کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2093721 | 1081974 | 2015 | 11 صفحه PDF | دانلود رایگان |
• Molecular beacon (MB)-based method was developed to purify ventricular CMs from ESCs
• Ventricular CM-specific MBs targeting Irx4 mRNA were successfully generated
• About 98% of the CMs sorted via Irx4-MB displayed ventricular CM-like phenotypes
• Irx4-MB-based purified CMs continuously maintained ventricular CM characteristics
SummaryIsolation of ventricular cardiomyocytes (vCMs) has been challenging due to the lack of specific surface markers. Here we show that vCMs can be purified from differentiating mouse embryonic stem cells (mESCs) using molecular beacons (MBs) targeting specific intracellular mRNAs. We designed MBs (IRX4 MBs) to target mRNA encoding Iroquois homeobox protein 4 (Irx4), a transcription factor specific for vCMs. To purify mESC vCMs, IRX4 MBs were delivered into cardiomyogenically differentiating mESCs, and IRX4 MBs-positive cells were FACS-sorted. We found that, of the cells isolated, ∼98% displayed vCM-like action potentials by electrophysiological analyses. These MB-purified vCMs continuously maintained their CM characteristics as verified by spontaneous beating, Ca2+ transient, and expression of vCM-specific proteins. Our study shows the feasibility of isolating pure vCMs via cell sorting without modifying host genes. The homogeneous and functional ventricular CMs generated via the MB-based method can be useful for disease investigation, drug discovery, and cell-based therapies.
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Journal: - Volume 5, Issue 6, 8 December 2015, Pages 1239–1249