Brain Glioma Center & Department of Neurosurgery, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China.
Department of Physiology, Wuhan University School of Basic Medical Sciences, Wuhan, Hubei, China.
Cell Mol Neurobiol. 2024 May 14;44(1):46. doi: 10.1007/s10571-024-01481-6.
Central nervous system (CNS) disorders represent the leading cause of disability and the second leading cause of death worldwide, and impose a substantial economic burden on society. In recent years, emerging evidence has found that beta2 -microglobulin (B2M), a subunit of major histocompatibility complex class I (MHC-I) molecules, plays a crucial role in the development and progression in certain CNS diseases. On the one hand, intracellular B2M was abnormally upregulated in brain tumors and regulated tumor microenvironments and progression. On the other hand, soluble B2M was also elevated and involved in pathological stages in CNS diseases. Targeted B2M therapy has shown promising outcomes in specific CNS diseases. In this review, we provide a comprehensive summary and discussion of recent advances in understanding the pathological processes involving B2M in CNS diseases (e.g., Alzheimer's disease, aging, stroke, HIV-related dementia, glioma, and primary central nervous system lymphoma).
中枢神经系统(CNS)疾病是全球范围内导致残疾和死亡的主要原因,给社会带来了巨大的经济负担。近年来,新出现的证据表明,β2-微球蛋白(B2M)是主要组织相容性复合体 I 类(MHC-I)分子的亚基,在某些中枢神经系统疾病的发展和进展中起着至关重要的作用。一方面,脑肿瘤中细胞内 B2M 异常上调,调节肿瘤微环境和进展。另一方面,可溶性 B2M 也升高,并参与中枢神经系统疾病的病理阶段。针对 B2M 的治疗在特定的中枢神经系统疾病中显示出有前景的结果。在这篇综述中,我们对中枢神经系统疾病中涉及 B2M 的病理过程的最新进展进行了全面的总结和讨论(例如,阿尔茨海默病、衰老、中风、HIV 相关痴呆、神经胶质瘤和原发性中枢神经系统淋巴瘤)。