TY - JOUR
T1 - Effect of glucosylceramide on the biophysical properties of fluid membranes
AU - Varela, Ana R.P.
AU - Gonçalves Da Silva, Amélia M.P.S.
AU - Fedorov, Alexander
AU - Futerman, Anthony H.
AU - Prieto, Manuel
AU - Silva, Liana C.
N1 - Fundacao para a Ciencia e Tecnologia (FCT), Portugal [PTDC/QUI-BIQ/111411/2009]; FCT [SFRH/BD/69982/2010]; FCTThis work was supported by PTDC/QUI-BIQ/111411/2009 from Fundacao para a Ciencia e Tecnologia (FCT), Portugal. FCT provided a research grant to A.R.P. Varela (SFRH/BD/69982/2010). L.C. Silva acknowledges funding from Compromisso para a Ciencia 2008 from FCT. A. Fedorov acknowledges funding from Compromisso para a Ciencia 2007 from FCT. A. H. Futerman is The Joseph Meyerhoff Professor of Biochemistry at the Weizmann Institute of Science.
PY - 2013/3
Y1 - 2013/3
N2 - Glucosylceramide (GlcCer), a relevant intermediate in the pathways of glycosphingolipid metabolism, plays key roles in the regulation of cell physiology. The molecular mechanisms by which GlcCer regulates cellular processes are unknown, but might involve changes in membrane biophysical properties and formation of lipid domains. In the present study, fluorescence spectroscopy, confocal microscopy and surface pressure-area (π-A) measurements were used to characterize the effect of GlcCer on the biophysical properties of model membranes. We show that C16:0-GlcCer has a high tendency to segregate into highly ordered gel domains and to increase the order of the fluid phase. Monolayer studies support the aggregation propensity of C16:0-GlcCer. π-A isotherms of single C16:0-GlcCer indicate that bilayer domains, or crystal-like structures, coexist within monolayer domains at the air-water interface. Mixtures with POPC exhibit partial miscibility with expansion of the mean molecular areas relative to the additive behavior of the components. Moreover, C16:0-GlcCer promotes morphological alterations in lipid vesicles leading to formation of flexible tubule-like structures that protrude from the fluid region of the bilayer. These results support the hypothesis that alterations in membrane biophysical properties induced by GlcCer might be involved in its mechanism of action.
AB - Glucosylceramide (GlcCer), a relevant intermediate in the pathways of glycosphingolipid metabolism, plays key roles in the regulation of cell physiology. The molecular mechanisms by which GlcCer regulates cellular processes are unknown, but might involve changes in membrane biophysical properties and formation of lipid domains. In the present study, fluorescence spectroscopy, confocal microscopy and surface pressure-area (π-A) measurements were used to characterize the effect of GlcCer on the biophysical properties of model membranes. We show that C16:0-GlcCer has a high tendency to segregate into highly ordered gel domains and to increase the order of the fluid phase. Monolayer studies support the aggregation propensity of C16:0-GlcCer. π-A isotherms of single C16:0-GlcCer indicate that bilayer domains, or crystal-like structures, coexist within monolayer domains at the air-water interface. Mixtures with POPC exhibit partial miscibility with expansion of the mean molecular areas relative to the additive behavior of the components. Moreover, C16:0-GlcCer promotes morphological alterations in lipid vesicles leading to formation of flexible tubule-like structures that protrude from the fluid region of the bilayer. These results support the hypothesis that alterations in membrane biophysical properties induced by GlcCer might be involved in its mechanism of action.
UR - http://www.scopus.com/inward/record.url?scp=84872166522&partnerID=8YFLogxK
U2 - 10.1016/j.bbamem.2012.11.018
DO - 10.1016/j.bbamem.2012.11.018
M3 - مقالة
SN - 0005-2736
VL - 1828
SP - 1122
EP - 1130
JO - Biochimica Et Biophysica Acta-Biomembranes
JF - Biochimica Et Biophysica Acta-Biomembranes
IS - 3
ER -