{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,30]],"date-time":"2026-09-30T16:20:22Z","timestamp":1790785222912,"version":"4.1.0"},"reference-count":42,"publisher":"Society for Neuroscience","issue":"45","license":[{"start":{"date-parts":[[2007,5,8]],"date-time":"2007-05-08T00:00:00Z","timestamp":1178582400000},"content-version":"vor","delay-in-days":181,"URL":"https:\/\/creativecommons.org\/licenses\/by-nc-sa\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J. Neurosci."],"published-print":{"date-parts":[[2006,11,8]]},"abstract":"<jats:p>Missense mutations in the human<jats:italic>PLP1<\/jats:italic>gene lead to dysmyelinating diseases with a broad range of clinical severity, ranging from severe Pelizaeus\u2013Merzbacher disease (PMD) to milder spastic paraplegia type 2 (SPG-2). The molecular pathology has been generally attributed to endoplasmic reticulum (ER) retention of misfolded proteolipid protein (PLP) (and its splice isoform DM20) and induction of the unfolded protein response. As opposed to previous studies of heterologous expression systems, we have analyzed PLP\/DM20 trafficking in oligodendroglial cells, thereby revealing differences between PMD and SPG-2-associated PLP\/DM20 isoforms. PLP<jats:sup>A242V<\/jats:sup>and DM20<jats:sup>A242V<\/jats:sup>(<jats:italic>jimpy-msd<\/jats:italic>in mice), associated with severe PMD-like phenotype<jats:italic>in vivo<\/jats:italic>, were not only retained in the ER but also interfered with oligodendroglial process formation. In contrast, glial cells expressing SPG-2-associated PLP<jats:sup>I186T<\/jats:sup>or DM20<jats:sup>I186T<\/jats:sup>(<jats:italic>rumpshaker<\/jats:italic>in mice) developed processes, and mutant PLP\/DM20 reached a late endosomal\/lysosomal compartment. Unexpectedly, PLP\/DM20 with either substitution exhibited impaired cholesterol binding, and the association with lipid raft microdomains was strongly reduced. Turnover analysis demonstrated that mutant PLP was rapidly degraded in oligodendroglial cells, with half-lives for PLP &gt; PLP<jats:sup>I186T<\/jats:sup>&gt; PLP<jats:sup>A242V<\/jats:sup>. Protein degradation was specifically sensitive to proteasome inhibition, although PLP\/DM20<jats:sup>I186T<\/jats:sup>degradation was also affected by inhibition of lysosomal enzymes. We conclude that, in addition to ER retention and unfolded protein response (UPR) induction, impaired cholesterol binding and lipid raft association are characteristic cellular defects of<jats:italic>PLP1<\/jats:italic>-missense mutations. Mutant protein is rapidly cleared and does not accumulate in oligodendroglial cells. Whereas UPR-induced cell death governs the PMD phenotype of the<jats:italic>msd<\/jats:italic>mutation, we propose that impaired cholesterol and lipid raft interaction of the<jats:italic>rsh<\/jats:italic>protein may contribute to the dysmyelination observed in SPG-2.<\/jats:p>","DOI":"10.1523\/jneurosci.3581-06.2006","type":"journal-article","created":{"date-parts":[[2006,11,8]],"date-time":"2006-11-08T17:18:09Z","timestamp":1163006289000},"page":"11743-11752","source":"Crossref","is-referenced-by-count":75,"title":["Perturbed Interactions of Mutant Proteolipid Protein\/DM20 with Cholesterol and Lipid Rafts in Oligodendroglia: Implications for Dysmyelination in Spastic 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