Analysis of C5a-mediated chemotaxis by lentiviral delivery of small interfering RNA
AUTOR(ES)
Hwang, Jong-Ik
FONTE
National Academy of Sciences
RESUMO
Immune cells respond to chemotactic signals by means of G protein-coupled receptors. Attempts to elucidate the function of specific G protein family members in these responses is complicated by redundancy among the different G protein isoforms. We have used lentiviral-based RNA interference to eliminate expression of specific G protein subunits selectively in J774A.1 mouse macrophages. The chemotactic response to the complement factors C5a and C3a is ablated in cells lacking Gβ2 but is unaffected in cells lacking Gβ1, Gαi2, or Gαi3. Similarly, the C5a-mediated calcium response of single cells is either absent or significantly delayed and weakened by Gβ2 knockdown. Assessment of Akt1 phosphorylation levels in response to C5a shows rapid and sustained phosphorylation in both wild-type cells and cells lacking Gβ1. Cells lacking Gβ2 retain the rapid response but cannot sustain phospho-Akt1 levels. The phenotype of cells lacking Gβ2 can be reversed by overexpression of either human Gβ2 or mouse Gβ1. These data demonstrate the usefulness of lentiviral-based RNA interference in the systematic analysis of a signaling pathway, and they suggest that in J774A.1 cells, Gβ2-derived Gβγ is the most effective mediator of chemotaxis to C5a.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=327174Documentos Relacionados
- Inhibiting HIV-1 infection in human T cells by lentiviral-mediated delivery of small interfering RNA against CCR5
- A general method for gene knockdown in mice by using lentiviral vectors expressing small interfering RNA
- Retroviral delivery of small interfering RNA into primary cells
- Atelocollagen-mediated synthetic small interfering RNA delivery for effective gene silencing in vitro and in vivo
- Small Interfering RNA-Mediated Inhibition of Hepatitis C Virus Replication in the Human Hepatoma Cell Line Huh-7
