Metadata
Title
Leveraging viscosity to unlock the osteogenic potential of BMP-2 mimetic DWIVA
Category
general
UUID
875459de115b4143a8f0191daa068c70
Source URL
https://eprints.gla.ac.uk/374897/
Parent URL
https://eprints.gla.ac.uk/view/project_code/303613.html
Crawl Time
2026-03-11T05:45:05+00:00
Rendered Raw Markdown

Leveraging viscosity to unlock the osteogenic potential of BMP-2 mimetic DWIVA

Source: https://eprints.gla.ac.uk/374897/ Parent: https://eprints.gla.ac.uk/view/project_code/303613.html

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Leveraging viscosity to unlock the osteogenic potential of BMP-2 mimetic DWIVA

Cunniffe, Finlay, Luo, Ziyuan, Barcelona-Estaje, Eva, Forrest, Eva, Salmeron-Sanchez, Manuel ORCID: https://orcid.org/0000-0002-8112-2100 and Cantini, Marco ORCID: https://orcid.org/0000-0003-0326-1508 (2025) Leveraging viscosity to unlock the osteogenic potential of BMP-2 mimetic DWIVA. Small, (doi: 10.1002/smll.202508366) (PMID:41469973)

(Early Online Publication)

Text 374897.pdf - Published Version Available under License Creative Commons Attribution. 5MB

Abstract

Growth factor mimetics offer great potential for osteogenic biomaterials; yet, their use remains limited, likely due to an incomplete understanding of the effects of the microenvironment on their activity. The extracellular matrices (ECMs) where growth factors are presented in vivo are viscoelastic environments, where dynamic receptor-ligand interactions drive cellular responses. Here, supported lipid bilayers of varying viscosity are used as 2D dynamic ECM models, where the bone morphogenetic 2 (BMP-2) mimetic DWIVA is presented to mesenchymal stem cells alongside the adhesive peptide RGD. DWIVA is demonstrated to have no impact on mechanotransductive processes, including actin organisation, focal adhesion formation and YAP localisation, which are exclusively controlled by viscosity via RGD. Interestingly, DWIVA promotes osteogenic markers’ expression only on a viscous bilayer, through a process that involves non-canonical BMP-2 pathways; on a mobile bilayer or on a static control, it lacks osteogenic activity. Crucially, osteogenesis is accompanied by a translocation of BMP receptor 1a to the cell edge, where it colocalises with focal adhesions. Our ECM models hence reveal that both a viscosity-enabled threshold of cell-generated forces and a dynamic environment are necessary to harness the osteogenic potential of DWIVA, uncovering key microenvironment properties for the design of DWIVA-based biomaterials.

Item Type: Articles
Additional Information: MC acknowledges support from The Medical Research Council (MR/S005412/1), The Royal Society (RGS/R1/231400), and The Carnegie Trust for the Universities of Scotland (RIG013300). M.S-S is funded by the European Union’s Horizon 2020 research and innovation programme (Grant agreement No. 874889 - HEALIKICK), European Research Council AdG (101054728) and EPSRC through the Transformative Healthcare Technologies Programme Grant ‘Mechanomeds’ (EP/X033554/1). IBEC is a recipient of a Severo Ochoa Award of Excellence from MINCIN and member of CERCA Programme / Generalitat de Catalunya.
Keywords: Viscosity, BMP-2, DWIVA, mesenchymal stem cell, osteogenesis.
Status: Early Online Publication
Refereed: Yes
Glasgow Author(s) Enlighten ID: Cantini, Dr Marco and Barcelona Estaje, Eva and Cunniffe, Finlay and Salmeron-Sanchez, Professor Manuel and Luo, Ziyuan
Authors: Cunniffe, F., Luo, Z., Barcelona-Estaje, E., Forrest, E., Salmeron-Sanchez, M., and Cantini, M.
College/School: College of Science and Engineering > School of Engineering > Biomedical Engineering
Journal Name: Small
Publisher: Wiley
ISSN: 1613-6810
ISSN (Online): 1613-6829
Published Online: 30 December 2025
Copyright Holders: Copyright © 2025 The Author(s)
First Published: First published in Small 2025
Publisher Policy: Reproduced under a Creative Commons license

University Staff: Request a correction | Enlighten Editors: Update this record

Funder and Project Information

Funder and Project Information

Funder and Project Information

Project Code

Award No

Project Name

Principal Investigator

Funder's Name

Funder Ref

Lead Dept

303613

Engineered microenvironments to harvest stem cell response to viscosity for cartilage repair

Marco Cantini

Medical Research Council (MRC)

MR/S005412/1

ENG - Biomedical Engineering

320080

Harnessing viscoelasticity for regenerative medicine

Marco Cantini

The Royal Society (ROYSOC)

RGS/R1/231400

ENG - Biomedical Engineering

324055

Viscoelastic regulation of growth factor activity

Marco Cantini

The Carnegie Trust for the Universities of Scotland (CARNEGTR)

RIG013300

ENG - Biomedical Engineering

307621

HEALIKICK

Manuel Salmeron-Sanchez

European Commission (EC)

874889

School of Molecular Biosciences

315918

DEVISE - Engineered viscoelasticity in regenerative microenvironments

Manuel Salmeron-Sanchez

EPSRC EU Guarantee (EPSRCEU)

101054728

ENG - Biomedical Engineering

318950

Mechanobiology-based medicine - Phase 2

Manuel Salmeron-Sanchez

Engineering and Physical Sciences Research Council (EPSRC)

EP/X033554/1

ENG - Biomedical Engineering

Deposit and Record Details

Deposit and Record Details

Deposit and Record Details

ID Code: 374897
Depositing User: Mr Alastair Arthur
Datestamp: 19 Dec 2025 15:26
Last Modified: 09 Jan 2026 10:28
Date of acceptance: 19 December 2025
Date of first online publication: 30 December 2025
Date Deposited: 19 December 2025
Data Availability Statement: No

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