Secreted Particle Information Transfer (SPIT) - A Cellular Platform for In Vivo Genetic Engineering.
Carsten T CharlesworthShota HommaFabian P SuchySicong WangJoydeep BhaduryAnais K AmayaJoab CamarenaJinyu ZhangTze-Kai TanKyomi J IgarashiHiromitsu NakauchiPublished in: bioRxiv : the preprint server for biology (2024)
A multitude of tools now exist that allow us to precisely manipulate the human genome in a myriad of different ways. However, successful delivery of these tools to the cells of human patients remains a major barrier to their clinical implementation. Here we introduce a new cellular approach for in vivo genetic engineering, S ecreted P article I nformation T ransfer (SPIT) that utilizes human cells as delivery vectors for in vivo genetic engineering. We demonstrate the application of SPIT for cell-cell delivery of Cre recombinase and CRISPR-Cas9 enzymes, we show that genetic logic can be incorporated into SPIT and present the first demonstration of human cells as a delivery platform for in vivo genetic engineering in immunocompetent mice. We successfully applied SPIT to genetically modify multiple organs and tissue stem cells in vivo including the liver, spleen, intestines, peripheral blood, and bone marrow. We anticipate that by harnessing the large packaging capacity of a human cell's nucleus, the ability of human cells to engraft into patients' long term and the capacity of human cells for complex genetic programming, that SPIT will become a paradigm shifting approach for in vivo genetic engineering.
Keyphrases
- genome wide
- stem cells
- endothelial cells
- end stage renal disease
- crispr cas
- bone marrow
- copy number
- cell therapy
- single cell
- chronic kidney disease
- healthcare
- induced pluripotent stem cells
- mesenchymal stem cells
- type diabetes
- primary care
- metabolic syndrome
- prognostic factors
- high throughput
- pluripotent stem cells
- cell death
- machine learning
- cell proliferation
- pi k akt
- insulin resistance
- artificial intelligence
- gene therapy
- skeletal muscle
- cell cycle arrest