Tracking Radiolabeled Endothelial Microvesicles Predicts Their Therapeutic Efficacy: A Proof-of-Concept Study in Peripheral Ischemia Mouse Model Using SPECT/CT Imaging

Microvesicles, so-called endothelial large extracellular vesicles (LEVs), are of great interest as biological markers and cell-free biotherapies in cardiovascular and oncologic diseases. However, their therapeutic perspectives remain limited due to the lack of reliable data regarding their systemic...

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Main Authors: Romain Giraud (Author), Anaïs Moyon (Author), Stéphanie Simoncini (Author), Anne-Claire Duchez (Author), Vincent Nail (Author), Corinne Chareyre (Author), Ahlem Bouhlel (Author), Laure Balasse (Author), Samantha Fernandez (Author), Loris Vallier (Author), Guillaume Hache (Author), Florence Sabatier (Author), Françoise Dignat-George (Author), Romaric Lacroix (Author), Benjamin Guillet (Author), Philippe Garrigue (Author)
Format: Book
Published: MDPI AG, 2022-01-01T00:00:00Z.
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Summary:Microvesicles, so-called endothelial large extracellular vesicles (LEVs), are of great interest as biological markers and cell-free biotherapies in cardiovascular and oncologic diseases. However, their therapeutic perspectives remain limited due to the lack of reliable data regarding their systemic biodistribution after intravenous administration. Methods: Applied to a mouse model of peripheral ischemia, radiolabeled endothelial LEVs were tracked and their in vivo whole-body distribution was quantified by microSPECT/CT imaging. Hindlimb perfusion was followed by LASER Doppler and motility impairment function was evaluated up to day 28 post-ischemia. Results: Early and specific homing of LEVs to ischemic hind limbs was quantified on the day of ischemia and positively correlated with reperfusion intensity at a later stage on day 28 after ischemia, associated with an improved motility function. Conclusions: This concept is a major asset for investigating the biodistribution of LEVs issued from other cell types, including cancer, thus partly contributing to better knowledge and understanding of their fate after injection.
Item Description:10.3390/pharmaceutics14010121
1999-4923