Functionalizing Collagen Membranes with MSC-Conditioned Media Promotes Guided Bone Regeneration in Rat Calvarial Defects

Author:

Shanbhag Siddharth12,Kampleitner Carina345ORCID,Al-Sharabi Niyaz2ORCID,Mohamed-Ahmed Samih2ORCID,Apaza Alccayhuaman Karol Ali6ORCID,Heimel Patrick345ORCID,Tangl Stefan35ORCID,Beinlich Andreas7ORCID,Rana Neha2ORCID,Sanz Mariano8,Kristoffersen Einar K.1ORCID,Mustafa Kamal2ORCID,Gruber Reinhard569

Affiliation:

1. Department of Immunology and Transfusion Medicine, Haukeland University Hospital, 5021 Bergen, Norway

2. Center for Translational Oral Research (TOR), Department of Clinical Dentistry, Faculty of Medicine, University of Bergen, 5009 Bergen, Norway

3. Karl Donath Laboratory for Hard Tissue and Biomaterial Research, University Clinic of Dentistry, Medical University of Vienna, 1090 Vienna, Austria

4. Ludwig Boltzmann Institute for Traumatology, The Research Center in Cooperation with AUVA, 1200 Vienna, Austria

5. Austrian Cluster for Tissue Regeneration, 1200 Vienna, Austria

6. Department of Oral Biology, University Clinic of Dentistry, Medical University of Vienna, 1090 Vienna, Austria

7. Department of Earth Science, Faculty of Mathematics and Natural Sciences, University of Bergen, 5009 Bergen, Norway

8. ETEP Research Group, Faculty of Odontology, University Complutense of Madrid, 28040 Madrid, Spain

9. Department of Periodontology, School of Dental Medicine, University of Bern, 3010 Bern, Switzerland

Abstract

Functionalizing biomaterials with conditioned media (CM) from mesenchymal stromal cells (MSC) is a promising strategy for enhancing the outcomes of guided bone regeneration (GBR). This study aimed to evaluate the bone regenerative potential of collagen membranes (MEM) functionalized with CM from human bone marrow MSC (MEM-CM) in critical size rat calvarial defects. MEM-CM prepared via soaking (CM-SOAK) or soaking followed by lyophilization (CM-LYO) were applied to critical size rat calvarial defects. Control treatments included native MEM, MEM with rat MSC (CEL) and no treatment. New bone formation was analyzed via micro-CT (2 and 4 weeks) and histology (4 weeks). Greater radiographic new bone formation occurred at 2 weeks in the CM-LYO group vs. all other groups. After 4 weeks, only the CM-LYO group was superior to the untreated control group, whereas the CM-SOAK, CEL and native MEM groups were similar. Histologically, the regenerated tissues showed a combination of regular new bone and hybrid new bone, which formed within the membrane compartment and was characterized by the incorporation of mineralized MEM fibers. Areas of new bone formation and MEM mineralization were greatest in the CM-LYO group. Proteomic analysis of lyophilized CM revealed the enrichment of several proteins and biological processes related to bone formation. In summary, lyophilized MEM-CM enhanced new bone formation in rat calvarial defects, thus representing a novel ‘off-the-shelf’ strategy for GBR.

Funder

Osteology Foundation, Switzerland

Research Council of Norway

Helse Vest Research Funding, Norway

Olav Thon Foundation, Norway

Trond Mohn Foundation

Publisher

MDPI AG

Subject

General Medicine

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