SDF‐1 Bound Heparin Nanoparticles Recruit Progenitor Cells for Their Differentiation and Promotion of Angiogenesis after Stroke

Author:

Wilson Katrina L.1ORCID,Joseph Neica I.1,Onweller Lauren A.1ORCID,Anderson Alexa R.1ORCID,Darling Nicole J.2,David‐Bercholz Jennifer3,Segura Tatiana145ORCID

Affiliation:

1. Department of Biomedical Engineering Duke University Durham NC 27708‐0281 USA

2. Department of Chemical and Biomolecular Engineering University of California Los Angeles Los Angeles CA 90095 USA

3. Department of Anesthesiology Duke University Durham NC 27708‐0281 USA

4. Department of Neurology Duke University Durham NC 27708‐0281 USA

5. Department of Dermatology Duke University Durham NC 27708‐0281 USA

Abstract

AbstractAngiogenesis after stroke is correlated with enhanced tissue repair and functional outcomes. The existing body of research in biomaterials for stroke focuses on hydrogels for the delivery of stem cells, growth factors, or small molecules or drugs. Despite the ability of hydrogels to enhance all these delivery methods, no material has significantly regrown vasculature within the translatable timeline of days to weeks after stroke. Here, two novel biomaterial formulations of granular hydrogels are developed for tissue regeneration after stroke: highly porous microgels (i.e., Cryo microgels) and microgels bound with heparin‐norbornene nanoparticles with covalently bound SDF‐1α. The combination of these materials results in perfused vessels throughout the stroke core in only 10 days, in addition to increased neural progenitor cell recruitment, maintenance, and increased neuronal differentiation.

Funder

National Institutes of Health

National Institute of Neurological Disorders and Stroke

Publisher

Wiley

Subject

Pharmaceutical Science,Biomedical Engineering,Biomaterials

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