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Lentiviral Mediated Delivery of shRNAs to hESCs and NPCs Using Low-cost Cationic Polymer Polyethylenimine (PEI). | LitMetric

Lentiviral Mediated Delivery of shRNAs to hESCs and NPCs Using Low-cost Cationic Polymer Polyethylenimine (PEI).

J Vis Exp

Department of Biochemistry and Molecular Biology, College of Medicine and Health Sciences, United Arab Emirates University; Zayed Center for Health Sciences, United Arab Emirates University;

Published: May 2022

AI Article Synopsis

  • The protocol details the use of lentiviral particles to efficiently deliver short hairpin RNAs (shRNAs) to human embryonic stem cells (hESCs) and neural progenitor cells (NPCs) derived from hESCs.
  • Lentiviral particles are created by co-transfecting HEK293T cells with plasmids carrying shRNAs and packaging plasmids, and are concentrated using ultracentrifugation, achieving high viral titers.
  • The method successfully shows stable expression of shRNAs in hESCs and transient expression in NPCs, while maintaining the cells' ability to differentiate into various central nervous system lineages.

Article Abstract

The current protocol describes the use of lentiviral particles for the delivery of short hairpin RNAs (shRNAs) to both human embryonic stem cells (hESCs) as well as neural progenitor cells (NPCs) derived from hESCs at high efficiency. Lentiviral particles were generated by co-transfecting HEK293T cells using entry vectors (carrying shRNAs) along with packaging plasmids (pAX and pMD2.G) using the low-cost cationic polymer polyethylenimine (PEI). Viral particles were concentrated using ultracentrifugation, which resulted in average titers above 5 x 10. Both hESCs and NPCs could be infected at high efficiencies using these lentiviral particles, as shown by puromycin selection and stable expression in hESCs, as well as transient GFP expression in NPCs. Furthermore, western blot analysis showed a significant reduction in the expression of genes targeted by shRNAs. In addition, the cells retained their pluripotency as well as differentiation potential, as evidenced by their subsequent differentiation into different lineages of CNS. The current protocol deals with the delivery of shRNAs; however, the same approach could be used for the ectopic expression of cDNAs for overexpression studies.

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Source
http://dx.doi.org/10.3791/63953DOI Listing

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