Sphingomyelinase-Mediated Multitimescale Clustering of Ganglioside GM1 in Heterogeneous Lipid Membranes

被引:5
作者
Lee, Hyun-Ro [1 ]
Choi, Siyoung Q. [1 ,2 ]
机构
[1] Korea Adv Inst Sci & Technol KAIST, Dept Chem & Biomol Engn, Daejeon 34141, South Korea
[2] Korea Adv Inst Sci & Technol KAIST, KAIST Inst NanoCentury, Daejeon 34141, South Korea
基金
新加坡国家研究基金会;
关键词
ceramides; GM1; gangliosides; lipid clustering; lipid membranes; membrane remodeling; sphingomyelinases; ACID SPHINGOMYELINASE; DISPLACES CHOLESTEROL; PLASMA-MEMBRANE; GIANT VESICLES; CERAMIDE; PHASE; DOMAINS; RAFTS; REORGANIZATION; SPHINGOLIPIDS;
D O I
10.1002/advs.202101766
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Several signaling processes in the plasma membrane are intensified by ceramides that are formed by sphingomyelinase-mediated hydrolysis of sphingomyelin. These ceramides trigger clustering of signaling-related biomolecules, but how they concentrate such biomolecules remains unclear. Here, the spatiotemporal localization of ganglioside GM1, a glycolipid receptor involved in signaling, during sphingomyelinase-mediated hydrolysis is described. Real-time visualization of the dynamic remodeling of the heterogeneous lipid membrane that occurs due to sphingomyelinase action is used to examine GM1 clustering, and unexpectedly, it is found that it is more complex than previously thought. Specifically, lipid membranes generate two distinct types of condensed GM1: 1) rapidly formed but short-lived GM1 clusters that are formed in ceramide-rich domains nucleated from the liquid-disordered phase; and 2) late-onset yet long-lasting, high-density GM1 clusters that are formed in the liquid-ordered phase. These findings suggest that multiple pathways exist in a plasma membrane to synergistically facilitate the rapid amplification and persistence of signals.
引用
收藏
页数:10
相关论文
共 83 条
[21]   Sphingolipids in apoptosis, survival and regeneration in the nervous system [J].
de Chaves, Elena I. Posse .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2006, 1758 (12) :1995-2015
[22]   Sphingolipids and gangliosides of the nervous system in membrane function and dysfunction [J].
de Chaves, Elena Posse ;
Sipione, Simonetta .
FEBS LETTERS, 2010, 584 (09) :1748-1759
[23]   Ceramide-lipid interactions studied by MD simulations and solid-state NMR [J].
Dutagaci, Bercem ;
Becker-Baldus, Johanna ;
Faraldo-Gomez, Jose D. ;
Glaubitz, Clemens .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2014, 1838 (10) :2511-2519
[24]   GM1 structure determines SV40-induced membrane invagination and infection [J].
Ewers, Helge ;
Roemer, Winfried ;
Smith, Alicia E. ;
Bacia, Kirsten ;
Dmitrieff, Serge ;
Chai, Wengang ;
Mancini, Roberta ;
Kartenbeck, Juergen ;
Chambon, Valerie ;
Berland, Ludwig ;
Oppenheim, Ariella ;
Schwarzmann, Guenter ;
Feizi, Ten ;
Schwille, Petra ;
Sens, Pierre ;
Helenius, Ari ;
Johannes, Ludger .
NATURE CELL BIOLOGY, 2010, 12 (01) :11-U36
[25]   Absence of fluid-ordered/fluid-disordered phase coexistence in ceramide/POPC mixtures containing cholesterol [J].
Fidorra, M. ;
Duelund, L. ;
Leidy, C. ;
Simonsen, A. C. ;
Bagatolli, L. A. .
BIOPHYSICAL JOURNAL, 2006, 90 (12) :4437-4451
[26]   PAF-mediated pulmonary edema:: a new role for acid sphingomyelinase and ceramide [J].
Göggel, R ;
Winoto-Morbach, S ;
Vielhaber, G ;
Imai, Y ;
Lindner, K ;
Brade, L ;
Brade, H ;
Ehlers, S ;
Slutsky, AS ;
Schütze, S ;
Gulbins, E ;
Uhlig, S .
NATURE MEDICINE, 2004, 10 (02) :155-160
[27]   Biophysics of sphingolipids I.: Membrane properties of sphingosine, ceramides and other simple sphingolipids [J].
Goni, Felix M. ;
Alonso, Alicia .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2006, 1758 (12) :1902-1921
[28]   Rhinoviruses infect human epithelial cells via ceramide-enriched membrane platforms [J].
Grassmé, H ;
Riehle, A ;
Wilker, B ;
Gulbins, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (28) :26256-26262
[29]   Ceramide-mediated clustering is required for CD95-DISC formation [J].
Grassmé, H ;
Cremesti, A ;
Kolesnick, R ;
Gulbins, E .
ONCOGENE, 2003, 22 (35) :5457-5470
[30]   Host defense against Pseudomonas aeruginosa requires ceramide-rich membrane rafts [J].
Grassmé, H ;
Jendrossek, V ;
Riehle, A ;
von Kürthy, G ;
Berger, J ;
Schwarz, H ;
Weller, M ;
Kolesnick, R ;
Gulbins, E .
NATURE MEDICINE, 2003, 9 (03) :322-330