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首页> 外文期刊>Journal of biomedical materials research. Part B, Applied biomaterials. >Time course of transforming growth factor-#beta#_1 (TGF-131) mRNA expression in the host reaction to alginate-poly-L-lysine microcapsules following implantations into rat epididymal fat pads
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Time course of transforming growth factor-#beta#_1 (TGF-131) mRNA expression in the host reaction to alginate-poly-L-lysine microcapsules following implantations into rat epididymal fat pads

机译:植入大鼠附睾脂肪垫后,转化成藻酸盐-聚-L-赖氨酸微胶囊的宿主反应中转化生长因子-#beta#_1(TGF-131)mRNA表达的时间过程

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摘要

Microencapsulation of islets of Langerhans within semipermeable membranes has been proposed to prevent their immune destruction after transplantation. However, the successful application of this method is impaired by a pericapsular reaction, which eventually induces graft failure. Our goal is to study the role of cytokines in the pathogenesis of this reaction, using the model of alginate-poly-L-lysine microcapsule implantation into Wistar rat epididymal fat pads (EFP). The specific objective of this study was to determine the time course of transforming growth factor (TGF)- #beta#_1 mRNA expression by semi-quantitative reverse transcriptase-polymerase chain reaction. Microcapsules induced an increase of TGF-#beta#_1 mRNA expression that reached a maximum 14 days after implantation. Seven, 14, 30, and 60 days after microcapsule implantation, the expression of TGF-#beta#_1 mRNA was significantly higher in pericapsular infiltrate cells than in nonimplanted EFP cells (p < 0.05, p < 0.0001, p < 0.005, and p <0.01, respectively). Injection of physiological saline induced a small and gradual augmentation of TGF-#beta#_1 mRNA expression with a maximum 30 days after injection (p < 0.01 vs. nonimplanted EFP cells). These results demonstrated that microcapsule implantation, in comparison with saline injection, induce an early, extended, and amplified TGF-#beta#_1 mRNA expression. This suggests that TGF-#beta#_1 plays a role in the pathogenesis of the pericapsular host reaction.
机译:已提出将朗格罕氏岛微囊化在半透膜内以防止移植后它们的免疫破坏。但是,这种方法的成功应用会受到包囊周围反应的损害,最终导致移植失败。我们的目标是使用藻酸盐-聚-L-赖氨酸微胶囊植入Wistar大鼠附睾脂肪垫(EFP)的模型研究细胞因子在此反应的发病机理中的作用。这项研究的具体目标是通过半定量逆转录酶-聚合酶链反应确定转化生长因子(TGF)-#beta#_1 mRNA表达的时间过程。微胶囊诱导TGF-#beta#_1 mRNA表达增加,在植入后最多达到14天。微囊植入后第7、14、30和60天,TGF-#beta#_1 mRNA的表达在包膜浸润细胞中明显高于未植入EFP细胞(p <0.05,p <0.0001,p <0.005和p分别<0.01)。注射生理盐水后,在注射后最多30天时会诱导TGF-#beta#_1 mRNA的表达逐渐增加(与未植入的EFP细胞相比,p <0.01)。这些结果表明,与盐水注射相比,微胶囊植入诱导了早期,扩展和扩增的TGF-#beta#_1 mRNA表达。这表明TGF-#beta#_1在包膜周围宿主反应的发病机理中起作用。

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