期刊论文详细信息
International Journal of Molecular Sciences
Nuclear Lipid Microdomain as Place of Interaction between Sphingomyelin and DNA during Liver Regeneration
Elisabetta Albi1  Andrea Lazzarini2  Remo Lazzarini1  Alessandro Floridi1  Eleni Damaskopoulou1  Francesco Curcio2 
[1] Laboratory of Nuclear Lipid BioPathology, Research Center of Biochemical-Specialized Analyses, 06100 Perugia, Italy; E-Mails:;Department of Clinical and Biological Sciences, University of Udine, 33100 Udine, Italy; E-Mails:
关键词: nucleus;    nuclear lipid microdomains;    sphingomyelin;    sphingomyelinase;    sphingomyelin-synthase;    cell proliferation;   
DOI  :  10.3390/ijms14046529
来源: mdpi
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【 摘 要 】

Nuclear sphingomyelin is a key molecule for cell proliferation. This molecule is organized with cholesterol and proteins to form specific lipid microdomains bound to the inner nuclear membrane where RNA is synthesized. Here, we have reported the ability of the sphingomyelin present in the nuclear microdomain to bind DNA and regulate its synthesis, and to highlight its role in cell proliferation induced by partial hepatectomy. During G1/S transition of the cell cycle, sphingomyelin and DNA content is very high and it is strongly reduced after exogenous sphingomyelinase treatment. During the S-phase of the cell cycle, the stimulation of sphingomyelinase and inhibition of sphingomyelin–synthase are accompanied by the DNA synthesis start. To assess the specificity of the results, experiments were repeated with trifluoperazine, a drug known to affect the synthesis of lipids and DNA and to stimulate sphingomyelinase activity. The activity of sphingomyelinase is stimulated in the first hour after hepatectomy and sphingomyelin–DNA synthesis is strongly attenuated. It may be hypothesized that the nuclear microdomain represents a specific area of the inner nuclear membrane that acts as an active site of chromatin anchorage thanks to the stabilizing action of sphingomyelin. Thus, sphingomyelin metabolism in nuclear lipid microdomains is suggested to regulate cell proliferation.

【 授权许可】

CC BY   
© 2013 by the authors; licensee MDPI, Basel, Switzerland

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