Transmembrane signalling associated with ganglioside-induced CD4 modulation
1990
Abstract Ganglioside (GM 1 ) treatment of CD4 + human CEM ltmphoma cells stimulated transient phosphoinositide (PI) breakdown, production of inositol phosphates (IP), protein phosphorylation and rapid decrease of CD4 surface expression. A comparison between the actions of GM 1 and other agents that affect these signal transduction pathways demonstrated a distinct mechanism for GM 1 -induced decrease of CD4. GM 1 stimulated both phospholipase C activity and protein phosphorylation but had no effect on either cellular cAMP levels or tyrosine kinase activity. Phorbol myristate acetate (PMA) stimulated protein phosphorylation and caused a significant decrease in surface display of CD4. Both of these processes were blocked by pretreating cells with the protein kinase C (PKC) inhibitor H7. These results demonstrate that GM 1 stimulates PI turnover and induces a rapid decrease of CD4 surface expression by processes that do not activate adenylate cyclase or tyrosine kinase. They further demonstrate that the mechanism for GM 1 -induced decrease of CD4 is distinct from the CD4 internalization processes mediated by PKC activity.
Keywords:
- Correction
- Source
- Cite
- Save
- Machine Reading By IdeaReader
29
References
11
Citations
NaN
KQI