Department of Anatomy and Cell Biology, University of Illinois at Chicago, Chicago, Illinois 60612, USA.
J Neurosci. 2013 Jun 12;33(24):10048-56. doi: 10.1523/JNEUROSCI.0217-13.2013.
Loss of function of galactosylceramidase lysosomal activity causes demyelination and vulnerability of various neuronal populations in Krabbe disease. Psychosine, a lipid-raft-associated sphingolipid that accumulates in this disease, is thought to trigger these abnormalities. Myelin-free in vitro analyses showed that psychosine inhibited fast axonal transport through the activation of axonal PP1 and GSK3β in the axon. Abnormal levels of activated GSK3β and abnormally phosphorylated kinesin light chains were found in nerve samples from a mouse model of Krabbe disease. Administration of GSK3β inhibitors significantly ameliorated transport defects in vitro and in vivo in peripheral axons of the mutant mouse. This study identifies psychosine as a pathogenic sphingolipid able to block fast axonal transport and is the first to provide a molecular mechanism underlying dying-back degeneration in this genetic leukodystrophy.
半乳糖脑苷脂酶溶酶体活性丧失导致克拉伯病中各种神经元群体脱髓鞘和易损。神经醇胺,一种在这种疾病中积累的与脂筏相关的鞘脂,被认为引发了这些异常。无髓鞘的体外分析表明,神经醇胺通过激活轴突中的轴突 PP1 和 GSK3β 来抑制快速轴突运输。在克拉伯病小鼠模型的神经样本中发现了激活的 GSK3β 和异常磷酸化的驱动蛋白轻链的异常水平。GSK3β 抑制剂的给药显著改善了体外和体内突变小鼠周围轴突的运输缺陷。这项研究确定神经醇胺是一种能够阻断快速轴突运输的致病鞘脂,并首次提供了这种遗传性脑白质营养不良中退行性变的分子机制。