Osteoprogenitor cells can enhance early bone formation in critical bone defects in dogs

ABSTRACT: The aim of this study was to evaluate the effect of osteoprogenitor cells derived from mesenchymal stem cells from adipose tissue (OC-AD-MSCs), and differentiated into osteoblasts, in the treatment of critical bone defects in dogs. Adipose tissue derived mesenchymal stem cells (AD-MSCs) were subjected to osteogenic differentiation for 21 days and used in the treatment of bone defects in dogs radius. Either three experimental groups were bone defects treated with OC-AD-MSCs (OC), defects filled with autogenous bone (Control- C +), or empty defects (Control- C -). Bone regeneration was assessed by radiology, densitometry, and histomorphometry. The area of new bone formation was higher in the OC group compared to the control group (C-) on postoperative day 15. Defects treated with OC-AD-MSCs showed greater neovascularization than the other two groups at 90 days. We concluded that treatment with OC-AD-MSCs increased the area of new bone formation 15 days after surgery; however, it didn’t complete the bone union in critical bone defects in the radius of dogs at 90 days.

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Main Authors: Alves,Endrigo Gabellini Leonel, Serakides,Rogéria, Rosado,Isabel Rodrigues, Paez,Omar Leonardo Aristizabal, Varon,Jéssica Alejandra Castro, Machado,Felipe Nemer, Fukushima,Fabíola Bono, Góes,Alfredo Miranda, Rezende,Cleuza Maria de Faria
Format: Digital revista
Language:English
Published: Universidade Federal de Santa Maria 2017
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-84782017000700604
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spelling oai:scielo:S0103-847820170007006042017-11-22Osteoprogenitor cells can enhance early bone formation in critical bone defects in dogsAlves,Endrigo Gabellini LeonelSerakides,RogériaRosado,Isabel RodriguesPaez,Omar Leonardo AristizabalVaron,Jéssica Alejandra CastroMachado,Felipe NemerFukushima,Fabíola BonoGóes,Alfredo MirandaRezende,Cleuza Maria de Faria bone regeneration orthopedics cellular therapy fracture non-union ABSTRACT: The aim of this study was to evaluate the effect of osteoprogenitor cells derived from mesenchymal stem cells from adipose tissue (OC-AD-MSCs), and differentiated into osteoblasts, in the treatment of critical bone defects in dogs. Adipose tissue derived mesenchymal stem cells (AD-MSCs) were subjected to osteogenic differentiation for 21 days and used in the treatment of bone defects in dogs radius. Either three experimental groups were bone defects treated with OC-AD-MSCs (OC), defects filled with autogenous bone (Control- C +), or empty defects (Control- C -). Bone regeneration was assessed by radiology, densitometry, and histomorphometry. The area of new bone formation was higher in the OC group compared to the control group (C-) on postoperative day 15. Defects treated with OC-AD-MSCs showed greater neovascularization than the other two groups at 90 days. We concluded that treatment with OC-AD-MSCs increased the area of new bone formation 15 days after surgery; however, it didn’t complete the bone union in critical bone defects in the radius of dogs at 90 days.info:eu-repo/semantics/openAccessUniversidade Federal de Santa MariaCiência Rural v.47 n.7 20172017-01-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-84782017000700604en10.1590/0103-8478cr20151109
institution SCIELO
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country Brasil
countrycode BR
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databasecode rev-scielo-br
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region America del Sur
libraryname SciELO
language English
format Digital
author Alves,Endrigo Gabellini Leonel
Serakides,Rogéria
Rosado,Isabel Rodrigues
Paez,Omar Leonardo Aristizabal
Varon,Jéssica Alejandra Castro
Machado,Felipe Nemer
Fukushima,Fabíola Bono
Góes,Alfredo Miranda
Rezende,Cleuza Maria de Faria
spellingShingle Alves,Endrigo Gabellini Leonel
Serakides,Rogéria
Rosado,Isabel Rodrigues
Paez,Omar Leonardo Aristizabal
Varon,Jéssica Alejandra Castro
Machado,Felipe Nemer
Fukushima,Fabíola Bono
Góes,Alfredo Miranda
Rezende,Cleuza Maria de Faria
Osteoprogenitor cells can enhance early bone formation in critical bone defects in dogs
author_facet Alves,Endrigo Gabellini Leonel
Serakides,Rogéria
Rosado,Isabel Rodrigues
Paez,Omar Leonardo Aristizabal
Varon,Jéssica Alejandra Castro
Machado,Felipe Nemer
Fukushima,Fabíola Bono
Góes,Alfredo Miranda
Rezende,Cleuza Maria de Faria
author_sort Alves,Endrigo Gabellini Leonel
title Osteoprogenitor cells can enhance early bone formation in critical bone defects in dogs
title_short Osteoprogenitor cells can enhance early bone formation in critical bone defects in dogs
title_full Osteoprogenitor cells can enhance early bone formation in critical bone defects in dogs
title_fullStr Osteoprogenitor cells can enhance early bone formation in critical bone defects in dogs
title_full_unstemmed Osteoprogenitor cells can enhance early bone formation in critical bone defects in dogs
title_sort osteoprogenitor cells can enhance early bone formation in critical bone defects in dogs
description ABSTRACT: The aim of this study was to evaluate the effect of osteoprogenitor cells derived from mesenchymal stem cells from adipose tissue (OC-AD-MSCs), and differentiated into osteoblasts, in the treatment of critical bone defects in dogs. Adipose tissue derived mesenchymal stem cells (AD-MSCs) were subjected to osteogenic differentiation for 21 days and used in the treatment of bone defects in dogs radius. Either three experimental groups were bone defects treated with OC-AD-MSCs (OC), defects filled with autogenous bone (Control- C +), or empty defects (Control- C -). Bone regeneration was assessed by radiology, densitometry, and histomorphometry. The area of new bone formation was higher in the OC group compared to the control group (C-) on postoperative day 15. Defects treated with OC-AD-MSCs showed greater neovascularization than the other two groups at 90 days. We concluded that treatment with OC-AD-MSCs increased the area of new bone formation 15 days after surgery; however, it didn’t complete the bone union in critical bone defects in the radius of dogs at 90 days.
publisher Universidade Federal de Santa Maria
publishDate 2017
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-84782017000700604
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