Verkhratsky Alexei, Parpura Vladimir, Pekna Marcela, Pekny Milos, Sofroniew Michael
††Department of Neurobiology, University of California, Los Angeles, CA 90095, U.S.A.
Biochem Soc Trans. 2014 Oct;42(5):1291-301. doi: 10.1042/BST20140107.
Exclusively neuron-centric approaches to neuropathological mechanisms have not resulted in major new breakthroughs in the prevention and therapy of neurodegenerative diseases. In the present paper, we review the role of glia in neurodegeneration in an attempt to identify novel targets that could be used to develop much-needed strategies for the containment and cure of neurodegenerative disorders. We discuss this in the context of glial roles in the homoeostasis and defence of the brain. We consider the mounting evidence supporting a change away from the perception of reactive glial responses merely as secondary detrimental processes that exacerbate the course of neurological disorders, in favour of an emerging contemporary view of glial pathological responses as complex and multistaged defensive processes that also have the potential for dysfunction.
仅以神经元为中心研究神经病理机制的方法,在神经退行性疾病的预防和治疗方面尚未取得重大新突破。在本文中,我们回顾了胶质细胞在神经退行性变中的作用,试图确定新的靶点,用于制定遏制和治愈神经退行性疾病急需的策略。我们将在胶质细胞在大脑稳态和防御中的作用背景下进行讨论。我们认为,越来越多的证据支持,应摒弃将反应性胶质细胞反应仅仅视为加剧神经疾病进程的继发性有害过程的观念,转而支持一种新出现的当代观点,即胶质细胞病理反应是复杂的多阶段防御过程,也可能出现功能障碍。