Han Yan-ping, Zhao Lu-hang, Wu Hai-ming
Department of Biochemistry and Molecular Biology, College of Medicine, Zhejiang University, Hangzhou 310006, China.
Zhejiang Da Xue Xue Bao Yi Xue Ban. 2006 May;35(3):265-72. doi: 10.3785/j.issn.1008-9292.2006.03.007.
To study the mechanism of oligochitosan-induced macrophage activation.
Oligochitosan was chemically modified with fluorophore 2-aminoacridone (2-AMAC). The cellular events of 2-AMAC-oligochitosan-macrophage interaction were analyzed with confocal laser microscopy and the fluorescence intensity of cells was analyzed by BD LSR flow cytometer. The mechanism of oligochitosan uptake by macrophages was studied by competitive inhibition test and the effect of calcium, trypsin and colchicine on oligochitosan recognition and internalization were also determined. RT-PCR was performed to investigate the level of TNF-alpha secretion.
Macrophage could bind and uptake oligochitosan, which was dependent on the temperature: the uptake proceeded rapidly at 37 degrees C and at 4 degrees C macrophage could only bind oligochitosan. EDTA decreased oligochitosan uptake. Trypsin treatment significantly reduced the internalization, and uptake was recovered by trypsin termination. Colchicine significantly inhibited the internalization process and was dose dependent. 0.1 mol/L mannose inhibited TNF-alpha expression induced by oligochitosan.
Macrophage could uptake oligochitosan via mannose receptor mediated pinocytosis. Mannose receptor is crucial for the oligochitosan-induced macrophages activation.
研究低聚壳聚糖诱导巨噬细胞活化的机制。
用荧光团2-氨基吖啶酮(2-AMAC)对低聚壳聚糖进行化学修饰。采用共聚焦激光显微镜分析2-AMAC-低聚壳聚糖-巨噬细胞相互作用的细胞事件,并用BD LSR流式细胞仪分析细胞的荧光强度。通过竞争性抑制试验研究巨噬细胞摄取低聚壳聚糖的机制,同时测定钙、胰蛋白酶和秋水仙碱对低聚壳聚糖识别和内化的影响。采用RT-PCR检测肿瘤坏死因子-α(TNF-α)的分泌水平。
巨噬细胞能够结合并摄取低聚壳聚糖,这一过程依赖于温度:在37℃时摄取迅速,而在4℃时巨噬细胞只能结合低聚壳聚糖。乙二胺四乙酸(EDTA)降低了低聚壳聚糖的摄取。胰蛋白酶处理显著降低了内化作用,而终止胰蛋白酶处理后摄取得以恢复。秋水仙碱显著抑制内化过程,且呈剂量依赖性。0.1 mol/L甘露糖抑制低聚壳聚糖诱导的TNF-α表达。
巨噬细胞可通过甘露糖受体介导的胞吞作用摄取低聚壳聚糖。甘露糖受体对低聚壳聚糖诱导的巨噬细胞活化至关重要。