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Scanning electron microscopy preparation protocol for differentiated stem cells
Published in
2011
PMID: 21684249
Volume: 416
   
Issue: 2
Pages: 186 - 190
Abstract
The lack of an established protocol for scanning electron microscopy (SEM) studies on stem cells differentiating into adipogenic lineage led us to develop a protocol for the preparation of differentiated adult bone marrow-derived mesenchymal stem cells (BMSC) for SEM. This protocol describes the procedure to maintain and preserve the structural organization of cellular components following differentiation, for morphological and physical characterization. The fixation of the differentiated cells was followed by dehydration using methanol, and vacuum desiccation before microscopy. The use of longer chain alcohols as dehydrating agents was avoided in our method to reduce the dissolution of lipid deposits in cells, thus allowing the maintenance of their structural integrity. The time period for the processing of samples was reduced by avoiding the osmium tetroxide postfixation and critical point drying. Thus, this protocol helps in determining the potential, fate, and degree of stem cell differentiation. This may be useful for SEM analysis of differentiated cells, especially those grown on various scaffolds. © 2011 Elsevier Inc. All rights reserved.
About the journal
JournalAnalytical Biochemistry
ISSN00032697
Open AccessNo
Concepts (32)
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    OSMIUM TETRAOXIDE
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    ADIPOCYTE
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    Animal cell
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    Animal experiment
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    Article
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    BONE MARROW CELL
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    Cell differentiation
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    Cell fate
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    Cell growth
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    Cell structure
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    Controlled study
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    Dehydration
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    Desiccation
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    Dissolution
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    LIPID STORAGE
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    Mesenchymal stem cell
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    Mouse
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    Nonhuman
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    Osteocyte
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    Priority journal
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    Scanning electron microscopy
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    Animal
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    BONE MARROW CELL
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    Chemistry
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    Cytology
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    Methodology
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    Animals
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    Bone marrow cells
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    Mesenchymal stem cells
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    Mice
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    Microscopy, electron, scanning
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    OSMIUM TETROXIDE