RESUMEN
Available data on the existence of lentivirus proteins with properties of unconventional Ag for B cells, have been so far restricted to human immunodeficiency virus (i.e. gp-120 of HIV-I). By using biotinylated-MAbs-anti-biotin IgG as readout system, we now report that gag-p24 antigen, either assembled in feline immunodeficiency virus (FIV) particles or expressed as recombinant polypeptide (rec.p24) may bind to nonimmune IgGs purified from mouse or cat sera. Moreover, FACS scanning experiments are consistent with the possibility that rec.p24 interacts with surface-Ig in a sub-population (5-6%) of rodent B cells. We hypothesize that gag-p24 peptide encoded regions may bind to unconventional Ig sites or, alternatively, that they may represent 'public' epitopes for natural polyreactive antibody.
Asunto(s)
Productos del Gen gag/inmunología , Virus de la Inmunodeficiencia Felina/inmunología , Inmunoglobulinas/inmunología , Péptidos/inmunología , Animales , Gatos , Ratones , Ratones Endogámicos BALB C , Proteínas Recombinantes de Fusión/inmunologíaRESUMEN
Trop-2/EGP-1/GA733-1 is a recently identified cell surface glycoprotein highly expressed by human carcinomas. The cytoplasmic tail of Trop-2 possesses potential serine and tyrosine phosphorylation sites and a phosphatidyl-inositol binding consensus sequence. Thus, we investigated whether Trop-2 might be a functional signaling molecule. Using the fluorescent probe Fura-2, we assayed the cytoplasmic calcium levels in human cancer cells stimulated with anti-Trop-2 or control antibodies. Three anti-Trop-2 MAbs, Rs7-7G11, MOv16 and 162-46.2 specifically induced a transient intracellular calcium level increment in up to 40% of the experiments performed. Polyclonal antisera recognizing recombinant Trop-2 molecules possessed a much lower stimulation efficiency. The average latency of antibody-induced Ca2+ rise for OvCa-432 cells was 64+/-26 sec. Internal Ca2+ concentrations reached peaks of 190+/-24 nM vs. basal levels of 61+/-4 nM and returned to baseline within 193+/-37 sec. Similar values were obtained in MCF-7 cells. For comparison, stimulation of P2-purinergic receptors on MCF-7 and OvCa-432 cells induced a Ca2+ rise in most cases, leading to average internal Ca2+ concentrations of 297+/-41 and 391+/-39 nM, respectively. Our findings show that Trop-2 transduces an intracellular calcium signal, are consistent with the hypothesis that it acts as a cell surface receptor and support a search for a physiological ligand.
Asunto(s)
Antígenos de Neoplasias/fisiología , Antígenos de Superficie/fisiología , Neoplasias de la Mama/metabolismo , Calcio/metabolismo , Moléculas de Adhesión Celular , Glicoproteínas de Membrana/fisiología , Neoplasias Ováricas/metabolismo , Transducción de Señal/fisiología , Adenosina Trifosfato/farmacología , Adenosina Trifosfato/fisiología , Animales , Anticuerpos Monoclonales/farmacología , Especificidad de Anticuerpos , Antígenos de Neoplasias/farmacología , Antígenos de Superficie/farmacología , Neoplasias de la Mama/patología , Adhesión Celular/fisiología , Citosol/fisiología , Molécula de Adhesión Celular Epitelial , Femenino , Citometría de Flujo , Humanos , Inmunoconjugados/farmacología , Glicoproteínas de Membrana/farmacología , Ratones , Neoplasias Ováricas/patología , Proteínas Recombinantes/farmacología , Transducción de Señal/efectos de los fármacos , Células Tumorales CultivadasRESUMEN
Anti-10 deacetylbaccatin III (DAB) antibodies (IgY) were elicited in hens immunized with a succinyl-DAB/BSA conjugate and extracted from egg yolk. As shown by indirect competitive inhibition enzyme immunoassay (CIEIA), the addition of free-DAB competitively inhibited the binding of affinity purified anti-DAB IgY to DAB/BSA solid phase conjugated antigen. The assay enabled the detection of DAB in concentrations as low as 7.5ng/ml (13.7 nM DAB), whereas anti-DAB IgY did not react with taxol even at a concentration a thousand times higher. The structural requirements of the diterpenoid nucleus for binding to IgY were considered on the basis of the levels of cross-reaction found with 10 authentic taxanes. The results indicate that anti-DAB IgY represents the first high affinity antibody produced capable of recognizing the ring skeleton of taxol precursors.