fig1

Evaluating different routes of extracellular vesicle administration for cranial therapies

Figure 1. In vivo tracking of extracellular vesicles (EV) in the prefrontal cortex and subventricular zone after intracranial (IC), retro-orbital (RO), or intranasal (IN) injections. hNSC-derived-EV labeled with fluorescent dye were transplanted using stereotaxic IC (A, D), RO (B, E), or IN (C, F) injections. The brain tissues were fixed at 48 h post-surgery and sections imaged using confocal microscopy. Confocal Z-stacks were collected at 60 × magnification and qualitatively demonstrate that injected EV (red, DAPI nuclear counterstain, blue) migrated to the pre-limbic (PRL) and infra (IL) limbic structures of the PFC (A-C) and the SVZ (D-F). Magnified images (a1-f1) demonstrate localization of EV in close vicinity of the cell bodies after IC, RO, and IN administration. Scale bars: 20 µm (A-F) and 3 µm (a1-f1)

Journal of Cancer Metastasis and Treatment
ISSN 2454-2857 (Online) 2394-4722 (Print)

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