Zhou Dan, Lin Yumeng, Han Zhongyu, Zhang Zhuyun, Lin Le, Lin Shichong, Yang Qianke
Department of Physical Medicine and Rehabilitation, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Zhejiang, China.
School of Smart Health Care (School of Health & Medical), Zhejiang Dongfang Polytechnic, Zhejiang, China.
Aging Dis. 2024 Nov 5;16(5):2953-2978. doi: 10.14336/AD.2024.1085.
With the progression of global aging, neurological diseases in elderly individuals have aroused widespread interest among researchers. Imbalances in the homeostasis of neuronal microenvironments, including neural progenitor cells and microglia, are the leading cause of worsening neurodegenerative diseases. The aging of various glial cells can further lead to abnormal functions in the central nervous system (CNS). Recent studies have shown that aging plays a vital role in a variety of degenerative diseases, including Huntington's disease (HD). In this manuscript, we describe the molecular mechanisms of aging, the cellular constitution of the neural microenvironment and the progression of aging in various neurodegenerative diseases, providing new targets and perspectives for the clinical treatment of various neurodegenerative diseases.
随着全球老龄化进程的推进,老年个体的神经系统疾病引起了研究人员的广泛关注。神经元微环境(包括神经祖细胞和小胶质细胞)稳态的失衡是神经退行性疾病恶化的主要原因。各种胶质细胞的老化会进一步导致中枢神经系统(CNS)功能异常。最近的研究表明,衰老在包括亨廷顿舞蹈症(HD)在内的多种退行性疾病中起着至关重要的作用。在本手稿中,我们描述了衰老的分子机制、神经微环境的细胞组成以及各种神经退行性疾病中衰老的进展,为各种神经退行性疾病的临床治疗提供了新的靶点和视角。