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Orthotopic Bone Formation by Streamlined Engineering and Devitalization of Human Hypertrophic Cartilage

Pigeot, Sébastien (author)
University Hospital Basel
Bourgine, Paul Emile (author)
Lund University,Lunds universitet,Molekylär skelettbiologi,Forskargrupper vid Lunds universitet,WCMM- Wallenberg center för molekylär medicinsk forskning,Medicinska fakulteten,Molecular Skeletal Biology,Lund University Research Groups,WCMM-Wallenberg Centre for Molecular Medicine,Faculty of Medicine,University Hospital Basel
Claude, Jaquiery (author)
University Hospital Basel
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Scotti, Celeste (author)
Novartis Institutes for BioMedical Research, Inc.,Istituto Ortopedico Galeazzi
Papadimitropoulos, Adam (author)
University Hospital Basel
Todorov, Atanas (author)
University Hospital Basel
Epple, Christian (author)
University Hospital Basel
Peretti, Giuseppe M (author)
Istituto Ortopedico Galeazzi,University of Milan
Martin, Ivan (author)
University Hospital Basel
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 (creator_code:org_t)
2020-09-30
2020
English.
In: International Journal of Molecular Sciences. - : MDPI AG. - 1422-0067. ; 21:19
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Most bones of the human body form and heal through endochondral ossification, whereby hypertrophic cartilage (HyC) is formed and subsequently remodeled into bone. We previously demonstrated that HyC can be engineered from human mesenchymal stromal cells (hMSC), and subsequently devitalized by apoptosis induction. The resulting extracellular matrix (ECM) tissue retained osteoinductive properties, leading to ectopic bone formation. In this study, we aimed at engineering and devitalizing upscaled quantities of HyC ECM within a perfusion bioreactor, followed by in vivo assessment in an orthotopic bone repair model. We hypothesized that the devitalized HyC ECM would outperform a clinical product currently used for bone reconstructive surgery. Human MSC were genetically engineered with a gene cassette enabling apoptosis induction upon addition of an adjuvant. Engineered hMSC were seeded, differentiated, and devitalized within a perfusion bioreactor. The resulting HyC ECM was subsequently implanted in a 10-mm rabbit calvarial defect model, with processed human bone (Maxgraft®) as control. Human MSC cultured in the perfusion bioreactor generated a homogenous HyC ECM and were efficiently induced towards apoptosis. Following six weeks of in vivo implantation, microcomputed tomography and histological analyses of the defects revealed an increased bone formation in the defects filled with HyC ECM as compared to Maxgraft®. This work demonstrates the suitability of engineered devitalized HyC ECM as a bone substitute material, with a performance superior to a state-of-the-art commercial graft. Streamlined generation of the devitalized tissue transplant within a perfusion bioreactor is relevant towards standardized and automated manufacturing of a clinical product.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinsk bioteknologi -- Biomaterialvetenskap (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Medical Biotechnology -- Biomaterials Science (hsv//eng)

Keyword

Animals
Apoptosis/genetics
Bone Remodeling/genetics
Bone Substitutes/therapeutic use
Cartilage/growth & development
Cell Differentiation/genetics
Extracellular Matrix/genetics
Humans
Mesenchymal Stem Cell Transplantation
Mesenchymal Stem Cells/cytology
Osteogenesis/genetics
Rabbits
Skull/growth & development
Tissue Engineering/methods
Tissue Scaffolds
Wound Healing/genetics

Publication and Content Type

art (subject category)
ref (subject category)

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