Transcriptional Engineering of Hematopoietic Stem Cells using CRISPR

Informazioni relative al progetto

HSC-CRISPR

ID dell’accordo di sovvenzione: 101041231

DOI

10.3030/101041231

Data della firma CE 14 Febbraio 2022

Data di avvio 1 Settembre 2022

Data di completamento 31 Agosto 2027

Finanziato da

• European Research Council (ERC)

Costo totale

€ 1 499 923,00

Contributo UE

€ 1 499 923,00

Coordinato da

AARHUS UNIVERSITET
Denmark

Periodic Reporting for period 1 - HSC-CRISPR (Transcriptional Engineering of Hematopoietic Stem Cells using CRISPR)

Periodo di rendicontazione: 2022-09-01 al 2025-02-28

Sintesi del contesto e degli obiettivi generali del progetto

This project revolves around the ability to modify the transcriptome of hematopoietic stem cells to enhance their therapeutic potential. These cells are used for transplantation purposes as they possess the ability to repopulate the blood and immune system for the life time of a patient. They are therefore used to treat people with genetic blood disorders or blood cancers. The challenges with these cells are mainly associated with their scarcity and the insusceptibility to precise genetic therapy in these cells. The overall objective is to use CRISPR/Cas-based tools to transcriptionally engineer these cells to enhance their properties in regards to these challenges.

Lavoro eseguito dall’inizio del progetto fino alla fine del periodo coperto dalla relazione e principali risultati finora ottenuti

We have performed work related to bringing RNA-based delivery approaches of CRISPR activation (CRISPRa) and CRISPR interference (CRISPRi) into clinically relevant primary cells including CD34+ hematopoietic stem cells. We have tested different transcriptional effector domains and different Cas orthologs and identified combinations that work efficiently and that enable orthogonal and multiplexed transcriptional regulation where one set of genes is upregulated and another set is downregulated following a single delivery of relevant RNA-based reagents (mRNA + sgRNAs). In addition, we have shown that we can combine this with a third Cas ortholog to enable trimodal engineering where, in addition to orthogonal transcriptional engineering, we have also included gene editing in the form of gene knockout. Additionally, we have also identified new ways of tuning transcriptional efficiency so this gene modulation effect can be tuned to a desirable level. Finally, we have identified a potential major restriction factor for AAV transduction in CD34+ hematopoietic stem cells, which we must still explore to identify its importance in genetic engineering using HDR-based CRISPR/Cas editing using AAV6 as HDR repair template.

Progressi oltre lo stato dell’arte e potenziale impatto previsto (incluso l’impatto socioeconomico e le implicazioni sociali più ampie del progetto fino ad ora)

Trimodal engineering and tunable transcriptional engineering represent novel approaches to genetically manipulate cells in a sophisticated way. We believe that complex genetic engineering can find use in many avenues of cell and gene therapies. The CRISPRa and CRISPRi tools have previously not found much application in therapy, but our findings pave the way for such use. HDR-based gene correction or insertion is the most flexible way of performing gene editing in human cells but is restricted in efficiency. With the hypothesis that AAV6 HDR repair template delivery and nuclear availability is a major bottleneck in the HDR process, the identification of a major restriction factor to this might enable wide-spread therapeutic use in CD34+ hematopoietic stem cells and benefit major patient populations with diseases in the blood and immune system.