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Tissue constructs with human adipose-derived mesenchymal stem cells to treat bone defects in rats

Tissue constructs with human adipose-derived mesenchymal stem cells to treat bone defects in rats
Tissue constructs with human adipose-derived mesenchymal stem cells to treat bone defects in rats
The use of porous scaffolds created by additive manufacturing is considered a viable approach for the regeneration of critical-size bone defects. This paper investigates the xenotransplantation of polycaprolactone (PCL) tissue constructs seeded with differentiated and undifferentiated human adipose-derived mesenchymal stem cells (hADSCs) to treat calvarial critical-sized defect in Wistar rats. PCL scaffolds without cells were also considered. In vitro and in vivo biological evaluations were performed to assess the feasibility of these different approaches. In the case of cell seeded scaffolds, it was possible to observe the presence of hADSCs in the rat tissue contributing directly (osteoblasts) and indirectly (stimulation by paracrine factors) to tissue formation, organization and mineralization. The presence of bone morphogenetic protein-2 (BMP-2) in the rat tissue treated with cell-seeded PCL scaffolds suggests that the paracrine factors of undifferentiated hADSC cells could stimulate BMP-2 production by surrounding cells, leading to osteogenesis. Moreover, BMP-2 acts synergistically with growth factors to induce angiogenesis, leading to higher numbers of blood vessels in the groups containing undifferentiated and differentiated hADSCs.
Caetano, G.
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Wang, W.
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Murashima, A.
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Jr, J.R. Passarini
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Bagne, L.
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Leite, M
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Hyppolito, M.
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Al-Deyab, S.
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El-Newehy, M.
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Bartolo, Paulo Jorge Da Silva
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Frade, M.A.C.
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Caetano, G.
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Wang, W.
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Murashima, A.
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Jr, J.R. Passarini
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Bagne, L.
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Leite, M
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Hyppolito, M.
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Al-Deyab, S.
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El-Newehy, M.
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Bartolo, Paulo Jorge Da Silva
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Frade, M.A.C.
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Caetano, G., Wang, W., Murashima, A., Jr, J.R. Passarini, Bagne, L., Leite, M, Hyppolito, M., Al-Deyab, S., El-Newehy, M., Bartolo, Paulo Jorge Da Silva and Frade, M.A.C. (2019) Tissue constructs with human adipose-derived mesenchymal stem cells to treat bone defects in rats. Materials, 12 (14). (doi:10.3390/ma12142268).

Record type: Article

Abstract

The use of porous scaffolds created by additive manufacturing is considered a viable approach for the regeneration of critical-size bone defects. This paper investigates the xenotransplantation of polycaprolactone (PCL) tissue constructs seeded with differentiated and undifferentiated human adipose-derived mesenchymal stem cells (hADSCs) to treat calvarial critical-sized defect in Wistar rats. PCL scaffolds without cells were also considered. In vitro and in vivo biological evaluations were performed to assess the feasibility of these different approaches. In the case of cell seeded scaffolds, it was possible to observe the presence of hADSCs in the rat tissue contributing directly (osteoblasts) and indirectly (stimulation by paracrine factors) to tissue formation, organization and mineralization. The presence of bone morphogenetic protein-2 (BMP-2) in the rat tissue treated with cell-seeded PCL scaffolds suggests that the paracrine factors of undifferentiated hADSC cells could stimulate BMP-2 production by surrounding cells, leading to osteogenesis. Moreover, BMP-2 acts synergistically with growth factors to induce angiogenesis, leading to higher numbers of blood vessels in the groups containing undifferentiated and differentiated hADSCs.

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materials-12-02268 - Version of Record
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Accepted/In Press date: 11 July 2019
Published date: 15 July 2019

Identifiers

Local EPrints ID: 503882
URI: http://eprints.soton.ac.uk/id/eprint/503882
PURE UUID: 779ef1e2-1bf3-4251-9518-a78064be7152
ORCID for W. Wang: ORCID iD orcid.org/0000-0002-8959-329X

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Date deposited: 15 Aug 2025 16:46
Last modified: 22 Aug 2025 02:46

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Contributors

Author: G. Caetano
Author: W. Wang ORCID iD
Author: A. Murashima
Author: J.R. Passarini Jr
Author: L. Bagne
Author: M Leite
Author: M. Hyppolito
Author: S. Al-Deyab
Author: M. El-Newehy
Author: Paulo Jorge Da Silva Bartolo
Author: M.A.C. Frade

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