p=0.0001) and type I collagen (21.2+/-8.48%; p=0.0142). Coating with laminin (9.8+/-3.67%; p=0.1682) and type IV collagen (9.0+/-7.09 %; p=0.2491) slightly decreased alpha-SMA expression, but this effect was not statistically significant.

CONCLUSIONS

Fibronectin and type I collagen stimulated both cell proliferation and alpha-SMA expression in cultured porcine LECs. Because fibronectin and type I collagen are not normally present in the adult lens, their possible introduction into the lens capsule after cataract surgery may play a critical role in the development of posterior capsule opacification.

摘要

背景

晶状体上皮细胞(LECs)的增殖和分化是继发性白内障形成的重要机制。囊外白内障摘除术后,与完整晶状体相比,剩余LECs周围的细胞外基质(ECM)发生了改变。本研究调查了不同ECM对培养的猪LECs细胞增殖和α-平滑肌肌动蛋白(α-SMA)表达(成肌纤维细胞的标志物)的影响。

方法

将猪LECs分别在涂有层粘连蛋白、纤连蛋白、I型胶原或IV型胶原的孔板和玻璃盖玻片上培养3天(细胞增殖试验)或4天(α-SMA表达)。在未包被的孔板或盖玻片上培养的LECs作为对照。通过[³H] - 胸腺嘧啶核苷掺入DNA来测量增殖反应。用小鼠单克隆抗体免疫细胞化学检测α-SMA,并计算α-SMA阳性细胞的相对数量。使用学生非配对t检验进行统计分析。

结果

与对照(1,876.5±998计数每分钟;p<0.0001)相比,涂有纤连蛋白(10,320.5±6,073计数每分钟;p<0.0001)、I型胶原(12,507.3±3,914.2 CPM;p<0.0001)和IV型胶原(9,591.4±4,088 CPM;p<0.0001)可显著增加细胞增殖,而涂有层粘连蛋白则无影响(1,760.8±812.6 CPM;p = 0.7271)。在未包被的盖玻片上培养4天的α-SMA阳性LECs的比例为12.2±3.51%。涂有纤连蛋白(24.3±4.56%;p = 0.0001)和I型胶原(21.2±8.48%;p = 0.0142)可显著增加该比例。涂有层粘连蛋白(9.8±3.67%;p = 0.1682)和IV型胶原(9.0±7.09%;p = 0.2491)可使α-SMA表达略有下降,但这种影响无统计学意义。

结论

纤连蛋白和I型胶原可刺激培养的猪LECs的细胞增殖和α-SMA表达。由于纤连蛋白和I型胶原在成年晶状体中通常不存在,白内障手术后它们可能进入晶状体囊膜,这可能在后囊膜混浊的发生中起关键作用。

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