Journal Article

PreJuSER-19786

http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png Fluorescent lipids: functional parts of fusogenic liposomes and tools for cell membrane labeling and visualization

Kleusch, C.FZJ* ; Hersch, N.FZJ* ; Hoffmann, B.FZJ* ; Merkel, R.FZJ* ; Csiszar, A.FZJ*

2012
MDPI Basel

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Please use a persistent id in citations: http://hdl.handle.net/2128/11532  doi:10.3390/molecules17011055

Abstract: 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.

Keyword(s): Animals (MeSH) ; CHO Cells (MeSH) ; Cell Membrane: chemistry (MeSH) ; Cell Survival: drug effects (MeSH) ; Cricetinae (MeSH) ; Fibroblasts: chemistry (MeSH) ; Fluorescent Dyes: chemistry (MeSH) ; Intracellular Membranes: chemistry (MeSH) ; Liposomes: chemistry (MeSH) ; Membrane Fusion: drug effects (MeSH) ; Membrane Lipids: chemistry (MeSH) ; Membrane Lipids: pharmacology (MeSH) ; Organelles: chemistry (MeSH) ; Rats (MeSH) ; Rats, Wistar (MeSH) ; Staining and Labeling: methods (MeSH) ; Fluorescent Dyes ; Liposomes ; Membrane Lipids ; J ; fusogenic liposomes (auto) ; cellular membrane staining (auto) ; fluorescent lipids (auto) ; DiR (auto) ; Bodipy FL-sphingomyelin (auto) ; fluorescence microscopy (auto)

Note: 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.

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Contributing Institute(s):

1. Biomechanik (ICS-7)

Research Program(s):

1. BioSoft: Makromolekulare Systeme und biologische Informationsverarbeitung (P45)

Appears in the scientific report 2012

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Database coverage:
; ; ; ; Current Contents - Social and Behavioral Sciences ; JCR ; NCBI Molecular Biology Database ; SCOPUS ; Science Citation Index Expanded ; Thomson Reuters Master Journal List ; Web of Science Core Collection

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