Morphology and morphometry of feline bone marrow-derived mesenchymal stem cells in culture

Mesenchymal stem cells (MSC) are increasingly being proposed as a therapeutic option for treatment of a variety of different diseases in human and veterinary medicine. Stem cells have been isolated from feline bone marrow, however, very few data exist about the morphology of these cells and no data were found about the morphometry of feline bone marrow-derived MSCs (BM-MSCs). The objectives of this study were the isolation, growth evaluation, differentiation potential and characterization of feline BM-MSCs by their morphological and morphometric characteristics. in vitro differentiation assays were conducted to confirm the multipotency of feline MSC, as assessed by their ability to differentiate into three cell lineages (osteoblasts, chondrocytes, and adipocytes). To evaluate morphological and morphometric characteristics the cells are maintained in culture. Cells were observed with light microscope, with association of dyes, and they were measured at 24, 48, 72 and 120h of culture (P1 and P3). The non-parametric ANOVA test for independent samples was performed and the means were compared by Tukey's test. On average, the number of mononuclear cells obtained was 12.29 (±6.05x10(6)) cells/mL of bone marrow. Morphologically, BM-MSCs were long and fusiforms, and squamous with abundant cytoplasm. In the morphometric study of the cells, it was observed a significant increase in average length of cells during the first passage. The cell lengths were 106.97±38.16µm and 177.91±71.61µm, respectively, at first and third passages (24 h). The cell widths were 30.79±16.75 µm and 40.18±20.46µm, respectively, at first and third passages (24 h).The nucleus length of the feline BM-MSCs at P1 increased from 16.28µm (24h) to 21.29µm (120h). However, at P3, the nucleus length was 26.35µm (24h) and 25.22µm (120h). This information could be important for future application and use of feline BM-MSCs.

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Main Authors: Maciel,Bruno B., Rebelatto,Carmen L.K., Brofman,Paulo R.S., Brito,Harald F.V., Patricio,Lia F.L., Cruz,Marúcia A., Locatelli-Dittrich,Rosangela
Format: Digital revista
Language:English
Published: Colégio Brasileiro de Patologia Animal - CBPA 2014
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-736X2014001100016
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spelling oai:scielo:S0100-736X20140011000162015-01-28Morphology and morphometry of feline bone marrow-derived mesenchymal stem cells in cultureMaciel,Bruno B.Rebelatto,Carmen L.K.Brofman,Paulo R.S.Brito,Harald F.V.Patricio,Lia F.L.Cruz,Marúcia A.Locatelli-Dittrich,Rosangela Feline multipotent stem cell stem cell isolation cell morphometry cell morphology Mesenchymal stem cells (MSC) are increasingly being proposed as a therapeutic option for treatment of a variety of different diseases in human and veterinary medicine. Stem cells have been isolated from feline bone marrow, however, very few data exist about the morphology of these cells and no data were found about the morphometry of feline bone marrow-derived MSCs (BM-MSCs). The objectives of this study were the isolation, growth evaluation, differentiation potential and characterization of feline BM-MSCs by their morphological and morphometric characteristics. in vitro differentiation assays were conducted to confirm the multipotency of feline MSC, as assessed by their ability to differentiate into three cell lineages (osteoblasts, chondrocytes, and adipocytes). To evaluate morphological and morphometric characteristics the cells are maintained in culture. Cells were observed with light microscope, with association of dyes, and they were measured at 24, 48, 72 and 120h of culture (P1 and P3). The non-parametric ANOVA test for independent samples was performed and the means were compared by Tukey's test. On average, the number of mononuclear cells obtained was 12.29 (±6.05x10(6)) cells/mL of bone marrow. Morphologically, BM-MSCs were long and fusiforms, and squamous with abundant cytoplasm. In the morphometric study of the cells, it was observed a significant increase in average length of cells during the first passage. The cell lengths were 106.97±38.16µm and 177.91±71.61µm, respectively, at first and third passages (24 h). The cell widths were 30.79±16.75 µm and 40.18±20.46µm, respectively, at first and third passages (24 h).The nucleus length of the feline BM-MSCs at P1 increased from 16.28µm (24h) to 21.29µm (120h). However, at P3, the nucleus length was 26.35µm (24h) and 25.22µm (120h). This information could be important for future application and use of feline BM-MSCs.info:eu-repo/semantics/openAccessColégio Brasileiro de Patologia Animal - CBPAPesquisa Veterinária Brasileira v.34 n.11 20142014-11-01info:eu-repo/semantics/othertext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-736X2014001100016en10.1590/S0100-736X2014001100016
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language English
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author Maciel,Bruno B.
Rebelatto,Carmen L.K.
Brofman,Paulo R.S.
Brito,Harald F.V.
Patricio,Lia F.L.
Cruz,Marúcia A.
Locatelli-Dittrich,Rosangela
spellingShingle Maciel,Bruno B.
Rebelatto,Carmen L.K.
Brofman,Paulo R.S.
Brito,Harald F.V.
Patricio,Lia F.L.
Cruz,Marúcia A.
Locatelli-Dittrich,Rosangela
Morphology and morphometry of feline bone marrow-derived mesenchymal stem cells in culture
author_facet Maciel,Bruno B.
Rebelatto,Carmen L.K.
Brofman,Paulo R.S.
Brito,Harald F.V.
Patricio,Lia F.L.
Cruz,Marúcia A.
Locatelli-Dittrich,Rosangela
author_sort Maciel,Bruno B.
title Morphology and morphometry of feline bone marrow-derived mesenchymal stem cells in culture
title_short Morphology and morphometry of feline bone marrow-derived mesenchymal stem cells in culture
title_full Morphology and morphometry of feline bone marrow-derived mesenchymal stem cells in culture
title_fullStr Morphology and morphometry of feline bone marrow-derived mesenchymal stem cells in culture
title_full_unstemmed Morphology and morphometry of feline bone marrow-derived mesenchymal stem cells in culture
title_sort morphology and morphometry of feline bone marrow-derived mesenchymal stem cells in culture
description Mesenchymal stem cells (MSC) are increasingly being proposed as a therapeutic option for treatment of a variety of different diseases in human and veterinary medicine. Stem cells have been isolated from feline bone marrow, however, very few data exist about the morphology of these cells and no data were found about the morphometry of feline bone marrow-derived MSCs (BM-MSCs). The objectives of this study were the isolation, growth evaluation, differentiation potential and characterization of feline BM-MSCs by their morphological and morphometric characteristics. in vitro differentiation assays were conducted to confirm the multipotency of feline MSC, as assessed by their ability to differentiate into three cell lineages (osteoblasts, chondrocytes, and adipocytes). To evaluate morphological and morphometric characteristics the cells are maintained in culture. Cells were observed with light microscope, with association of dyes, and they were measured at 24, 48, 72 and 120h of culture (P1 and P3). The non-parametric ANOVA test for independent samples was performed and the means were compared by Tukey's test. On average, the number of mononuclear cells obtained was 12.29 (±6.05x10(6)) cells/mL of bone marrow. Morphologically, BM-MSCs were long and fusiforms, and squamous with abundant cytoplasm. In the morphometric study of the cells, it was observed a significant increase in average length of cells during the first passage. The cell lengths were 106.97±38.16µm and 177.91±71.61µm, respectively, at first and third passages (24 h). The cell widths were 30.79±16.75 µm and 40.18±20.46µm, respectively, at first and third passages (24 h).The nucleus length of the feline BM-MSCs at P1 increased from 16.28µm (24h) to 21.29µm (120h). However, at P3, the nucleus length was 26.35µm (24h) and 25.22µm (120h). This information could be important for future application and use of feline BM-MSCs.
publisher Colégio Brasileiro de Patologia Animal - CBPA
publishDate 2014
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-736X2014001100016
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