Combining Cre-LoxP and single-cell sequencing technologies: insights into the extracellular vesicle cargo transfer.

Extracellular vesicles and circulating nucleic acids Pub Date : 2024-11-09 eCollection Date: 2024-01-01 DOI:10.20517/evcna.2024.58
Michael W Pfaffl
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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.

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结合Cre-LoxP和单细胞测序技术:洞察细胞外囊泡货物转移。
最近由Alashkar Alhamwe等人发表在《细胞与分子免疫学》上的Pogge von Strandmann小组的研究首次将Cre-LoxP重组系统与单细胞测序结合起来。在胰腺导管腺癌小鼠模型中,研究小组监测了受体非恶性细胞的肿瘤源性细胞外囊泡(EV)摄取和EV功能。通过肿瘤组织单细胞测序技术检测巨噬细胞、中性粒细胞和肥大细胞中重组事件和EV摄取以及由此产生的基因表达变化。这种新方法具有很高的特异性,因为它可以识别单个EV受体细胞,而不会干扰EV的生物发生或表型。
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