Literature DB >> 26840227

Delivery of Genome Editing Reagents to Hematopoietic Stem/Progenitor Cells.

Megan D Hoban1, Zulema Romero1, Gregory J Cost2, Matthew Mendel2, Michael Holmes2, Donald B Kohn1,3.   

Abstract

This unit describes the protocol for the delivery of reagents for targeted genome editing to CD34(+) hematopoietic stem/progenitor cells (HSPCs). Specifically, this unit focuses on the process of thawing and pre-stimulating CD34(+) HSPCs, as well as the details of their electroporation with in vitro-transcribed mRNA-encoding site-specific nucleases [in this case zinc-finger nucleases (ZFNs)]. In addition, discussed is delivery of a gene editing donor template in the form of an oligonucleotide or integrase-defective lentiviral vector (IDLV). Finally, an analysis of cell survival following treatment and downstream culture conditions are presented. While optimization steps might be needed for each specific application with respect to nuclease and donor template amount, adherence to this protocol will serve as an excellent starting point for this further work.
Copyright © 2016 John Wiley & Sons, Inc.

Entities:  

Keywords:  electroporation; genome editing; hematopoietic stem cells; targeted nucleases

Mesh:

Substances:

Year:  2016        PMID: 26840227     DOI: 10.1002/9780470151808.sc05b04s36

Source DB:  PubMed          Journal:  Curr Protoc Stem Cell Biol        ISSN: 1938-8969


  5 in total

1.  A Protocol for the Production of Integrase-deficient Lentiviral Vectors for CRISPR/Cas9-mediated Gene Knockout in Dividing Cells.

Authors:  Sriram Vijayraghavan; Boris Kantor
Journal:  J Vis Exp       Date:  2017-12-12       Impact factor: 1.355

2.  Adeno-Associated Virus and Hematopoietic Stem Cells: The Potential of Adeno-Associated Virus Hematopoietic Stem Cells in Genetic Medicines.

Authors:  Saswati Chatterjee; Venkatesh Sivanandam; Kamehameha Kai-Min Wong
Journal:  Hum Gene Ther       Date:  2020-05       Impact factor: 5.695

3.  CRISPR/Cas9-Mediated Correction of the Sickle Mutation in Human CD34+ cells.

Authors:  Megan D Hoban; Dianne Lumaquin; Caroline Y Kuo; Zulema Romero; Joseph Long; Michelle Ho; Courtney S Young; Michelle Mojadidi; Sorel Fitz-Gibbon; Aaron R Cooper; Georgia R Lill; Fabrizia Urbinati; Beatriz Campo-Fernandez; Carmen F Bjurstrom; Matteo Pellegrini; Roger P Hollis; Donald B Kohn
Journal:  Mol Ther       Date:  2016-07-29       Impact factor: 11.454

4.  Enhancement of mouse hematopoietic stem/progenitor cell function via transient gene delivery using integration-deficient lentiviral vectors.

Authors:  Maria E Alonso-Ferrero; Niek P van Til; Kerol Bartolovic; Márcia F Mata; Gerard Wagemaker; Dale Moulding; David A Williams; Christine Kinnon; Simon N Waddington; Michael D Milsom; Steven J Howe
Journal:  Exp Hematol       Date:  2017-09-11       Impact factor: 3.084

5.  Integrase-Deficient Lentiviral Vector as an All-in-One Platform for Highly Efficient CRISPR/Cas9-Mediated Gene Editing.

Authors:  Pavel I Ortinski; Bernadette O'Donovan; Xiaoyu Dong; Boris Kantor
Journal:  Mol Ther Methods Clin Dev       Date:  2017-04-19       Impact factor: 6.698

  5 in total

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