Food, Microbiome and Health Research Programme, Quadram Institute Bioscience, Norwich, UK.
Norwich Medical School, University of East Anglia, Norwich, UK.
Methods Mol Biol. 2024;2843:239-251. doi: 10.1007/978-1-0716-4055-5_15.
Bacterial extracellular vesicles (BEVs) are nano-size vesicles containing a cargo of bioactive molecules that can play key roles in microbe-microbe and microbe-host interactions. In tracking their biodistribution in vivo, BEVs can cross several physical host barriers including the intestinal epithelium, vascular endothelium, and blood-brain-barrier (BBB) to ultimately accumulate in tissues such as the liver, lungs, spleen, and the brain. This tissue-specific dissemination has been exploited for the delivery of biomolecules such as vaccines for mucosal delivery. Although numerous strategies for labeling and tracking BEVs have been described, most have constraints that impact on interpreting in vivo bioimaging patterns. Here, we describe a general method for labeling BEVs using lipophilic fluorescent membrane stains which can be adopted by non-expert users. We also describe how the procedure can be used to overcome potential limitations. Furthermore, we outline methods of quantitative ex vivo tissue imaging that can be used to evaluate BEV organ trafficking.
细菌细胞外囊泡(BEVs)是纳米大小的囊泡,其中包含生物活性分子的货物,这些分子在微生物-微生物和微生物-宿主相互作用中起着关键作用。在跟踪其体内的生物分布时,BEVs 可以穿过几个物理宿主屏障,包括肠道上皮、血管内皮和血脑屏障(BBB),最终积累在肝脏、肺部、脾脏和大脑等组织中。这种组织特异性的传播已被用于输送生物分子,如用于粘膜输送的疫苗。尽管已经描述了许多标记和跟踪 BEVs 的策略,但大多数策略都存在影响体内生物成像模式解释的限制。在这里,我们描述了一种使用亲脂性荧光膜染料标记 BEVs 的通用方法,非专业用户也可以采用该方法。我们还描述了如何使用该程序来克服潜在的限制。此外,我们概述了可用于评估 BEV 器官贩运的定量离体组织成像方法。