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Mapping human serum-induced gene networks as a basis for the creation of biomimetic periosteum for bone repair.
Al Hosni, Rawiya; Shah, Mittal; Cheema, Umber; Roberts, Helen C; Luyten, Frank P; Roberts, Scott J.
Afiliação
  • Al Hosni R; Department of Materials and Tissue, Institute of Orthopaedics and Musculoskeletal Science, University College London, Stanmore, UK.
  • Shah M; Department of Materials and Tissue, Institute of Orthopaedics and Musculoskeletal Science, University College London, Stanmore, UK.
  • Cheema U; Department of Materials and Tissue, Institute of Orthopaedics and Musculoskeletal Science, University College London, Stanmore, UK.
  • Roberts HC; Department of Natural Sciences, Faculty of Science & Technology, Middlesex University, London, UK.
  • Luyten FP; Skeletal Biology and Tissue Engineering Centre, Department of Development and Regeneration, KU Leuven, Leuven, Belgium and.
  • Roberts SJ; Department of Materials and Tissue, Institute of Orthopaedics and Musculoskeletal Science, University College London, Stanmore, UK; Skeletal Biology and Tissue Engineering Centre, Department of Development and Regeneration, KU Leuven, Leuven, Belgium and; Department of Comparative Biomedical Science
Cytotherapy ; 22(8): 424-435, 2020 08.
Article em En | MEDLINE | ID: mdl-32522398
ABSTRACT

BACKGROUND:

The periosteum is a highly vascularized, collagen-rich tissue that plays a crucial role in directing bone repair. This is orchestrated primarily by its resident progenitor cell population. Indeed, preservation of periosteum integrity is critical for bone healing. Cells extracted from the periosteum retain their osteochondrogenic properties and as such are a promising basis for tissue engineering strategies for the repair of bone defects. However, the culture expansion conditions and the way in which the cells are reintroduced to the defect site are critical aspects of successful translation. Indeed, expansion in human serum and implantation on biomimetic materials has previously been shown to improve in vivo bone formation.

AIM:

This study aimed to develop a protocol to allow for the expansion of human periosteum derived cells (hPDCs) in a biomimetic periosteal-like environment.

METHODS:

The expansion conditions were defined through the investigation of the bioactive cues involved in augmenting hPDC proliferative and multipotency characteristics, based on transcriptomic analysis of cells cultured in human serum.

RESULTS:

Master regulators of transcriptional networks were identified, and an optimized periosteum-derived growth factor cocktail (PD-GFC; containing ß-estradiol, FGF2, TNFα, TGFß, IGF-1 and PDGF-BB) was generated. Expansion of hPDCs in PD-GFC resulted in serum mimicry with regard to the cell morphology, proliferative capacity and chondrogenic differentiation. When incorporated into a three-dimensional collagen type 1 matrix and cultured in PD-GFC, the hPDCs migrated to the surface that represented the matrix topography of the periosteum cambium layer. Furthermore, gene expression analysis revealed a down-regulated WNT and TGFß signature and an up-regulation of CREB, which may indicate the hPDCs are recreating their progenitor cell signature.

CONCLUSION:

This study highlights the first stage in the development of a biomimetic periosteum, which may have applications in bone repair.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Periósteo / Materiais Biomiméticos / Soro / Redes Reguladoras de Genes Tipo de estudo: Prognostic_studies Limite: Adolescent / Animals / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Periósteo / Materiais Biomiméticos / Soro / Redes Reguladoras de Genes Tipo de estudo: Prognostic_studies Limite: Adolescent / Animals / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article