2026-04-17T03:06:36Zhttps://recercat.cat/oai/request
oai:recercat.cat:2445/1293702025-12-05T09:21:31Zcom_2072_1057col_2072_478799col_2072_478916col_2072_478917col_2072_478929
RECERCAT author Hoegg-Beiler, Maja B. author Sirisi Dolcet, Sònia author Orozco, Ian J. author Ferrer, Isidro (Ferrer Abizanda) author Hohensee, Svea author Auberson, Muriel author Gödde, Kathrin author Vilches, Clara author López de Heredia, Miguel author Nunes Martínez, Virginia author Estévez Povedano, Raúl author Jentsch, Thomas J. 2019-02-28T12:51:05Z2019-02-28T12:51:05Z20142019-02-28T12:51:05Z Defects in the astrocytic membrane protein MLC1, the adhesion molecule GlialCAM or the chloride channel ClC-2 underlie human leukoencephalopathies. Whereas GlialCAM binds ClC-2 and MLC1, and modifies ClC-2 currents in vitro, no functional connections between MLC1 and ClC-2 are known. Here we investigate this by generating loss-of-function Glialcam and Mlc1 mouse models manifesting myelin vacuolization. We find that ClC-2 is unnecessary for MLC1 and GlialCAM localization in brain, whereas GlialCAM is important for targeting MLC1 and ClC-2 to specialized glial domains in vivo and for modifying ClC-2's biophysical properties specifically in oligodendrocytes (OLs), the cells chiefly affected by vacuolization. Unexpectedly, MLC1 is crucial for proper localization of GlialCAM and ClC-2, and for changing ClC-2 currents. Our data unmask an unforeseen functional relationship between MLC1 and ClC-2 in vivo, which is probably mediated by GlialCAM, and suggest that ClC-2 participates in the pathogenesis of megalencephalic leukoencephalopathy with subcortical cysts. cc-by (c) Hoegg-Beiler, Maja B. et al., 2014 http://creativecommons.org/licenses/by/3.0/es info:eu-repo/semantics/openAccess Malalties cerebrals Teixit nerviós Metabolisme cel·lular Proteïnes de membrana Canals de clorur Brain diseases Nerve tissue Cell metabolism Membrane proteins Chloride channels Disrupting MLC1 and GlialCAM and ClC-2interactions in leukodystrophy entails glial chloridechannel dysfunction info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion