Recombinant human prolactin promotes human beta cell survival via inhibition of extrinsic and intrinsic apoptosis pathways

• DOI: 10.1007/s00125-011-2102-z
• Publication Date: 2011-03-10T09:21:12Z
• Authors: L. F. Terra; M. H. Garay-Malpa...; R. A. M. Wailemann; M. C. Sogayar; L. Labriola
• Keywords: Adult; 0303 health sciences; Cell Survival; Islets of Langerhans Transplantation; Apoptosis; Middle Aged; Caspase Inhibitors; Recombinant Proteins; Prolactin; 3. Good health; 03 medical and health sciences; Diabetes Mellitus, Type 1; Proto-Oncogene Proteins c-bcl-2; Insulin-Secreting Cells; Cytokines; Humans; Cells, Cultured; Signal Transduction; bcl-2-Associated X Protein

Transplantation of pancreatic islets constitutes a promising alternative treatment for type 1 diabetes. However, it is limited by the shortage of organ donors. Previous results from our laboratory have demonstrated beneficial effects of recombinant human prolactin (rhPRL) treatment on beta cell cultures. We therefore investigated the role of rhPRL action in human beta cell survival, focusing on the molecular mechanisms involved in this process.Human pancreatic islets were isolated using an automated method. Islet cultures were pre-treated in the absence or presence of rhPRL and then subjected to serum starvation or cytokine treatment. Beta cells were labelled with Newport green and apoptosis was evaluated using flow cytometry analysis. Levels of BCL2 gene family members were studied by quantitative RT-PCR and western blot. Caspase-8, -9 and -3 activity, as well as nitric oxide production, were evaluated by fluorimetric assays.The proportion of apoptotic beta cells was significantly lowered in the presence of rhPRL under both cell death-induced conditions. We also demonstrated that cytoprotection may involve an increase of BCL2/BAX ratio, as well as inhibition of caspase-8, -9 and -3.Our study provides relevant evidence for a protective effect of lactogens on human beta cell apoptosis. The results also suggest that the improvement of cell survival may involve, at least in part, inhibition of cell death pathways controlled by the BCL2 gene family members. These findings are highly relevant for improvement of the islet isolation procedure and for clinical islet transplantation.