Document Detail


Nuclear sphingomyelin pathway in serum deprivation-induced apoptosis of embryonic hippocampal cells.
MedLine Citation:
PMID:  16021626     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Sphingomyelin (SM) cycle has been involved in the regulation of proliferation, differentiation, and apoptosis. Increases in ceramide have been found after a larger number of apoptotic stimuli including cytokines, cytotoxic drugs, and environmental stresses. Accumulating evidence suggest that the subcellular localization of ceramide generation is a critical factor in determining the cellular behavior. Since recently enzymes involved in ceramide metabolism such as sphingomyelinase, SM synthase, sphingosine kinase and ceramidase have been found in the nucleus of hepatocyte cells, we have studied first the presence and the physicochemical characteristics of SM metabolism enzymes in nuclei isolated from embryonic hippocampal cells (cell line HN9.10e). The activities of sphingomyelinase and SM-synthase have been assayed and the ceramide production evaluated at different times after serum deprivation in these neurones cultivated in serum-deficient medium. We report that both enzymes are present in the nucleus of embryonic hippocampal cells and differ from those present in the homogenate in optimum pH. After serum deprivation, that induces a time-dependent decrease in cell viability and increase of the cell percentage in G1 phase of the cell cycle, a nuclear sphingomyelinase activation together with SM-synthase inhibition and a consequent increase of nuclear ceramide pool have been demonstrated. No similar enzyme activity modifications in homogenate have been identified. The possible role of nuclear sphingomyelinase/sphingomyelin-synthase balance in serum deprivation-induced apoptosis in the embryonic hippocampal cell is discussed.
Authors:
Elisabetta Albi; Samuela Cataldi; Elisa Bartoccini; Mariapia Viola Magni; Francesca Marini; Francesca Mazzoni; Giuseppe Rainaldi; Monica Evangelista; Mercedes Garcia-Gil
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Journal of cellular physiology     Volume:  206     ISSN:  0021-9541     ISO Abbreviation:  J. Cell. Physiol.     Publication Date:  2006 Jan 
Date Detail:
Created Date:  2005-11-03     Completed Date:  2006-03-17     Revised Date:  2007-11-15    
Medline Journal Info:
Nlm Unique ID:  0050222     Medline TA:  J Cell Physiol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  189-95     Citation Subset:  IM    
Copyright Information:
Copyright 2005 Wiley-Liss, Inc.
Affiliation:
Department of Clinic and Experimental Medicine, Physiopathology, Policlinico Monteluce, Perugia, Italy.
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MeSH Terms
Descriptor/Qualifier:
Animals
Apoptosis / physiology*
Cell Cycle / physiology
Cell Nucleus / chemistry,  enzymology*
Cell Survival
Cells, Cultured
Culture Media / chemistry*
Embryo, Mammalian / anatomy & histology*
Embryo, Nonmammalian*
Hippocampus / cytology*
Neurons / cytology,  metabolism
Serum / metabolism*
Sphingomyelin Phosphodiesterase / metabolism
Sphingomyelins / metabolism*
Transferases (Other Substituted Phosphate Groups) / metabolism
Chemical
Reg. No./Substance:
0/Culture Media; 0/Sphingomyelins; EC 2.7.8.-/Transferases (Other Substituted Phosphate Groups); EC 2.7.8.-/phosphatidylcholine-ceramide phosphocholine transferase; EC 3.1.4.12/Sphingomyelin Phosphodiesterase

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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