Hierarchically Structured Biodegradable Microspheres Promote Therapeutic Angiogenesis

Author:

Hendow Eseelle K.1,Iacoviello Francesco2,Casajuana Ester Mar1,Pellet‐Many Caroline3,Day Richard M.1ORCID

Affiliation:

1. Centre for Precision Healthcare UCL Division of Medicine University College London Gower Street London WC1E 6BT UK

2. Electrochemical Innovation Lab UCL Department of Chemical Engineering University College London Roberts Building London WC1E 7JE UK

3. Department of Comparative Biomedical Sciences Royal Veterinary College 4 Royal College Street London NW1 0TU UK

Abstract

AbstractPromoting neovascularization is a prerequisite for many tissue engineering applications and the treatment of cardiovascular disease. Delivery of a pro‐angiogenic stimulus via acellular materials offers several benefits over biological therapies but has been hampered by interaction of the implanted material with the innate immune response. However, macrophages, a key component of the innate immune response, release a plurality of soluble factors that can be harnessed to stimulate neovascularization and restore blood flow to damaged tissue. This study investigates the ability of biodegradable poly(D,L‐lactic‐co‐glycolic acid) (PLGA) microspheres to restore tissue perfusion in a hind limb model of ischaemia. Microspheres exhibiting a hierarchical porous structure are associated with an increase in blood flow at day 21 post‐implantation compared with solid microspheres composed of the same polymer. This corresponds with an increase in blood vessel density in the surrounding tissue. In vitro simulation of the foreign body response observed demonstrates M2‐like macrophages incubated with the porous microspheres secreted increased amounts of vascular endothelial growth factor (VEGF) compared with M1‐like macrophages providing a potential mechanism for the increased neovascularization. The results from this study demonstrate implantable biodegradable porous microspheres provide a novel approach for increasing neovascularization that could be exploited for therapeutic applications.

Funder

British Heart Foundation

UK Research and Innovation

Engineering and Physical Sciences Research Council

Biotechnology and Biological Sciences Research Council

Publisher

Wiley

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