Segregation of GM1 and GM3 clusters in the cell membrane depends on the intact actin cytoskeleton
- PMID: 19830910
- DOI: 10.1016/j.bbalip.2009.01.008
Segregation of GM1 and GM3 clusters in the cell membrane depends on the intact actin cytoskeleton
Abstract
Gangliosides have been implicated in exerting multiple physiological functions, and it is important to understand how their distribution is regulated in the cell membrane. By using freeze-fracture immunolabeling electron microscopy, we showed that GM1 and GM3 make independent clusters that are significantly reduced by cholesterol depletion. In the present study, we examined the effects of actin depolymerization/polymerization and Src-family kinase inhibition on the GM1 and GM3 clusters. Both GM1 and GM3 clustering was reduced when the actin cytoskeleton was perturbed by latrunculin A or jasplakinolide, but the decrease was less significant than that induced by cholesterol depletion. On the other hand, inhibition of Src-family kinases decreased GM3 clustering more drastically than did cholesterol depletion, whereas its effect on GM1 clustering was less significant. GM1 and GM3 were segregated from each other in unperturbed cells, but co-clustering increased significantly after actin depolymerization. Our results indicate that the GM1 and GM3 clusters in the cell membrane are regulated in different ways and that segregation of the two gangliosides depends on the intact actin cytoskeleton.
Similar articles
-
Gangliosides GM1 and GM3 in the living cell membrane form clusters susceptible to cholesterol depletion and chilling.Mol Biol Cell. 2007 Jun;18(6):2112-22. doi: 10.1091/mbc.e07-01-0071. Epub 2007 Mar 28. Mol Biol Cell. 2007. PMID: 17392511 Free PMC article.
-
Rapid internalization of exogenous ganglioside GM3 and its metabolism to ceramide in human myelogenous leukemia HL-60 cells compared with control ganglioside GM1.FEBS Lett. 1997 Jan 6;400(3):350-4. doi: 10.1016/s0014-5793(96)01415-9. FEBS Lett. 1997. PMID: 9009229
-
Mechanistic study of modulation of SR Ca2+-ATPpase activity by gangliosides GM1 and GM3 through some biophysical measurements.Glycoconj J. 1999 Dec;16(12):781-6. doi: 10.1023/a:1007123714104. Glycoconj J. 1999. PMID: 11133018
-
Regulation of signal transduction by gangliosides in lipid rafts: focus on GM3-IR and GM1-TrkA interactions.FEBS Lett. 2022 Dec;596(24):3124-3132. doi: 10.1002/1873-3468.14532. Epub 2022 Nov 11. FEBS Lett. 2022. PMID: 36331354 Review.
-
Development of new ganglioside probes and unraveling of raft domain structure by single-molecule imaging.Biochim Biophys Acta Gen Subj. 2017 Oct;1861(10):2494-2506. doi: 10.1016/j.bbagen.2017.07.012. Epub 2017 Jul 20. Biochim Biophys Acta Gen Subj. 2017. PMID: 28734966 Review.
Cited by
-
Current approaches to studying membrane organization.F1000Res. 2015 Nov 30;4:F1000 Faculty Rev-1380. doi: 10.12688/f1000research.6868.1. eCollection 2015. F1000Res. 2015. PMID: 26918150 Free PMC article. Review.
-
The nanoscale organization of the B lymphocyte membrane.Biochim Biophys Acta. 2015 Apr;1853(4):830-40. doi: 10.1016/j.bbamcr.2014.11.010. Epub 2014 Nov 15. Biochim Biophys Acta. 2015. PMID: 25450974 Free PMC article. Review.
-
Interleaflet Coupling, Pinning, and Leaflet Asymmetry-Major Players in Plasma Membrane Nanodomain Formation.Front Cell Dev Biol. 2017 Jan 10;4:155. doi: 10.3389/fcell.2016.00155. eCollection 2016. Front Cell Dev Biol. 2017. PMID: 28119914 Free PMC article. Review.
-
Expressed glycosylphosphatidylinositol-anchored horseradish peroxidase identifies co-clustering molecules in individual lipid raft domains.PLoS One. 2014 Mar 26;9(3):e93054. doi: 10.1371/journal.pone.0093054. eCollection 2014. PLoS One. 2014. PMID: 24671047 Free PMC article.
-
The distribution of phosphatidylinositol 4,5-bisphosphate in acinar cells of rat pancreas revealed with the freeze-fracture replica labeling method.PLoS One. 2011;6(8):e23567. doi: 10.1371/journal.pone.0023567. Epub 2011 Aug 15. PLoS One. 2011. PMID: 21858170 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Miscellaneous