RESUMO
BACKGROUND: Toll-like receptor 4 (TLR4) is widely recognized as an essential element in the triggering of innate immunity, binding pathogen-associated molecules such as Lipopolysaccharide (LPS), and in initiating a cascade of pro-inflammatory events. Evidence for TLR4 expression in non-immune cells, including pancreatic ß-cells, has been shown, but, the functional role of TLR4 in the physiology of human pancreatic ß-cells is still to be clearly established. We investigated whether TLR4 is present in ß-cells purified from freshly isolated human islets and confirmed the results using MIN6 mouse insulinoma cells, by analyzing the effects of TLR4 expression on cell viability and insulin homeostasis. RESULTS: CD11b positive macrophages were practically absent from isolated human islets obtained from non-diabetic brain-dead donors, and TLR4 mRNA and cell surface expression were restricted to ß-cells. A significant loss of cell viability was observed in these ß-cells indicating a possible relationship with TLR4 expression. Monitoring gene expression in ß-cells exposed for 48h to the prototypical TLR4 ligand LPS showed a concentration-dependent increase in TLR4 and CD14 transcripts and decreased insulin content and secretion. TLR4-positive MIN6 cells were also LPS-responsive, increasing TLR4 and CD14 mRNA levels and decreasing cell viability and insulin content. CONCLUSIONS: Taken together, our data indicate a novel function for TLR4 as a molecule capable of altering homeostasis of pancreatic ß-cells.