CERELA   05438
CENTRO DE REFERENCIA PARA LACTOBACILOS
Unidad Ejecutora - UE
congresos y reuniones científicas
Título:
DISRUPTION OF LIPID RAFTS MODIFIES THE SECRETED CYTOKINES PROFILE INTO THE CULTURE MEDIUM BY PERIPHERAL BLOOD MONONUCLEAR CELLS STIMULATED WITH Lactobacillus acidophilus CRL 1014.
Autor/es:
G.E. JUAREZ, M.A. MECHOUD, G. FONT DE VALDEZ, A.V. RODRIGUEZ.
Lugar:
San Miguel de Tucumán
Reunión:
Simposio; III Simposio Internacional de Bacterias Lácticas. Segundo Encuentro de la Red Argentina de Bacterias Lácticas (Red- BAL); 2009
Institución organizadora:
Centro de Referencia para Lactobacilos (CERELA) - CONICET
Resumen:
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Up to date; many of the mechanisms of this effect remain unclear. On the other hand, the integrity of cholesterol-and sphingolipid-enriched microdomains, called membrane rafts, of eukaryotic cells was determined to be important for the bacteria-target cells interaction. We explored whether rafts disruption of human peripheral blood mononuclear cells (PBMC) could influence the effect of probiotic strain L. acidophilus CRL 1014 (L a 1014) on cellular cytokines production profile and which bacterial components were involved in involved in the bacteria-cells interaction. To disrupt rafts, PBMC were treated with 10 mM methyl-β-cyclodextrin (MβCD), a cholesterol extracting drug. Control and disrupted-lipid rafts cells (MβCD cells) were incubated with viable and heat killed L.a1014, conditioned media produced by live bacteria (L.a1014 CM), soluble bacterial surface component (L.a1014 SC) and disrupt bacteria (L.a1014 DB) obtained by sonication, in RPMI 1640 medium, at 37ºC and at different incubation times. TNF-α, IL-1β and IL-10 were detected in cell culture supernatants by ELISA. The results showed that live L.a1014 produced a stimulus of TNF-α and IL-1β production by control cells (86 and 35 times baseline values at 8 h of incubation). In case of TNF-α, similar effect was observed when PBMC were incubated with heat-killed bacteria; this stimulatory effect was decreased in MβCD cells by 69% of the control cells value. Heat-killed L.a1014 was less effective to stimulate IL-1β production at 4 hours (35% of viable