4.4 Article

Subcellular compartmentalisation of copper, iron, manganese, and zinc in the Parkinson's disease brain

期刊

METALLOMICS
卷 9, 期 10, 页码 1447-1455

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7mt00244k

关键词

-

资金

  1. Victorian Government's Operational Infrastructure Support Program
  2. Parkinson's NSW
  3. University of Sydney (Biomedical Science, BRIG)
  4. National Health and Medical Research Council [1122981]
  5. National Health and Medical Research Council (Australia) [1079679]
  6. National Health and Medical Research Council of Australia
  7. Schizophrenia Research Institute
  8. National Institute of Alcohol Abuse and Alcoholism (NIH (NIAAA)) [R24AA012725]
  9. Sydney Brain Bank
  10. Neuroscience Research Australia
  11. University of New South Wales
  12. Agilent Technologies, GMH
  13. National Health and Medical Research Council of Australia [1122981] Funding Source: NHMRC

向作者/读者索取更多资源

Elevated iron and decreased copper levels are cardinal features of the degenerating substantia nigra pars compacta in the Parkinson's disease brain. Both of these redox-active metals, and fellow transition metals manganese and zinc, are found at high concentrations within the midbrain and participate in a range of unique biological reactions. We examined the total metal content and cellular compartmentalisation of manganese, iron, copper and zinc in the degenerating substantia nigra, disease-affected but non-degenerating fusiform gyrus, and unaffected occipital cortex in the post mortem Parkinson's disease brain compared with age-matched controls. An expected increase in iron and a decrease in copper concentration was isolated to the soluble cellular fraction, encompassing both interstitial and cytosolic metals and metal-binding proteins, rather than the membrane-associated or insoluble fractions. Manganese and zinc levels did not differ between experimental groups. Altered Fe and Cu levels were unrelated to Braak pathological staging in our cases of late stage (Braak stage V and VI) disease. The data supports our hypothesis that regional alterations in Fe and Cu, and in proteins that utilise these metals, contribute to the regional selectively of neuronal vulnerability in this disorder.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.4
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据