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1.
Eur J Immunol ; 27(6): 1522-9, 1997 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-9209506

RESUMEN

The biological effects of the potent inflammatory mediator C5a, a complement split product, on human neutrophils and monocytes are limited by the rapid internalization of its specific receptor (C5aR, CD88). The C terminus of the C5aR is phosphorylated after stimulation with C5a of phorbol ester, and this phosphorylation might lead to receptor internalization. In this context, we have studied the effects on C5aR internalization of C5a, phorbol 12-myristate 13-acetate (PMA), the protein kinase inhibitor staurosporine, and pertussis toxin on rat basophilic RBL.2H3 cells stably transfected with the human wild-type or mutant C5aR. C5aR mutants lacked either part of the cytosolic C terminus, including suggested major phosphorylation sites, or a putative phosphorylation motif for protein kinase C in the third cytosolic loop. Additionally, agonist-induced internalization was analyzed on HEK293 cells co-transfected with C5aR and the pertussis toxin-resistant G protein alpha subunit, G alpha 16. Staurosporine-sensitive agonist-dependent C5aR internalization could be detected, suggesting that C5aR phosphorylation, most likely of the C terminus, participates in this type of internalization. In contrast, PMA-induced C5aR internalization seems to be independent of putative phosphorylation sites in either the truncated section of the C terminus or the third cytosolic loop. The phorbol ester-induced C5aR internalization may, therefore, be caused by an indirect and less specific effect of protein kinase C on the internalization machinery. Manipulation of the pertussis toxin-sensitive or -resistant G protein-dependent signal transduction had no effect on ligand-induced internalization.


Asunto(s)
Antígenos CD/metabolismo , Antígenos CD/fisiología , Complemento C5a/metabolismo , Receptores de Complemento/metabolismo , Receptores de Complemento/fisiología , Animales , Antígenos CD/genética , Línea Celular , ADN Complementario/genética , Proteínas de Unión al GTP/efectos de los fármacos , Proteínas de Unión al GTP/genética , Humanos , Radioisótopos de Yodo , Riñón/citología , Riñón/embriología , Leucemia Basofílica Aguda/metabolismo , Ligandos , Mutagénesis Sitio-Dirigida , Fragmentos de Péptidos/farmacología , Toxina del Pertussis , Unión Proteica , Inhibidores de Proteínas Quinasas , Ratas , Receptor de Anafilatoxina C5a , Receptores de Complemento/genética , Estaurosporina/farmacología , Acetato de Tetradecanoilforbol/farmacología , Transfección , Células Tumorales Cultivadas , Factores de Virulencia de Bordetella/agonistas
2.
Br J Clin Pract ; 48(6): 332-3, 1994.
Artículo en Inglés | MEDLINE | ID: mdl-7848800

RESUMEN

We report the case of an Asian woman who was exposed to toxic levels of lead, arsenic and mercury through the use of Indian ethnic remedies, and who suffered symptomatic lead poisoning. We know of no other case of exposure to such a combination of heavy metals from this source. We believe that control of the dispensing of these compounds is essential.


Asunto(s)
Intoxicación por Arsénico , Intoxicación por Plomo/etiología , Medicina Tradicional , Intoxicación por Mercurio/etiología , Femenino , Humanos , India , Persona de Mediana Edad
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