Heme Mediated STAT3 Activation in Severe MalariaReportar como inadecuado




Heme Mediated STAT3 Activation in Severe Malaria - Descarga este documento en PDF. Documentación en PDF para descargar gratis. Disponible también para leer online.

Background

The mortality of severe malaria cerebral malaria CM, severe malaria anemia SMA, acute lung injury ALI and acute respiratory distress syndrome ARDS remains high despite the availability associated with adequate treatments. Recent studies in our laboratory and others have revealed a hitherto unknown correlation between chemokine CXCL10-CXCR3, Heme-HO-1 and STAT3 and cerebral malaria severity and mortality. Although Heme-HO-1 and CXCL10-CXCR3 interactions are directly involved in the pathogenesis of CM and fatal disease, the mechanism dictating how Heme-HO-1 and CXCL10-CXCR3 are expressed and regulated under these conditions is still unknown. We therefore tested the hypothesis that these factors share common signaling pathways and may be mutually regulated.

Methods

We first clarified the roles of Heme-HO-1, CXCL10-CXCR3 and STAT3 in CM pathogenesis utilizing a well established experimental cerebral malaria mouse ECM, P. berghei ANKA model. Then, we further determined the mechanisms how STAT3 regulates HO-1 and CXCL10 as well as mutual regulation among them in CRL-2581, a murine endothelial cell line.

Results

The results demonstrate that 1 STAT3 is activated by P. berghei ANKA PBA infection in vivo and Heme in vitro. 2 Heme up-regulates HO-1 and CXCL10 production through STAT3 pathway, and regulates CXCL10 at the transcriptional level in vitro. 3 HO-1 transcription is positively regulated by CXCL10. 4 HO-1 regulates STAT3 signaling.

Conclusion

Our data indicate that Heme-HO-1, CXCL10-CXCR3 and STAT3 molecules as well as related signaling pathways play very important roles in the pathogenesis of severe malaria. We conclude that these factors are mutually regulated and provide new opportunities to develop potential novel therapeutic targets that could be used to supplement traditional prophylactics and treatments for malaria and improve clinical outcomes while reducing malaria mortality. Our ultimate goal is to develop novel therapies targeting Heme or CXCL10-related biological signaling molecules associated with development of fatal malaria.



Autor: Mingli Liu, Audu S. Amodu, Sidney Pitts, John Patrickson, Jacqueline M. Hibbert, Monica Battle, Solomon F. Ofori-Acquah, Jonathan

Fuente: http://plos.srce.hr/



DESCARGAR PDF




Documentos relacionados