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024 7 _ |a pmid:22267193
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024 7 _ |a 10.3390/molecules17011055
|2 DOI
024 7 _ |a WOS:000299535700072
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024 7 _ |a 1420-3049
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024 7 _ |a 2128/11532
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037 _ _ |a PreJuSER-19786
041 _ _ |a eng
082 _ _ |a 540
084 _ _ |2 WoS
|a Chemistry, Organic
100 1 _ |a Kleusch, C.
|b 0
|u FZJ
|0 P:(DE-Juel1)VDB104414
245 _ _ |a Fluorescent lipids: functional parts of fusogenic liposomes and tools for cell membrane labeling and visualization
260 _ _ |c 2012
|a Basel
|b MDPI
300 _ _ |a 1055 - 1073
336 7 _ |a Journal Article
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336 7 _ |a JOURNAL_ARTICLE
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336 7 _ |a article
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440 _ 0 |a Molecules
|0 24782
|y 1
|v 17
500 _ _ |a We thank Gerhild van Echten-Deckert for helpful discussions and Simon Ludwanowski, who produced many of the fusogenic liposomes used in this study. Our work was fully funded by the Helmholtz Association.
520 _ _ |a In this paper a rapid and highly efficient method for controlled incorporation of fluorescent lipids into living mammalian cells is introduced. Here, the fluorescent molecules have two consecutive functions: First, they trigger rapid membrane fusion between cellular plasma membranes and the lipid bilayers of their carrier particles, so called fusogenic liposomes, and second, after insertion into cellular membranes these molecules enable fluorescence imaging of cell membranes and membrane traffic processes. We tested the fluorescent derivatives of the following essential membrane lipids for membrane fusion: Ceramide, sphingomyelin, phosphocholine, phosphatidylinositol-bisphosphate, ganglioside, cholesterol, and cholesteryl ester. Our results show that all probed lipids could more efficiently be incorporated into the plasma membrane of living cells than by using other methods. Moreover, labeling occurred in a gentle manner under classical cell culture conditions reducing cellular stress responses. Staining procedures were monitored by fluorescence microscopy and it was observed that sphingolipids and cholesterol containing free hydroxyl groups exhibit a decreased distribution velocity as well as a longer persistence in the plasma membrane compared to lipids without hydroxyl groups like phospholipids or other artificial lipid analogs. After membrane staining, the fluorescent molecules were sorted into membranes of cell organelles according to their chemical properties and biological functions without any influence of the delivery system.
536 _ _ |a BioSoft: Makromolekulare Systeme und biologische Informationsverarbeitung
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588 _ _ |a Dataset connected to Web of Science, Pubmed
650 _ 2 |2 MeSH
|a Animals
650 _ 2 |2 MeSH
|a CHO Cells
650 _ 2 |2 MeSH
|a Cell Membrane: chemistry
650 _ 2 |2 MeSH
|a Cell Survival: drug effects
650 _ 2 |2 MeSH
|a Cricetinae
650 _ 2 |2 MeSH
|a Fibroblasts: chemistry
650 _ 2 |2 MeSH
|a Fluorescent Dyes: chemistry
650 _ 2 |2 MeSH
|a Intracellular Membranes: chemistry
650 _ 2 |2 MeSH
|a Liposomes: chemistry
650 _ 2 |2 MeSH
|a Membrane Fusion: drug effects
650 _ 2 |2 MeSH
|a Membrane Lipids: chemistry
650 _ 2 |2 MeSH
|a Membrane Lipids: pharmacology
650 _ 2 |2 MeSH
|a Organelles: chemistry
650 _ 2 |2 MeSH
|a Rats
650 _ 2 |2 MeSH
|a Rats, Wistar
650 _ 2 |2 MeSH
|a Staining and Labeling: methods
650 _ 7 |0 0
|2 NLM Chemicals
|a Fluorescent Dyes
650 _ 7 |0 0
|2 NLM Chemicals
|a Liposomes
650 _ 7 |0 0
|2 NLM Chemicals
|a Membrane Lipids
650 _ 7 |a J
|2 WoSType
653 2 0 |2 Author
|a fusogenic liposomes
653 2 0 |2 Author
|a cellular membrane staining
653 2 0 |2 Author
|a fluorescent lipids
653 2 0 |2 Author
|a DiR
653 2 0 |2 Author
|a Bodipy FL-sphingomyelin
653 2 0 |2 Author
|a fluorescence microscopy
700 1 _ |a Hersch, N.
|b 1
|u FZJ
|0 P:(DE-Juel1)VDB29396
700 1 _ |a Hoffmann, B.
|b 2
|u FZJ
|0 P:(DE-Juel1)VDB27696
700 1 _ |a Merkel, R.
|b 3
|u FZJ
|0 P:(DE-Juel1)128833
700 1 _ |a Csiszar, A.
|b 4
|u FZJ
|0 P:(DE-Juel1)128805
773 _ _ |0 PERI:(DE-600)2008644-1
|a 10.3390/molecules17011055
|g Vol. 17, p. 1055 - 1073
|p 1055 - 1073
|q 17<1055 - 1073
|t Molecules
|v 17
|x 1420-3049
|y 2012
856 7 _ |u http://dx.doi.org/10.3390/molecules17011055
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914 1 _ |y 2012
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