Bone Regeneration Induced by Bone Porcine Block with Bone Marrow Stromal Stem Cells in a Minipig Model of Mandibular “Critical Size” Defect

Author:

Scarano Antonio1ORCID,Crincoli Vito2ORCID,Di Benedetto Adriana3,Cozzolino Valerio1,Lorusso Felice1ORCID,Podaliri Vulpiani Michele4,Grano Maria5,Kalemaj Zamira6,Mori Giorgio3ORCID,Grassi Felice Roberto7

Affiliation:

1. Department of Medical, Oral and Biotechnological Sciences and CeSI-Met, University of Chieti-Pescara, Chieti, Italy

2. Interdisciplinary Department of Medicine, University of Bari "A. Moro", Bari, Italy

3. Department of Clinical and Experimental Medicine, Medical School, University of Foggia, Foggia, Italy

4. Department of Animals Sperimentation, Istituto Zooprofilattico Sperimentale dell'Abruzzo e del Molise "G. Caporale", Teramo, Italy

5. Department of Emergency and Organ Transplantation, University of Bari "A. Moro", Bari, Italy

6. Department of Surgical Sciences, Dental School, University of Turin, Torino, Italy

7. Department of Basic and Medical Sciences, Neurosciences and Sense Organs, University of Bari, Bari, Italy

Abstract

Introduction. Adding stem cells to biodegradable scaffolds to enhance bone regeneration is a valuable option. Different kinds of stem cells with osteoblastic activity were tested, such as bone marrow stromal stem cells (BMSSCs). Aim. To assess a correct protocol for osteogenic stem cell differentiation, so BMSSCs were seeded on a bone porcine block (BPB). Materials and Methods. Bone marrow from six minipigs was extracted from tibiae and humeri and treated to isolate BMSSCs. After seeding on BPB, critical-size defects were created on each mandible of the minipigs and implanted with BPB and BPB/BMSSCs. After three months, histomorphometric analysis was performed. Results. Histomorphometric analysis provided percentages of the three groups. Tissues present in control defects were 23 ± 2% lamellar bone, 28 ± 1% woven bone, and 56 ± 4% marrow spaces; in BPB defects were 20 ± 5% BPB, 32 ± 2% lamellar bone, 24 ± 1% woven bone, and 28 ± 2% marrow spaces; in BPB/BMSSCs defects were 17 ± 4% BPB/BMSSCs, 42 ± 2% lamellar bone, 12 ± 1% woven bone, and 22 ± 3% marrow spaces. Conclusion. BPB used as a scaffold to induce bone regeneration may benefit from the addition of BDPSCs in the tissue-engineered constructs.

Funder

Ministry of Education, University, Research

Publisher

Hindawi Limited

Subject

Cell Biology,Molecular Biology

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