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Bioactive TGF-beta can associate with lipoproteins and is enriched in those containing apolipoprotein E3.
- Source :
-
Journal of neurochemistry [J Neurochem] 2009 Aug; Vol. 110 (4), pp. 1254-62. Date of Electronic Publication: 2009 Jun 15. - Publication Year :
- 2009
-
Abstract
- Transforming growth factor-beta1 (TGF-beta1) has central functions in development, tissue maintenance, and repair and has been implicated in major diseases. We discovered that TGF-beta1 contains several amphipathic helices and hydrophobic domains similar to apolipoprotein E (apoE), a protein involved in lipoprotein metabolism. Indeed, TGF-beta1 associates with lipoproteins isolated from human plasma, cultured liver cells, or astrocytes, and its bioactivity was highest in high-density lipoprotein preparations. Importantly, lipoproteins containing the apoE3 isoform had higher TGF-beta levels and bioactivity than those containing apoE4, a major genetic risk factor for atherosclerosis and Alzheimer's disease. Because TGF-beta1 can be protective in these diseases an association with apoE3 may be beneficial. Association of TGF-beta with different types of lipoproteins may facilitate its diffusion, regulate signaling, and offer additional specificity for this important growth factor.
- Subjects :
- Animals
Apolipoprotein E3 genetics
Apolipoprotein E4 metabolism
Cell Line
Cells, Cultured
Humans
Lipid Metabolism physiology
Mice
Mice, Knockout
Protein Isoforms metabolism
Protein Structure, Secondary physiology
Protein Structure, Tertiary physiology
Signal Transduction physiology
Transforming Growth Factor beta1 chemistry
Transforming Growth Factor beta1 genetics
Apolipoprotein E3 metabolism
Astrocytes metabolism
Hepatocytes metabolism
Lipoproteins metabolism
Transforming Growth Factor beta1 metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1471-4159
- Volume :
- 110
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Journal of neurochemistry
- Publication Type :
- Academic Journal
- Accession number :
- 19549280
- Full Text :
- https://doi.org/10.1111/j.1471-4159.2009.06222.x