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光遗传学报告基因作为 mRNA 递送至人心肌细胞诱导物中可重复评估动作电位和钙处理。

Optogenetic Reporters Delivered as mRNA Facilitate Repeatable Action Potential and Calcium Handling Assessment in Human iPSC-Derived Cardiomyocytes.

机构信息

Department of Anatomy and Embryology, Leiden University Medical Center, Leiden, The Netherlands.

Department of Applied Stem Cell Technologies, University of Twente, Enschede, The Netherlands.

出版信息

Stem Cells. 2022 Jul 27;40(7):655-668. doi: 10.1093/stmcls/sxac029.

Abstract

Electrical activity and intracellular Ca2+ transients are key features of cardiomyocytes. They can be measured using organic voltage- and Ca2+-sensitive dyes but their photostability and phototoxicity mean they are unsuitable for long-term measurements. Here, we investigated whether genetically encoded voltage and Ca2+ indicators (GEVIs and GECIs) delivered as modified mRNA (modRNA) into human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) would be accurate alternatives allowing measurements over long periods. These indicators were detected in hiPSC-CMs for up to 7 days after transfection and did not affect responses to proarrhythmic compounds. Furthermore, using the GEVI ASAP2f we observed action potential prolongation in long QT syndrome models, while the GECI jRCaMP1b facilitated the repeated evaluation of Ca2+ handling responses for various tyrosine kinase inhibitors. This study demonstrated that modRNAs encoding optogenetic constructs report cardiac physiology in hiPSC-CMs without toxicity or the need for stable integration, illustrating their value as alternatives to organic dyes or other gene delivery methods for expressing transgenes.

摘要

电活动和细胞内 Ca2+ 瞬变是心肌细胞的关键特征。可以使用有机电压和 Ca2+ 敏感染料进行测量,但它们的光稳定性和光毒性意味着它们不适合长期测量。在这里,我们研究了作为修饰后的 mRNA(modRNA)递送到人诱导多能干细胞衍生的心肌细胞(hiPSC-CMs)中的遗传编码电压和 Ca2+ 指示剂(GEVIs 和 GECIs)是否会成为允许长时间测量的准确替代品。在转染后长达 7 天的时间里,这些指示剂在 hiPSC-CMs 中被检测到,并且不会影响对致心律失常化合物的反应。此外,使用 GEVI ASAP2f,我们观察到长 QT 综合征模型中的动作电位延长,而 GECI jRCaMP1b 则便于重复评估各种酪氨酸激酶抑制剂的 Ca2+ 处理反应。这项研究表明,编码光遗传学构建体的 modRNA 在 hiPSC-CMs 中报告心脏生理学而没有毒性或需要稳定整合,说明了它们作为有机染料或其他基因传递方法的替代品表达转基因的价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10a6/9332902/ff44c1286fc2/sxac029f0007.jpg

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