Literature DB >> 9767101

Natural forms of shed tumor gangliosides.

Y Kong1, R Li, S Ladisch.   

Abstract

Gangliosides shed by tumor cells are immunosuppressive molecules, but the mechanisms of shedding are poorly understood. We therefore conducted a comprehensive study of shedding to identify the natural forms of shed gangliosides. By chemical detection and mass spectrometric analysis of the gangliosides of YAC-1 murine lymphoma cells, we first confirmed that all major ganglioside species are released. Then, by the combination of metabolic and cell surface radiolabeling, we further demonstrated that gangliosides are released directly from the cell plasma membrane, i.e. by shedding. Ultracentrifugation separated the conditioned medium of metabolically radiolabeled cells cultured in either serum-free or serum-containing medium into: (1) a pellet of 100-200 nm membrane vesicles (visualized by electron microscopy) containing nearly one-third of total shed gangliosides; and (2) the supernatant, which contained soluble gangliosides (two-thirds of the total shed gangliosides). Although the ganglioside concentration in the conditioned medium (6-14x10-8 M) was above the critical micelle concentration of purified YAC-1 gangliosides (<1x10-8 M), by gel filtration >90% of the soluble gangliosides were found in monomeric form (MW <2 kDa) and only <10% in micelles (130 kDa). Ultrafiltration of fresh conditioned medium likewise showed the existence of monomers, and the findings were confirmed in human Daoy medulloblastoma and mouse MEB4 melanoma cells. Thus, in their natural states, shed tumor cell gangliosides exist in three forms: membrane vesicles, micelles, and monomers.

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Year:  1998        PMID: 9767101     DOI: 10.1016/s0005-2760(98)00096-4

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  10 in total

1.  3'-Azidothymidine significantly alters glycosphingolipid synthesis in melanoma cells and decreases the shedding of gangliosides.

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Journal:  Glycoconj J       Date:  1999-03       Impact factor: 2.916

2.  Gangliosides of myelosupportive stroma cells are transferred to myeloid progenitors and are required for their survival and proliferation.

Authors:  Ana L Ziulkoski; Cláudia M B Andrade; Pilar M Crespo; Elisa Sisti; Vera M T Trindade; Jose L Daniotti; Fátima C R Guma; Radovan Borojevic
Journal:  Biochem J       Date:  2006-02-15       Impact factor: 3.857

Review 3.  Measuring brain lipids.

Authors:  Glyn Dawson
Journal:  Biochim Biophys Acta       Date:  2015-02-18

4.  Renal cell carcinoma-derived gangliosides suppress nuclear factor-kappaB activation in T cells.

Authors:  R G Uzzo; P Rayman; V Kolenko; P E Clark; M K Cathcart; T Bloom; A C Novick; R M Bukowski; T Hamilton; J H Finke
Journal:  J Clin Invest       Date:  1999-09       Impact factor: 14.808

5.  Influence of gangliosides on the IL-2- and IL-4-dependent cell proliferation.

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Journal:  Neurochem Res       Date:  2002-08       Impact factor: 3.996

Review 6.  Deregulated sphingolipid metabolism and membrane organization in neurodegenerative disorders.

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Journal:  Mol Neurobiol       Date:  2010-02-03       Impact factor: 5.590

Review 7.  Signaling defects in anti-tumor T cells.

Authors:  Alan B Frey; Ngozi Monu
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8.  Inhibition of glycolipid shedding rescues recognition of a CD1+ T cell lymphoma by natural killer T (NKT) cells.

Authors:  Venkataraman Sriram; Sungyoo Cho; Ping Li; Patrick W O'Donnell; Claire Dunn; Kyoko Hayakawa; Janice S Blum; Randy R Brutkiewicz
Journal:  Proc Natl Acad Sci U S A       Date:  2002-06-11       Impact factor: 11.205

9.  The function of cancer-shed gangliosides in macrophage phenotype: involvement with angiogenesis.

Authors:  Tae-Wook Chung; Hee-Jung Choi; Mi-Ju Park; Hee-Jin Choi; Syng-Ook Lee; Keuk-Jun Kim; Cheorl-Ho Kim; Changwan Hong; Kyun-Ha Kim; Myungsoo Joo; Ki-Tae Ha
Journal:  Oncotarget       Date:  2017-01-17

10.  Proteome profiling of neuroblastoma-derived exosomes reveal the expression of proteins potentially involved in tumor progression.

Authors:  Danilo Marimpietri; Andrea Petretto; Lizzia Raffaghello; Annalisa Pezzolo; Cristina Gagliani; Carlo Tacchetti; Pierluigi Mauri; Giovanni Melioli; Vito Pistoia
Journal:  PLoS One       Date:  2013-09-19       Impact factor: 3.240

  10 in total

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