Horning Kyle J, Caito Samuel W, Tipps K Grace, Bowman Aaron B, Aschner Michael
Department of Neurology, Vanderbilt University, Nashville, Tennessee 37232; email:
Annu Rev Nutr. 2015;35:71-108. doi: 10.1146/annurev-nutr-071714-034419. Epub 2015 May 13.
The understanding of manganese (Mn) biology, in particular its cellular regulation and role in neurological disease, is an area of expanding interest. Mn is an essential micronutrient that is required for the activity of a diverse set of enzymatic proteins (e.g., arginase and glutamine synthase). Although necessary for life, Mn is toxic in excess. Thus, maintaining appropriate levels of intracellular Mn is critical. Unlike other essential metals, cell-level homeostatic mechanisms of Mn have not been identified. In this review, we discuss common forms of Mn exposure, absorption, and transport via regulated uptake/exchange at the gut and blood-brain barrier and via biliary excretion. We present the current understanding of cellular uptake and efflux as well as subcellular storage and transport of Mn. In addition, we highlight the Mn-dependent and Mn-responsive pathways implicated in the growing evidence of its role in Parkinson's disease and Huntington's disease. We conclude with suggestions for future focuses of Mn health-related research.
对锰(Mn)生物学的理解,尤其是其细胞调节以及在神经疾病中的作用,是一个越来越受关注的领域。锰是一种必需的微量营养素,多种酶蛋白(如精氨酸酶和谷氨酰胺合成酶)的活性都需要它。尽管锰对生命至关重要,但过量时具有毒性。因此,维持细胞内锰的适当水平至关重要。与其他必需金属不同,尚未确定锰在细胞水平的稳态机制。在本综述中,我们讨论了锰暴露、吸收和运输的常见形式,包括通过肠道和血脑屏障的调节性摄取/交换以及通过胆汁排泄。我们介绍了目前对锰的细胞摄取和外排以及亚细胞储存和运输的理解。此外,我们强调了锰依赖和锰反应途径,这些途径在越来越多的证据表明其在帕金森病和亨廷顿病中的作用中有所涉及。我们最后提出了与锰健康相关研究未来重点的建议。