4.6 Article

Gangliosides of the nuclear membrane: A crucial locus of cytoprotective modulation

Journal

JOURNAL OF CELLULAR BIOCHEMISTRY
Volume 97, Issue 5, Pages 893-903

Publisher

WILEY
DOI: 10.1002/jcb.20731

Keywords

gangliosides; nuclear membrane; nuclear calcium; sodium calcium exchanger; GM1-sodium calcium exchanger complex; cytoprotection by nuclear exchanger/GM1

Funding

  1. NINDS NIH HHS [2 R01 NS033912-08] Funding Source: Medline

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The original concept of gangliosides as localized components of the plasma membrane has broadened in recent years with recognition of their presence in various intracellular pools as well. The nuclear envelope (NE), consisting of two unique membranes, is one such structure shown to contain members of the gangliotetraose family and possibly other sialoglycolipids. GM1 Situated in the inner membrane of the NE is tightly associated with a Na+/Ca2+ exchanger whose activity it potentiates in the transfer of Ca2+ from nucleoplasm to the NE lumen. This is in contrast to Na+/Ca2+ exchangers of the plasma membrane which bind GM1 less avidly or not at all. This is believed due to different isoforms of exchanger, and a difference in topology of the exchanger relative to GM1. Cultured neurons from mice genetically engineered to lack gangliotetraose gangliosides such as GMI were highly vulnerable to Ca2+-induced apoptosis. They were rescued to some extent by GMI but more effectively by LIGA-20, a membrane-permeant derivative of GMI that traverses the plasma membrane more effectively than GMI and inserts into the NE. As further indication of Ca2+ dysregulation, the mutant mice were highly susceptible to kainite-induced seizures which were attenuated by LIGA-20. This correlated with the ability of LIGA-20 to cross the blood-brain barrier, enter brain cells, insert into the NE, and potentiate the nuclear exchanger. GM1 in the NE, in association with nuclear Na+/Ca2+ exchanger, is thus seen as contributing to Ca2+ regulation within the nucleus and in the process exerting a cytoprotective role.

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