| Literature DB >> 19549280 |
Ina Tesseur1, Hui Zhang, Walter Brecht, Jacob Corn, Jian-Sheng Gong, Katsuhiko Yanagisawa, Makoto Michikawa, Karl Weisgraber, Yadong Huang, Tony Wyss-Coray.
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.Entities:
Mesh:
Substances:
Year: 2009 PMID: 19549280 PMCID: PMC2915937 DOI: 10.1111/j.1471-4159.2009.06222.x
Source DB: PubMed Journal: J Neurochem ISSN: 0022-3042 Impact factor: 5.372