Details
| Originalsprache | Englisch |
|---|---|
| Aufsatznummer | 214413 |
| Fachzeitschrift | Biomaterials Advances |
| Jahrgang | 177 |
| Frühes Online-Datum | 10 Juli 2025 |
| Publikationsstatus | Veröffentlicht - Dez. 2025 |
Abstract
Scaffolds' production for hard to soft tissues recently become of great interest, as bone-tendon insertion tissue engineering, where injuries mainly occur. Interfacial tissue engineering aims at developing grafts to mimic the gradients of those tissues as far as composition, mechanical properties and structures are concerned. Additive manufacturing can offer solutions to meet these requirements, but still requires to improve processes to achieve such gradients in a few steps. In this study, we developed a 3D-printed collector to combine gap-spinning and micropatterning. We were able to manufacture a scaffold (60 mm long, 5 mm wide) with a smooth gradient of 5 mm long from honeycomb structure to aligned fibers (promoting bone and tendon fate, respectively) in a single step. We estimated a gradient in Young modulus from 20 MPa to 30 MPa from the bone to the tendon side. Deformation tracking permitted to highlight significant difference of local strains between both areas, which could then impact cells' response. Murine stem cells C3H10T1/2 were then seeded at both scaffold parts and cultivated without any growth factors in stretching conditions. Alkaline phosphatase staining and tenomodulin immunostaining suggested the effect of stretching to cells' behavior between the bone and tendon area, compared to static condition. However, benefit of topographical and mechanical cues only cannot be fully established to foster cells to specific fate probably due to the limits of this cell line. This novel collector system however permitted to produce a relevant scaffold to study interfaces where a topographical gradient might be needed.
ASJC Scopus Sachgebiete
- Chemische Verfahrenstechnik (insg.)
- Bioengineering
- Werkstoffwissenschaften (insg.)
- Biomaterialien
- Ingenieurwesen (insg.)
- Biomedizintechnik
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in: Biomaterials Advances, Jahrgang 177, 214413, 12.2025.
Publikation: Beitrag in Fachzeitschrift › Artikel › Forschung › Peer-Review
}
TY - JOUR
T1 - Graded electrospun scaffold from aligned fibers to honeycomb micropatterns
T2 - Application to bone-tendon tissue engineering
AU - Rivoallan, Nicolas
AU - Baudequin, Timothée
AU - Mueller, Marc
AU - Nicolas, Rosa
AU - Marin, Sara Leal
AU - Vigneron, Pascale
AU - Jellali, Rachid
AU - Dermigny, Quentin
AU - Le Goff, Anne
AU - Duprez, Delphine
AU - Glasmacher, Birgit
AU - Legallais, Cécile
N1 - Publisher Copyright: © 2025 The Authors
PY - 2025/12
Y1 - 2025/12
N2 - Scaffolds' production for hard to soft tissues recently become of great interest, as bone-tendon insertion tissue engineering, where injuries mainly occur. Interfacial tissue engineering aims at developing grafts to mimic the gradients of those tissues as far as composition, mechanical properties and structures are concerned. Additive manufacturing can offer solutions to meet these requirements, but still requires to improve processes to achieve such gradients in a few steps. In this study, we developed a 3D-printed collector to combine gap-spinning and micropatterning. We were able to manufacture a scaffold (60 mm long, 5 mm wide) with a smooth gradient of 5 mm long from honeycomb structure to aligned fibers (promoting bone and tendon fate, respectively) in a single step. We estimated a gradient in Young modulus from 20 MPa to 30 MPa from the bone to the tendon side. Deformation tracking permitted to highlight significant difference of local strains between both areas, which could then impact cells' response. Murine stem cells C3H10T1/2 were then seeded at both scaffold parts and cultivated without any growth factors in stretching conditions. Alkaline phosphatase staining and tenomodulin immunostaining suggested the effect of stretching to cells' behavior between the bone and tendon area, compared to static condition. However, benefit of topographical and mechanical cues only cannot be fully established to foster cells to specific fate probably due to the limits of this cell line. This novel collector system however permitted to produce a relevant scaffold to study interfaces where a topographical gradient might be needed.
AB - Scaffolds' production for hard to soft tissues recently become of great interest, as bone-tendon insertion tissue engineering, where injuries mainly occur. Interfacial tissue engineering aims at developing grafts to mimic the gradients of those tissues as far as composition, mechanical properties and structures are concerned. Additive manufacturing can offer solutions to meet these requirements, but still requires to improve processes to achieve such gradients in a few steps. In this study, we developed a 3D-printed collector to combine gap-spinning and micropatterning. We were able to manufacture a scaffold (60 mm long, 5 mm wide) with a smooth gradient of 5 mm long from honeycomb structure to aligned fibers (promoting bone and tendon fate, respectively) in a single step. We estimated a gradient in Young modulus from 20 MPa to 30 MPa from the bone to the tendon side. Deformation tracking permitted to highlight significant difference of local strains between both areas, which could then impact cells' response. Murine stem cells C3H10T1/2 were then seeded at both scaffold parts and cultivated without any growth factors in stretching conditions. Alkaline phosphatase staining and tenomodulin immunostaining suggested the effect of stretching to cells' behavior between the bone and tendon area, compared to static condition. However, benefit of topographical and mechanical cues only cannot be fully established to foster cells to specific fate probably due to the limits of this cell line. This novel collector system however permitted to produce a relevant scaffold to study interfaces where a topographical gradient might be needed.
KW - Bone
KW - Electrospinning
KW - Microstructures
KW - Tendon
KW - Tissue engineering
UR - http://www.scopus.com/inward/record.url?scp=105010331601&partnerID=8YFLogxK
U2 - 10.1016/j.bioadv.2025.214413
DO - 10.1016/j.bioadv.2025.214413
M3 - Article
AN - SCOPUS:105010331601
VL - 177
JO - Biomaterials Advances
JF - Biomaterials Advances
SN - 2772-9508
M1 - 214413
ER -