The immunoproteasome is induced by cytokines and regulates apoptosis in human islets

In addition to degrading misfolded and damaged proteins, the proteasome regulates the fate of cells in response to stress. The role of the proteasome in pro-inflammatory cytokine-induced human beta-cell apoptosis is unknown. Using INS-1, INS-1E and human islets exposed to combinations of IFN, IL-1β and TNFα with or without addition of small molecules, we assessed the role of the immunoproteasome in pancreatic beta-cell demise. Here, we show that cytokines induce the expression and activity of the immuno-proteasome in INS-1E cells and human islets. Cytokine-induced expression of immuno-proteasome subunits, but not activity, depended upon histone deacetylase 3 activation. Inhibition of JAK1/STAT1 signaling did not affect proteasomal activity. Inhibition of the immuno-proteasome subunit PSMB8 aggravated cytokine-induced human beta-cell apoptosis while reducing intracellular levels of oxidized proteins in INS-1 cells. While cytokines increased total cellular NFB subunit P50 and P52 levels and reduced the cytosolic NFB subunit P65 and IB levels, these effects were unaffected by PSMB8 inhibition. We conclude that beta cells upregulate immuno-proteasome expression and activity in response to IFN, likely as a protective response to confine inflammatory signaling.

Source: Journal of Endocrinology - May 31, 2017 Category: Endocrinology Authors: Lundh, M., Bugliani, M., Dahlby, T., Chou, D. H.-C., Wagner, B., Ghiasi, S. M., De Tata, V., Chen, Z., Lund, M. N., Davies, M. J., Marchetti, P., Mandrup-Poulsen, T. Tags: Research Source Type: research