Nejvíce citovaný článek - PubMed ID 11809740
A novel lipid raft-associated glycoprotein, TEC-21, activates rat basophilic leukemia cells independently of the type 1 Fc epsilon receptor
Chemotaxis, a process leading to movement of cells toward increasing concentrations of chemoattractants, is essential, among others, for recruitment of mast cells within target tissues where they play an important role in innate and adaptive immunity. Chemotaxis is driven by chemoattractants, produced by various cell types, as well as by intrinsic cellular regulators, which are poorly understood. In this study we prepared a new mAb specific for the tetraspanin CD9. Binding of the antibody to bone marrow-derived mast cells triggered activation events that included cell degranulation, Ca(2+) response, dephosphorylation of ezrin/radixin/moesin (ERM) family proteins, and potent tyrosine phosphorylation of the non-T cell activation linker (NTAL) but only weak phosphorylation of the linker for activation of T cells (LAT). Phosphorylation of the NTAL was observed with whole antibody but not with its F(ab)(2) or Fab fragments. This indicated involvement of the Fcγ receptors. As documented by electron microscopy of isolated plasma membrane sheets, CD9 colocalized with the high-affinity IgE receptor (FcεRI) and NTAL but not with LAT. Further tests showed that both anti-CD9 antibody and its F(ab)(2) fragment inhibited mast cell chemotaxis toward antigen. Experiments with bone marrow-derived mast cells deficient in NTAL and/or LAT revealed different roles of these two adaptors in antigen-driven chemotaxis. The combined data indicate that chemotaxis toward antigen is controlled in mast cells by a cross-talk among FcεRI, tetraspanin CD9, transmembrane adaptor proteins NTAL and LAT, and cytoskeleton-regulatory proteins of the ERM family.
- MeSH
- adaptorové proteiny signální transdukční metabolismus MeSH
- antigeny CD9 fyziologie MeSH
- antigeny CD98 - lehké řetězce metabolismus MeSH
- antigeny metabolismus MeSH
- biologické modely MeSH
- buněčná membrána metabolismus MeSH
- chemotaxe MeSH
- cytoskelet metabolismus MeSH
- fosfoproteiny metabolismus MeSH
- fosforylace MeSH
- glukuronidasa metabolismus MeSH
- imunoglobuliny - Fab fragmenty chemie MeSH
- krysa rodu Rattus MeSH
- mastocyty cytologie MeSH
- membránové proteiny metabolismus MeSH
- myši inbrední C57BL MeSH
- myši MeSH
- potkani Wistar MeSH
- receptory IgE metabolismus MeSH
- transportní systém aminokyselin y+ metabolismus MeSH
- tyrosin chemie MeSH
- vápník metabolismus MeSH
- vazba proteinů MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- adaptorové proteiny signální transdukční MeSH
- antigeny CD9 MeSH
- antigeny CD98 - lehké řetězce MeSH
- antigeny MeSH
- fosfoproteiny MeSH
- glukuronidasa MeSH
- imunoglobuliny - Fab fragmenty MeSH
- Lat protein, mouse MeSH Prohlížeč
- Lat protein, rat MeSH Prohlížeč
- membránové proteiny MeSH
- receptory IgE MeSH
- SLC7A8 protein, mouse MeSH Prohlížeč
- Slc7a8 protein, rat MeSH Prohlížeč
- transportní systém aminokyselin y+ MeSH
- tyrosin MeSH
- vápník MeSH