Transcriptional Engineering of Hematopoietic Stem Cells using CRISPR

Informacje na temat projektu

HSC-CRISPR

Identyfikator umowy o grant: 101041231

DOI

10.3030/101041231

Data podpisania przez KE 14 Lutego 2022

Data rozpoczęcia 1 Września 2022

Data zakończenia 31 Sierpnia 2027

Finansowanie w ramach

• European Research Council (ERC)

Koszt całkowity

€ 1 499 923,00

Wkład UE

€ 1 499 923,00

Koordynowany przez

AARHUS UNIVERSITET
Denmark

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

Okres sprawozdawczy: 2022-09-01 do 2025-02-28

Podsumowanie kontekstu i ogólnych celów projektu

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.

Prace wykonane od początku projektu do końca okresu sprawozdawczego oraz najważniejsze dotychczasowe rezultaty

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.

Innowacyjność oraz oczekiwany potencjalny wpływ (w tym dotychczasowe znaczenie społeczno-gospodarcze i szersze implikacje społeczne projektu)

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.