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Attila Miseta

Attila Miseta

University of Pécs,Hungary

Title: Hepcidin maturation: the possible role of alpha-1 antitrypsin

Biography

Biography: Attila Miseta

Abstract

Hepcidin is a 25AA peptide hormone made in the hepatocytes. The primary role of hepcidin is in the regulation of iron homeostasis. Similarly to many other peptide hormones it undergoes maturation meaning that the primary 84 AA product of the HAMP gene is cleaved to 60AA prohepcidin and subsequently to the 25 AA active compound. Both prohepcidin and hepcidin is present in circulation. In addition some shorter forms were also detected, 22 and 20AA long respectively. Furin type serine proteases are known to be responsible for the maturation/degradation of the primary peptide product. We used a bacterial two-hybrid system to identify possible significant interactions to uncover why there is so much prohepcidine in the serum. Screening assays were carried out on a human liver cDNA library. Preprohepcidin screening gave the following results: alpha-1 antitrypsin, transthyretin and alpha-1-acid glycoprotein showed strong interactions with preprohepcidin. We further confirmed and examined the alpha-1 antitrypsin binding in vitro (glutathione S-transferase, pull down, coimmunoprecipitation, MALDI-TOF) and in vivo (ELISA, cross-linking assay). Our results demonstrated that the serine protease inhibitor alpha-1 antitrypsin binds preprohepcidin within the cell during maturation. Furthermore, alpha-1 antitrypsin binds prohepcidin significantly in the plasma. This observation may explain the presence of prohormone in the circulation, as well as the post-translational regulation of the mature hormone level in the blood. In addition, the lack of cleavage protection in patients with alpha-1 antitrypsin deficiency may be the reason for the disturbance in their iron homeostasis.