Syndecan-4 proteoliposomes enhance revascularization in a rabbit hind limb ischemia model of peripheral ischemia.

Alginate Critical limb ischemia Fibroblast growth factor-2 Intermittent claudication Peripheral ischemia Peripheral vascular disease Platelet derived growth factor-BB Revascularization Syndecan-4 proteoliposomes Therapeutic angiogenesis

Journal

Acta biomaterialia
ISSN: 1878-7568
Titre abrégé: Acta Biomater
Pays: England
ID NLM: 101233144

Informations de publication

Date de publication:
01 09 2023
Historique:
received: 04 10 2022
revised: 07 06 2023
accepted: 08 06 2023
medline: 31 7 2023
pubmed: 16 6 2023
entrez: 15 6 2023
Statut: ppublish

Résumé

Regenerative therapeutics for treating peripheral arterial disease are an appealing strategy for creating more durable solutions for limb ischemia. In this work, we performed preclinical testing of an injectable formulation of syndecan-4 proteoliposomes combined with growth factors as treatment for peripheral ischemia delivered in an alginate hydrogel. We tested this therapy in an advanced model of hindlimb ischemia in rabbits with diabetes and hyperlipidemia. Our studies demonstrate enhancement in vascularity and new blood vessel growth with treatment with syndecan-4 proteoliposomes in combination with FGF-2 or FGF-2/PDGF-BB. The effects of the treatments were particularly effective in enhancing vascularity in the lower limb with a 2-4 increase in blood vessels in the treatment group in comparison to the control group. In addition, we demonstrate that the syndecan-4 proteoliposomes have stability for at least 28 days when stored at 4°C to allow transport and use in the hospital environment. In addition, we performed toxicity studies in the mice and found no toxic effects even when injected at high concentration. Overall, our studies support that syndecan-4 proteoliposomes markedly enhance the therapeutic potential of growth factors in the context of disease and may be promising therapeutics for inducing vascular regeneration in peripheral ischemia. STATEMENT OF SIGNIFICANCE: Peripheral ischemia is a common condition in which there is a lack of blood flow to the lower limbs. This condition can lead to pain while walking and, in severe cases, critical limb ischemia and limb loss. In this study, we demonstrate the safety and efficacy of a novel injectable therapy for enhancing revascularization in peripheral ischemia using an advanced large animal model of peripheral vascular disease using rabbits with hyperlipidemia and diabetes.

Identifiants

pubmed: 37321528
pii: S1742-7061(23)00331-8
doi: 10.1016/j.actbio.2023.06.006
pii:
doi:

Substances chimiques

proteoliposomes 0
Syndecan-4 0
Fibroblast Growth Factor 2 103107-01-3

Types de publication

Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

425-435

Informations de copyright

Copyright © 2023 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: The senior author (ABB) has a US patent on the technology in this manuscript.

Auteurs

Andrew D Sligar (AD)

Department of Biomedical Engineering, University of Texas at Austin, 1 University Station, BME 5.202D, C0800, Austin, TX 78712, USA.

Gretchen Howe (G)

Division of Cardiovascular Medicine, Department of Internal Medicine, University of Texas Medical School at Houston, TX, USA.

Julia Goldman (J)

Center for Laboratory Animal Medicine and Care, UT Health Science Center at Houston, USA.

Patricia Felli (P)

Division of Cardiovascular Medicine, Department of Internal Medicine, University of Texas Medical School at Houston, TX, USA.

Almudena Gómez-Hernández (A)

Department of Biochemistry and Molecular Biology, School of Pharmacy, Complutense University of Madrid, Madrid, Spain.

Eri Takematsu (E)

Department of Biomedical Engineering, University of Texas at Austin, 1 University Station, BME 5.202D, C0800, Austin, TX 78712, USA.

Austin Veith (A)

Department of Biomedical Engineering, University of Texas at Austin, 1 University Station, BME 5.202D, C0800, Austin, TX 78712, USA.

Shubh Desai (S)

Department of Biomedical Engineering, University of Texas at Austin, 1 University Station, BME 5.202D, C0800, Austin, TX 78712, USA.

William J Riley (WJ)

Department of Biomedical Engineering, University of Texas at Austin, 1 University Station, BME 5.202D, C0800, Austin, TX 78712, USA.

Rohan Singeetham (R)

Department of Biomedical Engineering, University of Texas at Austin, 1 University Station, BME 5.202D, C0800, Austin, TX 78712, USA.

Lei Mei (L)

Department of Biomedical Engineering, University of Texas at Austin, 1 University Station, BME 5.202D, C0800, Austin, TX 78712, USA.

Gregory Callahan (G)

Department of Biomedical Engineering, University of Texas at Austin, 1 University Station, BME 5.202D, C0800, Austin, TX 78712, USA.

David Ashirov (D)

Department of Biomedical Engineering, University of Texas at Austin, 1 University Station, BME 5.202D, C0800, Austin, TX 78712, USA.

Richard Smalling (R)

Division of Cardiovascular Medicine, Department of Internal Medicine, University of Texas Medical School at Houston, TX, USA; Memorial Hermann Heart and Vascular Institute, Houston, TX, USA.

Aaron B Baker (AB)

Department of Biomedical Engineering, University of Texas at Austin, 1 University Station, BME 5.202D, C0800, Austin, TX 78712, USA; Institute for Cellular and Molecular Biology, University of Texas at Austin, Austin, TX, USA; The Institute for Computational Engineering and Sciences, University of Texas at Austin, Austin, TX, USA; Institute for Biomaterials, Drug Delivery and Regenerative Medicine, University of Texas at Austin, Austin, TX, USA. Electronic address: abbaker@austin.utexas.edu.

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Classifications MeSH