Abstract
The recent study from the Pogge von Strandmann group published in Cellular and Molecular Immunology, by Alashkar Alhamwe et al., combined for the first time the Cre-LoxP recombination system with single-cell sequencing. The group monitored the tumor-derived extracellular vesicle (EV) uptake and the EV functions in the recipient non-malignant cells in a pancreatic ductal adenocarcinoma mouse model. Recombination events and EV uptake, together with resulting gene expression changes in macrophages, neutrophils, and mast cells, were detected by single-cell sequencing technology of the tumor tissue. This new approach is highly specific, as it can identify single EV recipient cells without interfering with the EV biogenesis or the phenotype.
| Original language | English |
|---|---|
| Pages (from-to) | 714-717 |
| Number of pages | 4 |
| Journal | Extracellular Vesicles and Circulating Nucleic Acids |
| Volume | 5 |
| Issue number | 4 |
| DOIs | |
| State | Published - 2024 |
Keywords
- Bag6
- Cre-LoxP
- Extracellular vesicles
- intracellular cargo transport
- pancreatic ductal adenocarcinoma
- single-cell sequencing
- tumor microenvironments
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