Mesenchymal Stem Cells and Three-Dimensional-Osteoconductive Scaffold Regenerate Calvarial Bone in Critical Size Defects in Swine

Author:

Johnson Zoe M.1ORCID,Yuan Yuan1,Li Xiangjia23,Jashashvili Tea4,Jamieson Michael5,Urata Mark6,Chen Yong3,Chai Yang1ORCID

Affiliation:

1. Center for Craniofacial Molecular Biology, Herman Ostrow School of Dentistry  University of Southern California, Los Angeles, California, USA

2. Department of Aerospace and Mechanical Engineering  School for Engineering of Matter, Transport and Energy, Arizona State University, Tempe, Arizona, USA

3. Viterbi School of Engineering, University of Southern California, Los Angeles, California, USA

4. Molecular Imaging Core, University of Southern California, Los Angeles, California, USA

5. Ottawa Hospital Research Institute, Ottawa, Canada

6. Division of Plastic and Maxillofacial Surgery  Children's Hospital Los Angeles, Los Angeles, California, USA

Abstract

Abstract Craniofacial bones protect vital organs, perform important physiological functions, and shape facial identity. Critical-size defects (CSDs) in calvarial bones, which will not heal spontaneously, are caused by trauma, congenital defects, or tumor resections. They pose a great challenge for patients and physicians, and significantly compromise quality of life. Currently, calvarial CSDs are treated either by allogenic or autologous grafts, metal or other synthetic plates that are associated with considerable complications. While previous studies have explored tissue regeneration for calvarial defects, most have been done in small animal models with limited translational value. Here we define a swine calvarial CSD model and show a novel approach to regenerate high-quality bone in these defects by combining mesenchymal stem cells (MSCs) with a three-dimensional (3D)-printed osteoconductive HA/TCP scaffold. Specifically, we have compared the performance of dental pulp neural crest MSCs (DPNCCs) to bone marrow aspirate (BMA) combined with a 3D-printed HA/TCP scaffold to regenerate bone in a calvarial CSD (>7.0 cm2). Both DPNCCs and BMA loaded onto the 3D-printed osteoconductive scaffold support the regeneration of calvarial bone with density, compression strength, and trabecular structures similar to native bone. Our study demonstrates a novel application of an original scaffold design combined with DPNCCs or BMA to support regeneration of high-quality bone in a newly defined and clinically relevant swine calvarial CSD model. This discovery may have important impact on bone regeneration beyond the craniofacial region and will ultimately benefit patients who suffer from debilitating CSDs.

Funder

Alfred Mann Institute (AMI) at the University of Southern California

National Institute of Dental and Craniofacial Research National Institute of Health—Center for Dental, Oral and Craniofacial Tissue and Organ Regeneration

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,General Medicine

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