Skip Navigation

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (56)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Gillard, B. K.
Right arrow Articles by Marcus, D. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Gillard, B. K.
Right arrow Articles by Marcus, D. M.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Glycobiology vol 3 no 1 pp. 57-67, 1993
© 1993


research-article

Variable subcellular localization of glycosphingolipids

Baiba K. Gillard1, Lisa T. Thurmon1 and Donald M. Marcus1,2

1Departments of Medicine, Baylor College of Medicine Houston, TX 77030, USA
2Departments of Microbiology and Immunology, Baylor College of Medicine Houston, TX 77030, USA


Received on September 9, 1992; accepted on November 11, 1992

Although most glycosphingolipids (GSLs) are thought to be located in the outer leaflet of the plasma membrane, recent evidence indicates that GSLs are also associated with intracellular organelles. We now report that the subcellular localization of GSLs varies depending on the GSL structure and cell type. GSL localization was determined by indirect immunofluorescence microscopy of fixed permeabilized cells. A single GSL exhibited variable subcellular localization in different cells. For example, antibody to GalCer is localized primarily to the plasma membrane of HaCaT II-3 keratinocytes, but to intracellular organelies in other epithelial cells. GalCer is localized to small vesicles and tubulovesicular structures in MDCK cells, and to the surface of phase-dense lipid droplets in HepG2 hepatoma cells. Furthermore, within a single cell type, individual GSLs were found to exhibit different patterns of subcellular localization. In HepG2 cells, LacCer was associated with small vesicles, which differed from the phase-dense vesicles stained by anti-GalCer, and Gb4Cer was associated with the intermediate filaments of the cytoskeleton. Both anti-GalCer and monoclonal antibody A2B5, which binds polysialogangliosides, localized to mitochondria. The distinct subcellular localization patterns of GSLs raise interesting questions about their functions in different organelles. Together with published data on the enrichment of GSLs in specific organelles and in apical plasma membrane, these findings indicate the existence of specific sorting mechanisms that regulate the intracellular transport and localization of GSLs.

cytoskeleton glycosphingolipid intracellular organelles mitochondria subcellular localization


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
L. M. G. Chavas, C. Tringali, P. Fusi, B. Venerando, G. Tettamanti, R. Kato, E. Monti, and S. Wakatsuki
Crystal Structure of the Human Cytosolic Sialidase Neu2: EVIDENCE FOR THE DYNAMIC NATURE OF SUBSTRATE RECOGNITION
J. Biol. Chem., January 7, 2005; 280(1): 469 - 475.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
L. Kolesnikova, B. Berghofer, S. Bamberg, and S. Becker
Multivesicular Bodies as a Platform for Formation of the Marburg Virus Envelope
J. Virol., November 15, 2004; 78(22): 12277 - 12287.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
S. Tagami, J.-i. Inokuchi, K. Kabayama, H. Yoshimura, F. Kitamura, S. Uemura, C. Ogawa, A. Ishii, M. Saito, Y. Ohtsuka, et al.
Ganglioside GM3 Participates in the Pathological Conditions of Insulin Resistance
J. Biol. Chem., January 25, 2002; 277(5): 3085 - 3092.
[Abstract] [Full Text] [PDF]


Home page
J. Histochem. Cytochem.Home page
N. Kovacic, J. Müthing, and A. Marusic
Immunohistological and Flow Cytometric Analysis of Glycosphingolipid Expression in Mouse Lymphoid Tissues
J. Histochem. Cytochem., December 1, 2000; 48(12): 1677 - 1690.
[Abstract] [Full Text]


Home page
Cancer Res.Home page
R. Chammas, J. L. Sonnenburg, N. E. Watson, T. Tai, M. G. Farquhar, N. M. Varki, and A. Varki
De-N-acetyl-gangliosides in Humans: Unusual Subcellular Distribution of a Novel Tumor Antigen
Cancer Res., March 1, 1999; 59(6): 1337 - 1346.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
S Goletz, F. Hanisch, and U Karsten
Novel alphaGalNAc containing glycans on cytokeratins are recognized invitro by galectins with type II carbohydrate recognition domains
J. Cell Sci., January 7, 1997; 110(14): 1585 - 1596.
[Abstract] [PDF]


Home page
J. Biol. Chem.Home page
M. Hara-Yokoyama, Y. Hirabayashi, F. Irie, B. Syuto, K. Moriishi, H. Sugiya, and S. Furuyama
Identification of Gangliosides as Inhibitors of ADP-ribosyltransferases of Pertussis Toxin and Exoenzyme C3 from Clostridium botulinum
J. Biol. Chem., April 7, 1995; 270(14): 8115 - 8121.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
B. Gillard, L. Thurmon, R. Harrell, Y Capetanaki, M Saito, R. Yu, and D. Marcus
Biosynthesis of glycosphingolipids is reduced in the absence of a vimentin intermediate filament network
J. Cell Sci., January 12, 1994; 107(12): 3545 - 3555.
[Abstract] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.