Ettle Benjamin, Schlachetzki Johannes C M, Winkler Jürgen
Department of Molecular Neurology, Friedrich-Alexander University Erlangen-Nürnberg, Schwabachanlage 6, D-91054, Erlangen, Germany.
Mol Neurobiol. 2016 Jul;53(5):3046-3062. doi: 10.1007/s12035-015-9205-3. Epub 2015 May 13.
Oligodendrocytes, the myelinating cells of the central nervous system, mediate rapid action potential conduction and provide trophic support for axonal as well as neuronal maintenance. Their progenitor cell population is widely distributed in the adult brain and represents a permanent cellular reservoir for oligodendrocyte replacement and myelin plasticity. The recognition of oligodendrocytes, their progeny, and myelin as contributing factors for the pathogenesis and the progression of neurodegenerative disease has recently evolved shaping our understanding of these disorders. In the present review, we aim to highlight studies on oligodendrocytes and their progenitors in neurodegenerative diseases. We dissect oligodendroglial biology and illustrate evolutionary aspects in regard to their importance for neuronal functionality and maintenance of neuronal circuitries. After covering recent studies on oligodendroglia in different neurodegenerative diseases mainly in view of their function as myelinating cells, we focus on the alpha-synucleinopathy multiple system atrophy, a prototypical disorder with a well-defined oligodendroglial pathology.
少突胶质细胞是中枢神经系统的髓鞘形成细胞,介导快速动作电位传导,并为轴突以及神经元的维持提供营养支持。它们的祖细胞群体广泛分布于成人大脑中,是少突胶质细胞替代和髓鞘可塑性的永久细胞库。近年来,人们逐渐认识到少突胶质细胞、其后代以及髓鞘是神经退行性疾病发病机制和进展的促成因素,这改变了我们对这些疾病的理解。在本综述中,我们旨在突出关于神经退行性疾病中少突胶质细胞及其祖细胞的研究。我们剖析少突胶质细胞生物学,并阐述其在神经元功能和神经回路维持方面的重要性的进化方面。在主要从其作为髓鞘形成细胞的功能角度涵盖了不同神经退行性疾病中少突胶质细胞的近期研究之后,我们将重点关注α-突触核蛋白病多系统萎缩,这是一种具有明确少突胶质细胞病理学特征的典型疾病。