Loading...
Please wait, while we are loading the content...
Similar Documents
Heterotrimeric G proteins physically associated with the lipopolysaccharide receptor CD14 modulate both in vivo and in vitro responses to lipopolysaccharide.
| Content Provider | Semantic Scholar |
|---|---|
| Author | Kurt-Jones, Evelyn A. Dunn, Ian Frederick Ferretti, Massimo Golenbock, Douglas T. |
| Copyright Year | 1998 |
| Abstract | Septic shock induced by lipopolysaccharide (LPS) triggering of cytokine production from monocytes/macrophages is a major cause of morbidity and mortality. The major monocyte/macrophage LPS receptor is the glycosylphosphatidylinositol (GPI)-anchored glycoprotein CD14. Here we demonstrate that CD14 coimmunoprecipitates with Gi/Go heterotrimeric G proteins. Furthermore, we demonstrate that heterotrimeric G proteins specifically regulate CD14-mediated, LPS-induced mitogen-activated protein kinase (MAPK) activation and cytokine production in normal human monocytes and cultured cells. We report here that a G protein binding peptide protects rats from LPS-induced mortality, suggesting a functional linkage between a GPI-anchored receptor and the intracellular signaling molecules with which it is physically associated. |
| File Format | PDF HTM / HTML |
| Alternate Webpage(s) | http://dunnlab.bwh.harvard.edu/wp-content/uploads/2015/04/Solomon-1998-heterotrimeric-G-proteins-physically-associated-w-LPS-receptor-CD14-JCI.pdf |
| Alternate Webpage(s) | http://dm5migu4zj3pb.cloudfront.net/manuscripts/4000/4317/JCI9804317.pdf |
| PubMed reference number | 9835628v1 |
| Volume Number | 102 |
| Issue Number | 11 |
| Journal | The Journal of clinical investigation |
| Language | English |
| Access Restriction | Open |
| Subject Keyword | CD14 Antigen CELF Proteins Glycosylphosphatidylinositols Interleukin Receptor Common gamma Subunit Lipopolysaccharides Mitogen-Activated Protein Kinases Mitogens Monocytes Morbidity - disease rate Septic Shock cytokine production genetic linkage |
| Content Type | Text |
| Resource Type | Article |