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Engineered short forms of perlecan enhance angiogenesis by potentiating growth factor signalling.

Authors :
Kim HN
Elgundi Z
Lin X
Fu L
Tang F
Moh ESX
Jung M
Chandrasekar K
Bartlett-Tomasetig F
Foster C
Packer NH
Whitelock JM
Rnjak-Kovacina J
Lord MS
Source :
Journal of controlled release : official journal of the Controlled Release Society [J Control Release] 2023 Oct; Vol. 362, pp. 184-196. Date of Electronic Publication: 2023 Aug 31.
Publication Year :
2023

Abstract

Growth factors are key molecules involved in angiogenesis, a process critical for tissue repair and regeneration. Despite the potential of growth factor delivery to stimulate angiogenesis, limited clinical success has been achieved with this approach. Growth factors interact with the extracellular matrix (ECM), and particularly heparan sulphate (HS), to bind and potentiate their signalling. Here we show that engineered short forms of perlecan, the major HS proteoglycan of the vascular ECM, bind and signal angiogenic growth factors, including fibroblast growth factor 2 and vascular endothelial growth factor-A. We also show that engineered short forms of perlecan delivered in porous chitosan biomaterial scaffolds promote angiogenesis in a rat full thickness dermal wound model, with the fusion of perlecan domains I and V leading to superior vascularisation compared to native endothelial perlecan or chitosan scaffolds alone. Together, this study demonstrates the potential of engineered short forms of perlecan delivered in chitosan scaffolds as next generation angiogenic therapies which exert biological activity via the potentiation of growth factors.<br />Competing Interests: Declaration of Competing Interest The authors declare no competing interest.<br /> (Copyright © 2023 The Author(s). Published by Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1873-4995
Volume :
362
Database :
MEDLINE
Journal :
Journal of controlled release : official journal of the Controlled Release Society
Publication Type :
Academic Journal
Accession number :
37648081
Full Text :
https://doi.org/10.1016/j.jconrel.2023.08.052