Aschner M, Cherian M G, Klaassen C D, Palmiter R D, Erickson J C, Bush A I
Department of Physiology and Pharmacology, Bowman Gray School of Medicine of Wake Forest University, Winston-Salem, North Carolina 27157-1083, USA.
Toxicol Appl Pharmacol. 1997 Feb;142(2):229-42. doi: 10.1006/taap.1996.8054.
A symposium on the role of brain metallothioneins (MTs) in physiology and pathology was held at the 1996 Annual Society of Toxicology Meeting in Anaheim, California. The objectives of this symposium were to: (1) review the physiologic function of MTs, (2) examine the distribution of brain MTs with particular emphasis on cell-specific localization (neurons vs neuroglia), (3) discuss MT gene responsiveness upon toxic insult with metals, and (4) discuss the potential role of MTs in the etiology of neurodegenerative disorders. Dr. Cherian discussed the biochemical properties of the MTs, emphasizing structural similarities and differences between the MTs. Dr. Klaassen addressed the expression and distribution of the MTs in brains with special reference to the cell-specific localization of MTs. Dr. Aschner provided data illustrating a potential role for MTs in attenuating the cytotoxicity caused by methylmercury (MeHg) in cultured neonatal astrocytes. Dr. Palmiter discussed the properties of MT-III and the increased sensitivity of MT-III knockout mice to kainate-induced seizures. Cerebral zinc metabolism, its relationship to MT homeostasis, and its pathogenic potential in Alzheimer's disease was addressed by Dr. Bush.
一场关于脑金属硫蛋白(MTs)在生理学和病理学中作用的研讨会于1996年在加利福尼亚州阿纳海姆举行的毒理学会年会上召开。本次研讨会的目标是:(1)回顾MTs的生理功能,(2)研究脑MTs的分布,特别强调细胞特异性定位(神经元与神经胶质细胞),(3)讨论MT基因对金属毒性损伤的反应,以及(4)讨论MTs在神经退行性疾病病因学中的潜在作用。切里安博士讨论了MTs的生化特性,强调了MTs之间的结构异同。克拉斯森博士阐述了MTs在脑中的表达和分布,特别提及了MTs的细胞特异性定位。阿斯chner博士提供的数据表明MTs在减轻培养的新生星形胶质细胞中甲基汞(MeHg)引起的细胞毒性方面具有潜在作用。帕尔米特博士讨论了MT-III的特性以及MT-III基因敲除小鼠对谷氨酸诱导的癫痫发作的敏感性增加。布什博士探讨了脑锌代谢、其与MT内稳态的关系以及在阿尔茨海默病中的致病潜力。