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培养的人内皮细胞与涂有热解碳和胶原蛋白的聚对苯二甲酸乙二酯接触后体外细胞因子的表达。

Cytokine expression in vitro by cultured human endothelial cells in contact with polyethylene terephthalate coated with pyrolytic carbon and collagen.

作者信息

Cenni E, Granchi D, Ciapetti G, Savarino L, Corradini A, Di Leo A

机构信息

Istituti Ortopedici Rizzoli, via di Barbiano 1/10, 40136 Bologna, Italy.

出版信息

J Biomed Mater Res. 2000 Jun 15;50(4):483-9. doi: 10.1002/(sici)1097-4636(20000615)50:4<483::aid-jbm3>3.0.co;2-i.

Abstract

In order to evaluate whether or not polyethylene terephthalate coated with pyrolytic carbon and collagen (PET+PC) favors inflammatory or hyperplastic reactions, the expression of mRNAs specific for interleukin-6 (IL-6), platelet-derived growth factor-A (PDGF-A), PDGF-B, transforming growth factor-beta1 (TGF-beta1), and TGF-beta2 were tested in vitro by cultured human umbilical vein endothelial cells (HUVEC). The cultures were put in contact with PET+PC for 1, 24, 48, and 72 h. The same cells cultured on polystyrene without biomaterials were tested as negative controls; cultures incubated with LPS were the positive control. The expression of mRNAs was evaluated by RT-PCR with specific primers. PET+PC did not determine any differences in the expression of IL-6-specific mRNA at any of the incubation times compared to the negative control while LPS (the positive control) induced expression after 24, 48, and 72 h. PET+PC induced a more precocious expression of mRNA specific for PDGF-A than did the negative control; however, the expression no longer was present after 48 h while in the negative control the expression stopped after 72 h. PET+PC induced a less frequent expression of PDGF-B-specific mRNA than did the negative control and LPS, especially after 24 h. PET+PC induced a later expression of TGF-beta2-specific mRNA than did the negative control and a less frequent expression of mRNA specific for TGF-beta1 after 24 and 72 h.

摘要

为了评估涂有热解碳和胶原蛋白的聚对苯二甲酸乙二酯(PET+PC)是否会引发炎症或增生反应,通过培养人脐静脉内皮细胞(HUVEC)在体外检测了白细胞介素-6(IL-6)、血小板衍生生长因子-A(PDGF-A)、PDGF-B、转化生长因子-β1(TGF-β1)和TGF-β2特异性mRNA的表达。将培养物与PET+PC接触1、24、48和72小时。将在没有生物材料的聚苯乙烯上培养的相同细胞作为阴性对照进行检测;用LPS孵育的培养物作为阳性对照。通过使用特异性引物的RT-PCR评估mRNA的表达。与阴性对照相比,PET+PC在任何孵育时间均未导致IL-6特异性mRNA表达的任何差异,而LPS(阳性对照)在24、48和72小时后诱导表达。PET+PC诱导的PDGF-A特异性mRNA表达比阴性对照更早熟;然而,48小时后该表达不再存在,而在阴性对照中,72小时后表达停止。PET+PC诱导的PDGF-B特异性mRNA表达比阴性对照和LPS更少,尤其是在24小时后。PET+PC诱导的TGF-β2特异性mRNA表达比阴性对照更晚,并且在24和72小时后,TGF-β1特异性mRNA的表达频率更低。

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