The dynamic microenvironment of pancreatic islet cell transplants precludes the use of common housekeeping genes

G. Shahaf, A. Kassem, J. Levinson, Jared Brazg, E. Lewis
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引用次数: 0

Abstract

Background: Pancreatic islet graft survival is affected by early (<3 days) and late immune responses, displaying local CD3+ T cell predominance and loss of insulin production within a week. However, qRT–PCR gene expression profiles require normalisation to housekeeping genes that might be affected by metabolic, inflammatory, hypoxic, apoptotic, revascularisation–related and immune–cell infiltrate changes. Here, we examined eight housekeeping genes. Methods: Syngeneic and allogeneic mouse islet transplantations were performed; day 1 and 7 grafts were analysed for insulin and CD3 transcript levels, as normalised to each housekeeping gene. Results: Normalised qRT–PCR data was not uniform across transplant combinations and time from transplantation. 18s RNA was the superior housekeeping gene, as confirmed by valid changes in CD3 and insulin expression levels. Conclusions: While β–actin and GAPDH are the least–fitting housekeeping genes for the dynamic microenvironment of islet transplants, 18s RNA maintains authenticity across transplant combinations, time from transplantation and altered immune microenvironment.
胰岛细胞移植的动态微环境排除了普通管家基因的使用
背景:胰岛移植存活受到早期(<3天)和晚期免疫反应的影响,表现为局部CD3+ T细胞优势和一周内胰岛素产生的丧失。然而,qRT-PCR基因表达谱需要对可能受代谢、炎症、缺氧、凋亡、血运重建相关和免疫细胞浸润变化影响的管家基因进行正常化。在这里,我们检查了8个管家基因。方法:采用同基因和异体小鼠胰岛移植;分析第1天和第7天移植物的胰岛素和CD3转录水平,作为每个管家基因的正常化。结果:标准化的qRT-PCR数据在移植组合和移植时间上不一致。正如CD3和胰岛素表达水平的有效变化所证实的那样,18s RNA是优越的管家基因。结论:虽然β -肌动蛋白和GAPDH是胰岛移植动态微环境中最不适合的内源性基因,但18s RNA在移植组合、移植时间和改变的免疫微环境中保持真实性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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