In Vivo Comparison of Hard Tissue Regeneration with Human Mesenchymal Stem Cells Processed with Either the FICOLL Method or the BMAC Method
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
19/10/2012
19/10/2012
2010
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Resumo |
Objective: To compare new bone formation in maxillary sinus augmentation procedures using biomaterial associated with mesenchymal stem cells (MSCs) separated by two different isolation methods. Background: In regenerative medicine open cell concentration systems are only allowed for clinical application under good manufacturing practice conditions. Methods: Mononuclear cells, including MSCs, were concentrated with either the synthetic poylsaccharid (FICOLL) method (classic open system-control group, n = 6 sinus) or the bone marrow aspirate concentrate (BMAC) method (closed system-test group, n = 12 sinus) and transplanted in combination with biomaterial. A sample of the cells was characterized by their ability to differentiate. After 4.1 months (SD +/- 1.0) bone biopsies were obtained and analyzed. Results: The new bone formation in the BMAC group was 19.9% (90% confidence interval [CI], 10.9-29), and in the FICOLL group was 15.5% (90% CI, 8.6-22.4). The 4.4% difference was not significant (90% CI, -4.6-13.5; p = 0.39). MSCs could be differentiated into osteogenic, chondrogenic, and adipogenic lineages. Conclusion: MSCs harvested from bone marrow aspirate in combination with bovine bone matrix particles can form lamellar bone and provide a reliable base for dental implants. The closed BMAC system is suited to substitute the open FICOLL system in bone regeneration procedures. Camlog Foundation, Basel, Switzerland |
Identificador |
TISSUE ENGINEERING PART C-METHODS, v.16, n.2, p.215-223, 2010 1937-3384 http://producao.usp.br/handle/BDPI/26400 10.1089/ten.tec.2009.0269 |
Idioma(s) |
eng |
Publicador |
MARY ANN LIEBERT INC |
Relação |
Tissue Engineering Part C-methods |
Direitos |
restrictedAccess Copyright MARY ANN LIEBERT INC |
Palavras-Chave | #ACUTE MYOCARDIAL-INFARCTION #BONE-MARROW-CELLS #SINUS AUGMENTATION #PROGENITOR CELLS #GRAFTS #MORBIDITY #THERAPY #BLOOD #Cell & Tissue Engineering #Biotechnology & Applied Microbiology #Cell Biology |
Tipo |
article original article publishedVersion |