摘要
Neurodegenerative disease is a condition in which subpopulations of neuronal cells of the brain and spinal cord are selectively lost. A common event in many neurodegenerative diseases, such as Parkinson＇s disease （PD）, Alzheimer＇s disease （AD）, amyotrophic lateral sclerosis （ALS）, multiple sclerosis and prion diseases, is the increased level of endoplasmic reticulum （ER） stress caused by accumulation and deposits of inclusion bodies that contain abnormal aggregated proteins. However, the exact contributions to and causal effects of ER stress in neuron degeneration are not clear （Lindholm et al., 2006）.
Neurodegenerative disease is a condition in which subpopulations of neuronal cells of the brain and spinal cord are selectively lost. A common event in many neurodegenerative diseases, such as Parkinson＇s disease （PD）, Alzheimer＇s disease （AD）, amyotrophic lateral sclerosis （ALS）, multiple sclerosis and prion diseases, is the increased level of endoplasmic reticulum （ER） stress caused by accumulation and deposits of inclusion bodies that contain abnormal aggregated proteins. However, the exact contributions to and causal effects of ER stress in neuron degeneration are not clear （Lindholm et al., 2006）.
基金
supported by the Paul and Harriett Campbell Fund for ALS Research
the Zimmerman Family Love Fund
the Judith&Jean Pape Adams Charitable Foundation
