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Active NON-SBIR/STTR RPGS NIH (US)

Cell-drones: engineered stem cell nanovesicles as alternatives to exosomes

$4.03M USD

Funder NATIONAL HEART, LUNG, AND BLOOD INSTITUTE
Recipient Organization Columbia University New York Morningside
Country United States
Start Date Sep 01, 2024
End Date Aug 31, 2028
Duration 1,460 days
Number of Grantees 1
Roles Principal Investigator
Data Source NIH (US)
Grant ID 10943490
Grant Description

PROJECT SUMMARY Studies have demonstrated that adult stem cells such as mesenchymal stem cells (MSCs) repair myocardial infarction (MI) or ischemia/reperfusion (I/R) injury by indirect paracrine mechanisms rather than by differentiation and tissue replacement. In the past decade, extracellular vesicles (EVs) have emerged as

promising cell-free agents for treating ischemic injury. Several exosome-based therapeutic companies have launched early phase clinical trials. However, the large-scale production of EVs remains a challenge. We seek to develop a scale-up friendly method to generate a large number of therapeutic nanovesicles (NVs) from

MSCs by extrusion. Passing through a series of extrusion microfilters, the MSCs can be converted into billions of NVs. Those engineered cell vesicles serve as “cell-drones” to deliver biological information to the recipient cells. Companies such as MDImune and SQZ Biotech are conducting clinical trials using extruded

nanovesicles in the area of oncology and infectious diseases. We wonder whether those cell-drones would carry the regenerative materials from MSCs and can promote tissue repair in a way similar or superior to naturally secreted EVs. In this proposed study, we plan to investigate the fabrication, characterization and

toxicity of NVs (Preliminary study). After that, we will test the therapeutic effect of NVs on a mouse model (AIM 1) and a porcine model (AIM 2) with cardiac I/R injury. Then, we will elucidate the mechanisms underlying the therapeutic benefits of MSC NVs and create “super” NVs with enhancement cargos (AIM 3). This leads to our

central hypothesis that extrusion is a highly efficient method to generate a large quantity of therapeutic NVs that can potentially be manipulated, and may replace EVs in regenerative medicine applications.

All Grantees

Columbia University New York Morningside

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