Abstract
Cell surface proteins containing covalently linked lipids associate with specialized membrane domains. Morphogens like Hedgehog and Wnt use their lipid anchors to bind to lipoprotein particles and employ lipoproteins to travel through tissues. Removal of their lipid anchors or decreasing lipoprotein levels give rise to adverse Hedgehog and Wnt signaling. Some parasites can also transfer their glycosylphosphatidylinositol-anchored surface proteins to host lipoprotein particles. These antigen-loaded lipoproteins spread throughout the circulation, and probably hamper an adequate immune response by killing neutrophils. Together, these findings imply a widespread role for lipoproteins in intercellular transfer of lipidanchored surface proteins, and may have various physiological consequences. Here,we discuss howlipid-modified proteins may be transferred to and fromlipoproteins at the cellular level.
| Original language | Undefined/Unknown |
|---|---|
| Pages (from-to) | 331-338 |
| Number of pages | 8 |
| Journal | Traffic |
| Volume | 8 |
| Publication status | Published - 2007 |