TY - JOUR
T1 - Prediction of neural differentiation fate of rat mesenchymal stem cells by quantitative morphological analyses using image processing techniques
AU - Kazemimoghadam, Mahdieh
AU - Janmaleki, Mohsen
AU - Fouani, Mohamad Hassan
AU - Abbasi, Sara
N1 - Funding Information:
Acknowledgments: The authors would like to thank Dr. H. Peirovi, head of the Medical Nanotechnology and Tissue Engineering Research Center for his invaluable advices and Y. Fouani at Department of Molecular Genetics, Faculty of Biological Sciences, Tarbiat Modares University for his help in setting up and analyzing RT-PCR experiments. This work was financially supported by the Medical Nanotechnology and Tissue Engineering Research Center, Shahid Beheshti University of Medical Sciences. The paper is based on master thesis titled “Viability and Morphological Analysis of Rat Bone Marrow Mesenchymal Stem Cells during Differentiation into Neural Cells In Vitro and in the Presence of Magnetic Field”.
Publisher Copyright:
© 2015, Walter de Gruyter GmbH. All rights reserved.
PY - 2015/2/1
Y1 - 2015/2/1
N2 - Differentiation of bone marrow mesenchymal stem cells (BMSCs) into neural cells has received significant attention in recent years. However, there is still no practical method to evaluate differentiation process non-invasively and practically. The cellular quality evaluation method is still limited to conventional techniques, which are based on extracting genes or proteins from the cells. These techniques are invasive, costly, time consuming, and should be performed by relevant experts in equipped laboratories. Moreover, they cannot anticipate the future status of cells. Recently, cell morphology has been introduced as a feasible way of monitoring cell behavior because of its relationship with cell proliferation, functions and differentiation. In this study, rat BMSCs were induced to differentiate into neurons. Subsequently, phase contrast images of cells taken at certain intervals were subjected to a series of image processing steps and cell morphology features were calculated. In order to validate the viability of applying image-based approaches for estimating the quality of differentiation process, neural-specific markers were measured experimentally throughout the induction. The strong correlation between quantitative imaging metrics and experimental outcomes revealed the capability of the proposed approach as an auxiliary method of assessing cell behavior during differentiation.
AB - Differentiation of bone marrow mesenchymal stem cells (BMSCs) into neural cells has received significant attention in recent years. However, there is still no practical method to evaluate differentiation process non-invasively and practically. The cellular quality evaluation method is still limited to conventional techniques, which are based on extracting genes or proteins from the cells. These techniques are invasive, costly, time consuming, and should be performed by relevant experts in equipped laboratories. Moreover, they cannot anticipate the future status of cells. Recently, cell morphology has been introduced as a feasible way of monitoring cell behavior because of its relationship with cell proliferation, functions and differentiation. In this study, rat BMSCs were induced to differentiate into neurons. Subsequently, phase contrast images of cells taken at certain intervals were subjected to a series of image processing steps and cell morphology features were calculated. In order to validate the viability of applying image-based approaches for estimating the quality of differentiation process, neural-specific markers were measured experimentally throughout the induction. The strong correlation between quantitative imaging metrics and experimental outcomes revealed the capability of the proposed approach as an auxiliary method of assessing cell behavior during differentiation.
KW - Cell behavior
KW - Correlation
KW - Gene expression
KW - Morphological characteristics
KW - Stem cells
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U2 - 10.1515/bmt-2014-0042
DO - 10.1515/bmt-2014-0042
M3 - Article
C2 - 25324434
AN - SCOPUS:84925355097
SN - 0013-5585
VL - 60
SP - 57
EP - 64
JO - Biomedizinische Technik
JF - Biomedizinische Technik
IS - 1
ER -