Van Den Bosch L, Robberecht W
Neurobiology, K.U.Leuven, Campus Gasthuisberg O&N2, Herestraat 49, Leuven, Belgium.
Exp Neurol. 2008 May;211(1):1-6. doi: 10.1016/j.expneurol.2008.01.008. Epub 2008 Jan 26.
Motor neuron death as seen in amyotrophic lateral sclerosis (ALS) is likely to be a non-cell autonomous process. One cell type that may be involved in the pathogenesis of the disease is the astrocyte. Under normal conditions, astrocytes affect survival of motor neurons by releasing growth factors and removing glutamate from the synaptic cleft. In addition, they determine some of the functional characteristics of motor neurons. In turn, motor neurons affect the functional characteristics of astrocytes. Recent evidence suggests that activation of astrocytes in a degenerative disease like ALS leads to a disturbance of this crosstalk between astrocytes and motor neurons, and that this may contribute to the death of motor neurons. As a consequence, understanding the interactions between motor neurons and astrocytes in health and disease may have important therapeutic implications.
在肌萎缩侧索硬化症(ALS)中所见的运动神经元死亡很可能是一个非细胞自主过程。可能参与该疾病发病机制的一种细胞类型是星形胶质细胞。在正常情况下,星形胶质细胞通过释放生长因子和从突触间隙清除谷氨酸来影响运动神经元的存活。此外,它们还决定了运动神经元的一些功能特性。反过来,运动神经元也会影响星形胶质细胞的功能特性。最近的证据表明,在像ALS这样的退行性疾病中,星形胶质细胞的激活会导致星形胶质细胞与运动神经元之间这种相互作用的紊乱,而这可能导致运动神经元的死亡。因此,了解健康和疾病状态下运动神经元与星形胶质细胞之间的相互作用可能具有重要的治疗意义。