Sustained Knockdown of a Disease‐Causing Gene in Patient‐Specific Induced Pluripotent Stem Cells Using Lentiviral Vector‐Based Gene Therapy

• Published in: Stem cells translational medicine Vol. 2; no. 9; pp. 641 - 654
• Main Authors: Eggenschwiler, Reto, Loya, Komal, Wu, Guangming, Sharma, Amar Deep, Sgodda, Malte, Zychlinski, Daniela, Herr, Christian, Steinemann, Doris, Teckman, Jeffrey, Bals, Robert, Ott, Michael, Schambach, Axel, Schöler, Hans Robert, Cantz, Tobias
• Format: Journal Article
• Language: English
• Published: United States AlphaMed Press 01.09.2013; Oxford University Press
• Subjects: alpha 1-Antitrypsin - genetics; alpha 1-Antitrypsin - metabolism; alpha 1-Antitrypsin Deficiency - genetics; alpha 1-Antitrypsin Deficiency - metabolism; alpha 1-Antitrypsin Deficiency - therapy; Animals; Cell Differentiation; Cells, Cultured; Clinical trials; Data analysis; Embryonic Stem Cells/Induced Pluripotent Stem (iPS) Cells; Expression vectors; Gene Knockdown Techniques - methods; Gene therapy; Genetic disorders; Genetic Therapy - methods; Genetic Vectors; Genomes; Green Fluorescent Proteins - genetics; Hepatocyte differentiation; Hepatocytes - cytology; Hepatocytes - metabolism; Hepatocytes - virology; Humans; Induced Pluripotent Stem Cells - cytology; Induced Pluripotent Stem Cells - metabolism; Induced Pluripotent Stem Cells - virology; Laboratories; Lentiviral vector; Lentivirus - genetics; Liver; Liver diseases; Mice; Mice, Transgenic; MicroRNAs - genetics; Pluripotency; Pluripotent stem cells; Promoter Regions, Genetic; Proteins; Ribonucleic acid; RNA; RNA Polymerase II - genetics; RNA, Small Interfering - genetics; RNAi; Stem cells; Transgenes; Vectors (Biology); Lentiviral vector; RNAi; Hepatocyte differentiation; Gene therapy; Pluripotent stem cells; Liver
• ISSN: 2157-6564; 2157-6580
• DOI: 10.5966/sctm.2013-0017

This study proposes an approach for the expression of a therapeutic short hairpin RNA (shRNA) in disease‐specific induced pluripotent stem cells (iPSCs) using third‐generation lentiviral vectors. It was found that lentiviral vector‐mediated expression of shRNAs can be efficiently used to knock down and functionally evaluate disease‐related genes in patient‐specific iPSCs. Patient‐specific induced pluripotent stem cells (iPSCs) hold great promise for studies on disease‐related developmental processes and may serve as an autologous cell source for future treatment of many hereditary diseases. New genetic engineering tools such as zinc finger nucleases and transcription activator‐like effector nuclease allow targeted correction of monogenetic disorders but are very cumbersome to establish. Aiming at studies on the knockdown of a disease‐causing gene, lentiviral vector‐mediated expression of short hairpin RNAs (shRNAs) is a valuable option, but it is limited by silencing of the knockdown construct upon epigenetic remodeling during differentiation. Here, we propose an approach for the expression of a therapeutic shRNA in disease‐specific iPSCs using third‐generation lentiviral vectors. Targeting severe α‐1‐antitrypsin (A1AT) deficiency, we overexpressed a human microRNA 30 (miR30)‐styled shRNA directed against the PiZ variant of A1AT, which is known to cause chronic liver damage in affected patients. This knockdown cassette is traceable from clonal iPSC lines to differentiated hepatic progeny via an enhanced green fluorescence protein reporter expressed from the same RNA‐polymerase II promoter. Importantly, the cytomegalovirus i/e enhancer chicken β actin (CAG) promoter‐driven expression of this construct is sustained without transgene silencing during hepatic differentiation in vitro and in vivo. At low lentiviral copy numbers per genome we confirmed a functional relevant reduction (−66%) of intracellular PiZ protein in hepatic cells after differentiation of patient‐specific iPSCs. In conclusion, we have demonstrated that lentiviral vector‐mediated expression of shRNAs can be efficiently used to knock down and functionally evaluate disease‐related genes in patient‐specific iPSCs.