Sterol metabolism regulates neuroserpin polymer degradation in the absence of the unfolded protein response in the dementia FENIB

Abstract

Mutants of neuroserpin are retainedas polymers within the endoplasmic reticulum (ER) of neurones to cause the autosomaldominantdementia familialencephalopathy with neuroserpin inclusionbodies or FENIB.Thecellular consequences are unusual in that the ordered polymers activate theERoverload response (EOR) in the absence of the canonical unfolded protein response. We use both cell lines and Drosophila models to show that the G392Emutant of neuroserpin thatforms polymers isdegradedbyUBE2j1E2ligaseandHrd1E3ligase while truncated neuroserpin, a protein that lacks 132 amino acids, is degraded by UBE2g2 (E2) and gp78 (E3) ligases. The degradation of G392E neuroserpin results from SREBP-dependent activation of the cholesterol biosynthetic pathway in cells that express polymers of neuroserpin (G392E). Inhibition of HMGCoA reductase, the limiting enzyme of the cholesterol biosynthetic pathway, reduced the ubiquitination of G392E neuroserpin in our cell lines and increased the retention of neuroserpin polymers in both HeLa cells and primary neurones. Our data reveal a reciprocal relationship between cholesterol biosynthesis and the clearance of mutant neuroserpin. This represents the first description of a link between sterol metabolism and modulation of the proteotoxicity mediated by the EOR.