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PMID: 14720509 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Sucrose-induced vacuolation results in increased expression of cholesterol biosynthesis and lysosomal genes.

Experimental cell research ·Vol. 292 ·No. 1 ·2004-01-01 ·Pages 89-100

Helip-Wooley A, Thoene JG

Abstract

Mammalian cells cultured in the presence of high concentrations of sucrose demonstrate large, phase-lucent, osmotically swollen vacuoles. Three normal human fibroblast cell lines exposed to 100 mM of sucrose for 24 h demonstrated increased expression of lysosomal, intracellular vesicle trafficking, cholesterol biosynthesis, and fatty acid metabolism genes. Most steps of the cholesterol biosynthesis pathway were upregulated including HMG CoA reductase, which catalyzes the rate-limiting step of cholesterol biosynthesis. The lysosomal genes neuraminidase, CLN3, and CLCN5 and the small GTP-binding proteins Rab7L1 and Arl7 were also increased. A Rab7L1-GFP fusion protein was overexpressed in human fibroblasts and was demonstrated to localize primarily to the Golgi apparatus, and in some cells to the membranes bounding vesicles in the perinuclear region. Increased levels of the transcription factor C/EBP were found in nuclear extracts from cells exposed to sucrose for 12 h, relative to matched controls suggesting regulation of gene expression following sucrose-induced vacuolation may be coordinated, at least in part, by the transcription factor C/EBP. Sucrose-induced vacuolation is a useful model in which to study the regulation of lysosomal gene expression and biogenesis.

MeSH Terms
Cell Extracts/chemistry Cell Line Cell Nucleus/chemistry Chloride Channels/drug effects,metabolism Cholesterol/biosynthesis,genetics,metabolism Fatty Acids/metabolism Fibroblasts/cytology,drug effects,metabolism Gene Expression Regulation Golgi Apparatus/metabolism Green Fluorescent Proteins Humans Luminescent Proteins/metabolism Lysosomes/drug effects,genetics,metabolism Membrane Glycoproteins Molecular Chaperones Neuraminidase/drug effects,metabolism Proteins/drug effects,metabolism RNA, Messenger/genetics,metabolism Recombinant Fusion Proteins/metabolism Sucrose/pharmacology Transcription Factors/genetics,metabolism Vacuoles/drug effects,metabolism rab GTP-Binding Proteins/drug effects,metabolism
Chemicals
CLC-5 chloride channel CLN3 protein, human Cell Extracts Chloride Channels Fatty Acids Luminescent Proteins Membrane Glycoproteins Molecular Chaperones Proteins RNA, Messenger Recombinant Fusion Proteins Transcription Factors Green Fluorescent Proteins Sucrose Cholesterol Neuraminidase rab GTP-Binding Proteins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Helip-Wooley Amanda
Hayward Human Genetics Center, Tulane University School of Medicine, New Orleans, LA 70112, USA. [email protected]
Thoene Jess G
Article Info
Journal
Experimental cell research
Abbr.
Exp Cell Res
ISSN
0014-4827
Published
2004-01-01
Pages
89-100
Language
English
Region
United States
NLM ID
0373226
Subset
IM
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