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Release of tissue inhibitor of metalloproteinase-2 from alginate microcapsule encapsulating genetically engineered cells

机译:从藻酸盐微胶囊包封遗传工程细胞的藻酸金属蛋白酶-2组织抑制剂的释放

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Background: In this study, 293T cells were genetically engineered to secrete tissue inhibitor of metalloproteinase-2 (TIMP2) and encapsulated into alginate microcapsules to continuously release TIMP2 protein. Methods: The anti-invasive potential of the microcapsules was studied in vitro using brain tumor cells. The TIMP2 gene was transfected to 293T cells, and genetically engineered 293TIMP2 cells were encapsulated into alginate microcapsules. Release of TIMP2 protein was detected with Western blot analysis and the anti-invasive potential against U87MG cells was tested using gelatin zymography and a Matrigel assay. Results: Cell viability within the alginate microcapsules was maintained at a cell density of 5 × 106. Because polycationic polymers are helpful for maintaining the mechanical strength of microcapsules with good cell viability, the alginate microcapsules were reinforced with chitosan (0.1% w/v). Expression of TIMP2 protein in cell lysates and secretion of TIMP2 into the conditioned medium was confirmed by Western blot analysis. Alginate microcapsules encapsulating 293TIMP2 cells released TIMP2 protein into the medium efficiently, where the TIMP2 protein participated in degradation of the matrix metalloproteinase-2 enzyme and inhibited invasion of U87MG cells. Conclusion: Alginate microcapsules encapsulating 293TIMP2 cells are promising candidates for anti-invasive treatment of glioma.
机译:背景:在本研究中,遗传工程293T细胞以分泌金属蛋白酶-2(TIMP2)的组织抑制剂,并将藻酸盐微胶囊包封成连续释放TIMP2蛋白。方法:使用脑肿瘤细胞在体外研究微胶囊的抗侵入潜力。将TIMP2基因转染至293T细胞,并将遗传工程293timp2细胞包封在藻酸盐微胶囊中。用蛋白质印迹分析检测TIMP2蛋白的释放,并使用明胶酶谱和Matrigel测定来测试针对U87mg细胞的抗侵入潜力。结果:藻酸盐微胶囊内的细胞活力保持在细胞密度为5×1066.因为聚阳离子聚合物有助于保持微胶囊的机械强度具有良好的细胞活力,用壳聚糖加强藻酸盐微胶囊(0.1%w / v) 。通过蛋白质印迹分析证实了Cell裂解物中TIMP2蛋白在细胞裂解物中的表达和TIMP2分泌到条件培养基中。藻酸盐微胶囊封装293点细胞释放TIMP2蛋白,有效地进入培养基中,其中TIMP2蛋白参与了基质金属蛋白酶-2酶的降解并抑制U87mg细胞的侵袭。结论:藻酸盐微胶囊包封293点细胞是胶质瘤的抗侵袭治疗的有希望的候选者。

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