DISP3, a sterol-sensing domain-containing protein that links thyroid hormone action and cholesterol metabolism
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
19179482
PubMed Central
PMC5419274
DOI
10.1210/me.2008-0271
PII: me.2008-0271
Knihovny.cz E-resources
- MeSH
- Cell Line MeSH
- Cholesterol metabolism MeSH
- Endoplasmic Reticulum metabolism MeSH
- Phylogeny MeSH
- Thyroid Hormones metabolism MeSH
- Chick Embryo MeSH
- Humans MeSH
- Membrane Proteins classification genetics metabolism MeSH
- Molecular Sequence Data MeSH
- Receptors, Thyroid Hormone genetics metabolism MeSH
- Gene Expression Regulation MeSH
- Recombinant Fusion Proteins genetics metabolism MeSH
- Tissue Distribution MeSH
- Animals MeSH
- Check Tag
- Chick Embryo MeSH
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Cholesterol MeSH
- DISP3 protein, human MeSH Browser
- Thyroid Hormones MeSH
- Membrane Proteins MeSH
- Receptors, Thyroid Hormone MeSH
- Recombinant Fusion Proteins MeSH
In the body, the brain is the most cholesterol-rich organ. Despite this, remarkably little is known about the mechanisms in the brain that regulate cholesterol homeostasis. Due to the blood-brain barrier, plasma lipoproteins are unable to traverse, and instead cholesterol must be synthesized de novo from within the central nervous system. Thyroid hormone receptors, activated in response to thyroid hormone (T(3)), are known to modulate the level of serum cholesterol via complex regulatory pathways. By screening for T(3)-regulated genes we have identified Disp3, a sterol-sensing domain-containing protein that is related to the Dispatched family of proteins. Analysis by RT-PCR and immunohistochemistry demonstrated that DISP3 is predominately expressed in specific cell types of the brain, retina, and testis. Using the model of hyperthyroidism in vivo, we observed the modulation of Disp3 expression in the retina. Furthermore, in vitro analysis of Disp3 expression in cells treated with T(3) revealed both positive and negative regulation. DISP3 localizes within the endoplasmic reticulum and was further found to colocalize with cholesterol. Ectopic expression of DISP3 in fibroblasts resulted in elevated cholesterol levels combined with an altered cholesterol distribution. Given that DISP3 is highly expressed in Purkinje cells, hippocampal neurons, and retinal ganglion cells and that its overexpression results in increased cholesterol levels, it is tempting to postulate that DISP3 may contribute to cholesterol homeostasis in neural cell types. Taken together, we propose that DISP3 represents a new molecular link between thyroid hormone and cholesterol metabolism.
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