{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,13]],"date-time":"2026-10-13T02:50:27Z","timestamp":1791859827062,"version":"4.3.4"},"reference-count":513,"publisher":"MDPI AG","issue":"5","license":[{"start":{"date-parts":[[2025,5,17]],"date-time":"2025-05-17T00:00:00Z","timestamp":1747440000000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"name":"GETDOC (Groupe d\u2019Etude et de Th\u00e9rapeutique pour le Diab\u00e8te, l\u2019Ob\u00e9sit\u00e9, la Croissance) Association","award":["24\/25-01"],"award-info":[{"award-number":["24\/25-01"]}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Genes"],"abstract":"<jats:p>Background: X-ALD is a white matter (WM) disease caused by mutations in the ABCD1 gene encoding the transporter of very-long-chain fatty acids (VLCFAs) into peroxisomes. Strikingly, the same ABCD1 mutation causes either devastating brain inflammatory demyelination during childhood or, more often, progressive spinal cord axonopathy starting in middle-aged adults. The accumulation of undegraded VLCFA in glial cell membranes and myelin has long been thought to be the central mechanism of X-ALD. Methods: This review discusses studies in mouse and drosophila models that have modified our views of X-ALD pathogenesis. Results: In the Abcd1 knockout (KO) mouse that mimics the spinal cord disease, the late manifestations of axonopathy are rapidly reversed by ABCD1 gene transfer into spinal cord oligodendrocytes (OLs). In a peroxin-5 KO mouse model, the selective impairment of peroxisomal biogenesis in OLs achieves an almost perfect phenocopy of cerebral ALD. A drosophila knockout model revealed that VLCFA accumulation in glial myelinating cells causes the production of a toxic lipid able to poison axons and activate inflammatory cells. Other mouse models showed the critical role of OLs in providing energy substrates to axons. In addition, studies on microglial changing substates have improved our understanding of neuroinflammation. Conclusions: Animal models supporting a primary role of OLs and axonal pathology and a secondary role of microglia allow us to revisit of X-ALD mechanisms. Beyond ABCD1 mutations, pathogenesis depends on unidentified contributors, such as genetic background, cell-specific epigenomics, potential environmental triggers, and stochasticity of crosstalk between multiple cell types among billions of glial cells and neurons.<\/jats:p>","DOI":"10.3390\/genes16050590","type":"journal-article","created":{"date-parts":[[2025,5,20]],"date-time":"2025-05-20T04:48:18Z","timestamp":1747716498000},"page":"590","update-policy":"https:\/\/doi.org\/10.3390\/mdpi_crossmark_policy","source":"Crossref","is-referenced-by-count":11,"title":["Revisiting the Pathogenesis of X-Linked Adrenoleukodystrophy"],"prefix":"10.3390","volume":"16","author":[{"given":"Pierre","family":"Bougn\u00e8res","sequence":"first","affiliation":[{"name":"MIRCen Institute, Commissariat \u00e0 l\u2019Energie Atomique, Laboratoire des Maladies Neurod\u00e9g\u00e9n\u00e9ratives, 92260 Fontenay-aux-Roses, France"},{"name":"NEURATRIS, 92260 Fontenay-aux-Roses, France"},{"name":"Therapy Design Consulting, 94300 Vincennes, France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Catherine","family":"Le Stunff","sequence":"additional","affiliation":[{"name":"MIRCen Institute, Commissariat \u00e0 l\u2019Energie Atomique, Laboratoire des Maladies Neurod\u00e9g\u00e9n\u00e9ratives, 92260 Fontenay-aux-Roses, France"},{"name":"NEURATRIS, 92260 Fontenay-aux-Roses, France"},{"name":"UMR1195 Inserm, University Paris Saclay, 94270 Le Kremlin-Bic\u00eatre, France"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"1968","published-online":{"date-parts":[[2025,5,17]]},"reference":[{"key":"ref_1","doi-asserted-by":"crossref","unstructured":"Gaviglio, A., McKasson, S., Singh, S., and Ojodu, J. 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