Rawji Khalil S, Neumann Björn, Franklin Robin J M
Altos Labs, Cambridge Institute of Science, Cambridge, UK.
Ann N Y Acad Sci. 2023 Jan;1519(1):34-45. doi: 10.1111/nyas.14933. Epub 2022 Nov 18.
Aging is a major risk factor for several neurodegenerative diseases and is associated with cognitive decline. In addition to affecting neuronal function, the aging process significantly affects the functional phenotype of the glial cell compartment, comprising oligodendrocyte lineage cells, astrocytes, and microglia. These changes result in a more inflammatory microenvironment, resulting in a condition that is favorable for neuron and synapse loss. In addition to facilitating neurodegeneration, the aging glial cell population has negative implications for central nervous system remyelination, a regenerative process that is of particular importance to the chronic demyelinating disease multiple sclerosis. This review will discuss the changes that occur with aging in the three main glial populations and provide an overview of the studies documenting the impact these changes have on remyelination.
衰老是多种神经退行性疾病的主要风险因素,与认知能力下降有关。除了影响神经元功能外,衰老过程还显著影响神经胶质细胞区室的功能表型,神经胶质细胞区室包括少突胶质细胞系细胞、星形胶质细胞和小胶质细胞。这些变化导致更具炎症性的微环境,从而形成有利于神经元和突触丧失的条件。衰老的神经胶质细胞群体除了促进神经退行性变外,还对中枢神经系统的髓鞘再生产生负面影响,髓鞘再生是一个对慢性脱髓鞘疾病多发性硬化症尤为重要的再生过程。本综述将讨论三种主要神经胶质细胞群体随衰老发生的变化,并概述记录这些变化对髓鞘再生影响的研究。