Membrane domain formation, interdigitation, and morphological alterations induced by the very long chain asymmetric C24:1 ceramide

被引:92
作者
Pinto, Sandra N. [1 ]
Silva, Liana C. [1 ]
de Almeida, Rodrigo F. M. [2 ]
Prieto, Manuel [1 ]
机构
[1] Inst Super Tecn, Ctr Quim Fis Mol, P-1049001 Lisbon, Portugal
[2] Univ Lisbon, Fac Ciencias, Ctr Quim & Bioquim, P-1749016 Lisbon, Portugal
关键词
D O I
10.1529/biophysj.108.129858
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Ceramide (Cer) is involved in the regulation of several biological processes, such as apoptosis and cell signaling. The alterations induced by Cer in the biophysical properties of membranes are thought to be one of the major routes of Cer action. To gain further knowledge about the alterations induced by Cer, membrane reorganization by the very long chain asymmetric nervonoylceramide (NCer) was studied. The application of an established fluorescence multiprobe approach, together with x-ray diffraction, differential scanning calorimetry, and confocal fluorescence microscopy, allowed the characterization of NCer and the determination of the phase diagram of palmitoyloleoylphosphatidylcholine (POPC)/NCer binary mixtures. Nervonoylceramide undergoes a transition from a mixed interdigitated gel phase to a partially interdigitated gel phase at similar to 20 degrees C, and a broad main transition to the fluid phase at similar to 52 degrees C. The solubility of NCer in the fluid POPC is low, driving gel fluid phase separation, and the binary-phase diagram is characterized by multiple and large coexistence regions between the interdigitated gel phases and the fluid phase. At 37 degrees C, the relevant phases are the fluid and the partially interdigitated gel. Moreover, the formation of NCer interdigitated gel phases leads to strong morphological alterations in the lipid vesicles, driving the formation of cochleate-type tubular structures.
引用
收藏
页码:2867 / 2879
页数:13
相关论文
共 65 条
[1]   Lipid peroxides promote large rafts: Effects of excitation of probes in fluorescence microscopy and electrochemical reactions during vesicle formation [J].
Ayuyan, Artem G. ;
Cohen, Fredric S. .
BIOPHYSICAL JOURNAL, 2006, 91 (06) :2172-2183
[2]   LIPID INTERMOLECULAR HYDROGEN-BONDING - INFLUENCE ON STRUCTURAL ORGANIZATION AND MEMBRANE-FUNCTION [J].
BOGGS, JM .
BIOCHIMICA ET BIOPHYSICA ACTA, 1987, 906 (03) :353-404
[3]  
Carrer DC, 1999, J LIPID RES, V40, P1978
[4]   Effects of a short-chain ceramide on bilayer domain formation, thickness, and chain mobililty: DMPC and asymmetric ceramide mixtures [J].
Carrer, DC ;
Schreier, S ;
Patrito, M ;
Maggio, B .
BIOPHYSICAL JOURNAL, 2006, 90 (07) :2394-2403
[5]   Ceramide modulates the lipid membrane organization at molecular and supramolecular levels [J].
Carrer, DC ;
Härtel, S ;
Mónaco, HL ;
Maggio, B .
CHEMISTRY AND PHYSICS OF LIPIDS, 2003, 122 (1-2) :147-152
[6]   Formation of Ceramide/Sphingomyelin gel domains in the presence of an unsaturated phospholipid: A quantitative multiprobe approach [J].
Castro, Bruno M. ;
de Almeida, Rodrigo F. M. ;
Silva, Liana C. ;
Fedorov, Alexander ;
Prieto, Manuel .
BIOPHYSICAL JOURNAL, 2007, 93 (05) :1639-1650
[7]   Fourier transform infrared spectroscopy and differential scanning calorimetry studies of fatty acid homogeneous ceramide 2 [J].
Chen, HC ;
Mendelsohn, R ;
Rerek, ME ;
Moore, DJ .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2000, 1468 (1-2) :293-303
[8]   Asymmetric addition of ceramides but not dihydroceramides promotes transbilayer (flip-flop) lipid motion in membranes [J].
Contreras, FX ;
Basañez, G ;
Alonso, A ;
Herrmann, A ;
Goñi, FM .
BIOPHYSICAL JOURNAL, 2005, 88 (01) :348-359
[9]   Sphingomyelinase activity causes transbilayer lipid translocation in model and cell membranes [J].
Contreras, FX ;
Villar, AV ;
Alonso, A ;
Kolesnick, RN ;
Goñi, FM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (39) :37169-37174
[10]   Lipid rafts have different sizes depending on membrane composition: A time-resolved fluorescence resonance energy transfer study [J].
de Almeida, RFM ;
Loura, LMS ;
Fedorov, A ;
Prieto, M .
JOURNAL OF MOLECULAR BIOLOGY, 2005, 346 (04) :1109-1120