Recent advances in live cell imaging of hepatoma cells
Identifieur interne : 000744 ( Pmc/Curation ); précédent : 000743; suivant : 000745Recent advances in live cell imaging of hepatoma cells
Auteurs : Sandeep Salipalli [Allemagne] ; Prafull Kumar Singh [Allemagne] ; Jürgen Borlak [Allemagne]Source :
- BMC Cell Biology [ 1471-2121 ] ; 2014.
Abstract
Live cell imaging enables the study of dynamic processes of living cells in real time by use of suitable reporter proteins and the staining of specific cellular structures and/or organelles. With the availability of advanced optical devices and improved cell culture protocols it has become a rapidly growing research methodology. The success of this technique relies mainly on the selection of suitable reporter proteins, construction of recombinant plasmids possessing cell type specific promoters as well as reliable methods of gene transfer. This review aims to provide an overview of the recent developments in the field of marker proteins (bioluminescence and fluorescent) and methodologies (fluorescent resonance energy transfer, fluorescent recovery after photobleaching and proximity ligation assay) employed as to achieve an improved imaging of biological processes in hepatoma cells. Moreover, different expression systems of marker proteins and the modes of gene transfer are discussed with emphasis on the study of lipid droplet formation in hepatocytes as an example.
Url:
DOI: 10.1186/1471-2121-15-26
PubMed: 25005127
PubMed Central: 4108253
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<front><div type="abstract" xml:lang="en"><p>Live cell imaging enables the study of dynamic processes of living cells in real time by use of suitable reporter proteins and the staining of specific cellular structures and/or organelles. With the availability of advanced optical devices and improved cell culture protocols it has become a rapidly growing research methodology. The success of this technique relies mainly on the selection of suitable reporter proteins, construction of recombinant plasmids possessing cell type specific promoters as well as reliable methods of gene transfer. This review aims to provide an overview of the recent developments in the field of marker proteins (bioluminescence and fluorescent) and methodologies (fluorescent resonance energy transfer, fluorescent recovery after photobleaching and proximity ligation assay) employed as to achieve an improved imaging of biological processes in hepatoma cells. Moreover, different expression systems of marker proteins and the modes of gene transfer are discussed with emphasis on the study of lipid droplet formation in hepatocytes as an example.</p>
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<front><journal-meta><journal-id journal-id-type="nlm-ta">BMC Cell Biol</journal-id>
<journal-id journal-id-type="iso-abbrev">BMC Cell Biol</journal-id>
<journal-title-group><journal-title>BMC Cell Biology</journal-title>
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<issn pub-type="epub">1471-2121</issn>
<publisher><publisher-name>BioMed Central</publisher-name>
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<article-meta><article-id pub-id-type="pmid">25005127</article-id>
<article-id pub-id-type="pmc">4108253</article-id>
<article-id pub-id-type="publisher-id">1471-2121-15-26</article-id>
<article-id pub-id-type="doi">10.1186/1471-2121-15-26</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Review</subject>
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<title-group><article-title>Recent advances in live cell imaging of hepatoma cells</article-title>
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</contrib-group>
<aff id="I1"><label>1</label>
Centre for Pharmacology and Toxicology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625 Hannover, Germany</aff>
<pub-date pub-type="collection"><year>2014</year>
</pub-date>
<pub-date pub-type="epub"><day>8</day>
<month>7</month>
<year>2014</year>
</pub-date>
<volume>15</volume>
<fpage>26</fpage>
<lpage>26</lpage>
<history><date date-type="received"><day>28</day>
<month>11</month>
<year>2013</year>
</date>
<date date-type="accepted"><day>25</day>
<month>6</month>
<year>2014</year>
</date>
</history>
<permissions><copyright-statement>Copyright © 2014 Salipalli et al.; licensee BioMed Central Ltd.</copyright-statement>
<copyright-year>2014</copyright-year>
<copyright-holder>Salipalli et al.; licensee BioMed Central Ltd.</copyright-holder>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/2.0"><license-p>This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/2.0">http://creativecommons.org/licenses/by/2.0</ext-link>
), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/publicdomain/zero/1.0/">http://creativecommons.org/publicdomain/zero/1.0/</ext-link>
) applies to the data made available in this article, unless otherwise stated.</license-p>
</license>
</permissions>
<self-uri xlink:href="http://www.biomedcentral.com/1471-2121/15/26"></self-uri>
<abstract><p>Live cell imaging enables the study of dynamic processes of living cells in real time by use of suitable reporter proteins and the staining of specific cellular structures and/or organelles. With the availability of advanced optical devices and improved cell culture protocols it has become a rapidly growing research methodology. The success of this technique relies mainly on the selection of suitable reporter proteins, construction of recombinant plasmids possessing cell type specific promoters as well as reliable methods of gene transfer. This review aims to provide an overview of the recent developments in the field of marker proteins (bioluminescence and fluorescent) and methodologies (fluorescent resonance energy transfer, fluorescent recovery after photobleaching and proximity ligation assay) employed as to achieve an improved imaging of biological processes in hepatoma cells. Moreover, different expression systems of marker proteins and the modes of gene transfer are discussed with emphasis on the study of lipid droplet formation in hepatocytes as an example.</p>
</abstract>
<kwd-group><kwd>Live cell imaging</kwd>
<kwd>Fluorescence</kwd>
<kwd>Bioluminescence</kwd>
<kwd>Green Fluorescent Protein</kwd>
<kwd>Proximity ligation assay</kwd>
<kwd>Lipid droplet</kwd>
</kwd-group>
</article-meta>
</front>
</pmc>
</record>
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