TY - JOUR
T1 - Mesenchymal stem cells and three-dimensional-osteoconductive scaffold regenerate calvarial bone in critical size defects in swine
AU - Johnson, Zoe M.
AU - Yuan, Yuan
AU - Li, Xiangjia
AU - Jashashvili, Tea
AU - Jamieson, Michael
AU - Urata, Mark
AU - Chen, Yong
AU - Chai, Yang
N1 - Funding Information:
We thank Bridget Samuels for critical reading of the manuscript. This work was supported by the National Institute of Dental and Craniofacial Research National Institute of Health—Center for Dental, Oral and Craniofacial Tissue and Organ Regeneration (C‐DOCTOR) U24 DE026914; U24 DE029463 and Alfred Mann Institute (AMI) at the University of Southern California.
Funding Information:
We thank Bridget Samuels for critical reading of the manuscript. This work was supported by the National Institute of Dental and Craniofacial Research National Institute of Health?Center for Dental, Oral and Craniofacial Tissue and Organ Regeneration (C-DOCTOR) U24 DE026914; U24 DE029463 and Alfred Mann Institute (AMI) at the University of Southern California.
Publisher Copyright:
© 2021 The Authors. STEM CELLS TRANSLATIONAL MEDICINE published by Wiley Periodicals LLC on behalf of AlphaMed Press.
PY - 2021/8
Y1 - 2021/8
N2 - 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.
AB - 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.
KW - bone marrow aspirate
KW - critical size defect
KW - dental pulp neural crest cell
KW - hydroxyapatite tricalcium phosphate
KW - mesenchymal stem cells
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U2 - 10.1002/sctm.20-0534
DO - 10.1002/sctm.20-0534
M3 - Article
C2 - 33794062
AN - SCOPUS:85103850405
SN - 2157-6564
VL - 10
SP - 1170
EP - 1183
JO - Stem cells translational medicine
JF - Stem cells translational medicine
IS - 8
ER -