Laboratorio de Neurobiología Celular y Molecular, Unidad Académica de Histología y Embriología, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay.
Departamento de Neurobiología y Neuropatología, Instituto de Investigaciones Biológicas Clemente Estable (IIBCE), Montevideo, Uruguay.
Neurotox Res. 2024 Jul 4;42(4):33. doi: 10.1007/s12640-024-00710-6.
The white matter is an important constituent of the central nervous system, containing axons, oligodendrocytes, and its progenitor cells, astrocytes, and microglial cells. Oligodendrocytes are central for myelin synthesis, the insulating envelope that protects axons and allows normal neural conduction. Both, oligodendrocytes and myelin, are highly vulnerable to toxic factors in many neurodevelopmental and neurodegenerative disorders associated with disturbances of myelination. Here we review the main alterations in oligodendrocytes and myelin observed in some organic acidurias/acidemias, which correspond to inherited neurometabolic disorders biochemically characterized by accumulation of potentially neurotoxic organic acids and their derivatives. The yet incompletely understood mechanisms underlying the high vulnerability of OLs and/or myelin in glutaric acidemia type I, the most prototypical cerebral organic aciduria, are particularly discussed.
白质是中枢神经系统的重要组成部分,包含轴突、少突胶质细胞及其前体细胞、星形胶质细胞和小胶质细胞。少突胶质细胞是髓鞘合成的关键,髓鞘是一种保护轴突并允许正常神经传导的绝缘包膜。在许多与髓鞘形成障碍相关的神经发育和神经退行性疾病中,少突胶质细胞和髓鞘都极易受到有毒因素的影响。在这里,我们综述了一些有机酸血症/酸血症中观察到的少突胶质细胞和髓鞘的主要变化,这些疾病对应于遗传性神经代谢紊乱,其生化特征是潜在神经毒性有机酸及其衍生物的积累。特别讨论了在最典型的脑有机酸尿症——Ⅰ型戊二酸血症中,少突胶质细胞和/或髓鞘高度易损的潜在机制,这一机制尚未完全阐明。