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首页> 外文期刊>Diabetes >Transfection of Human Pancreatic Islets With an Anti-Apoptotic Gene (bcl-2) Protects β-Cells From Cytokine-Induced Destruction
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Transfection of Human Pancreatic Islets With an Anti-Apoptotic Gene (bcl-2) Protects β-Cells From Cytokine-Induced Destruction

机译:用抗凋亡基因(bcl-2)转染人胰岛可保护β细胞免受细胞因子诱导的破坏

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摘要

Apoptosis has been identified as a mechanism of pan- creatic islet β-cell death in autoimmune diabetes. Proinflammatory cytokines are candidate mediators of β-cell death in autoimmune diabetes, and these cytokines can induce β-cells death by apoptosis. In the present study, we examined whether transfection of human islet β-cells with an anti-apoptotic gene, bcl-2, can prevent cytokine-induced β-cell destruction. Human islet β-cells were transfected by a replication- Defective herpes simplex virus (HSV) amplicon vector That expressed the bcl-2 gene (HSVbcl-2) and, as a con- Trol, the same HSV vector that expressed a β-galac- Tosidase reporter gene (HSVlac).
机译:细胞凋亡已被确定为自身免疫性糖尿病中胰岛β细胞死亡的机制。促炎细胞因子是自身免疫性糖尿病中β细胞死亡的候选介质,这些细胞因子可通过凋亡诱导β细胞死亡。在本研究中,我们检查了用抗凋亡基因bcl-2转染人胰岛β细胞是否可以预防细胞因子诱导的β细胞破坏。用表达bcl-2基因的复制缺陷型单纯疱疹病毒(HSV)扩增子载体(HSVbcl-2)转染人胰岛β细胞,并使用表达β-半乳清蛋白的相同HSV载体转染人类胰岛β细胞。 -糖苷酶报道基因(HSVlac)。

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