The use of mesenchymal stromal cell secretome to enhance guided bone regeneration in comparison with leukocyte and platelet‐rich fibrin

Author:

Shanbhag Siddharth12ORCID,Al‐Sharabi Niyaz2ORCID,Kampleitner Carina345,Mohamed‐Ahmed Samih2,Kristoffersen Einar K.1,Tangl Stefan35,Mustafa Kamal2,Gruber Reinhard567ORCID,Sanz Mariano8

Affiliation:

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

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

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

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

5. Austrian Cluster for Tissue Regeneration Vienna Austria

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

7. Department of Periodontology School of Dental Medicine, University of Bern Bern Switzerland

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

Abstract

AbstractObjectivesSecretomes of mesenchymal stromal cells (MSC) represent a novel strategy for growth‐factor delivery for tissue regeneration. The objective of this study was to compare the efficacy of adjunctive use of conditioned media of bone‐marrow MSC (MSC‐CM) with collagen barrier membranes vs. adjunctive use of conditioned media of leukocyte‐ and platelet‐rich fibrin (PRF‐CM), a current growth‐factor therapy, for guided bone regeneration (GBR).MethodsMSC‐CM and PRF‐CM prepared from healthy human donors were subjected to proteomic analysis using mass spectrometry and multiplex immunoassay. Collagen membranes functionalized with MSC‐CM or PRF‐CM were applied on critical‐size rat calvaria defects and new bone formation was assessed via three‐dimensional (3D) micro‐CT analysis of total defect volume (2 and 4 weeks) and 2D histomorphometric analysis of central defect regions (4 weeks).ResultsWhile both MSC‐CM and PRF‐CM revealed several bone‐related proteins, differentially expressed proteins, especially extracellular matrix components, were increased in MSC‐CM. In rat calvaria defects, micro‐CT revealed greater total bone coverage in the MSC‐CM group after 2 and 4 weeks. Histologically, both groups showed a combination of regular new bone and ‘hybrid’ new bone, which was formed within the membrane compartment and characterized by incorporation of mineralized collagen fibers. Histomorphometry in central defect sections revealed greater hybrid bone area in the MSC‐CM group, while the total new bone area was similar between groups.ConclusionBased on the in vitro and in vivo investigations herein, functionalization of membranes with MSC‐CM represents a promising strategy to enhance GBR.

Funder

Osteology Foundation

Publisher

Wiley

Subject

Oral Surgery

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