Distribution of the Creatine Transporter Throughout the Human Brain Reveals a Spectrum of Creatine Transporter Immunoreactivity

被引:37
|
作者
Lowe, Matthew T. J. [1 ,2 ]
Faull, Richard L. M. [1 ,2 ]
Christie, David L. [1 ,2 ,3 ]
Waldvogel, Henry J. [1 ,2 ]
机构
[1] Univ Auckland, Ctr Brain Res, Fac Med & Hlth Sci, Auckland 1142, New Zealand
[2] Univ Auckland, Dept Anat Radiol, Fac Med & Hlth Sci, Auckland 1142, New Zealand
[3] Univ Auckland, Sch Biol Sci, Auckland 1142, New Zealand
关键词
neuroenergetics; neurodegeneration; phosphocreatine; AB_10000347; AB_10000343; AB_10000342; AB_477010; AB_887872; AB_10123643; AB_2157554; AB_2114471; AB_2224402; IN-SITU; MONOCLONAL-ANTIBODY; PROTEIN-CONTENT; ENERGY BUDGET; RAT-BRAIN; EXPRESSION; KINASE; GAMT; MITOCHONDRIAL; LOCALIZATION;
D O I
10.1002/cne.23667
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Creatine is a molecule that supports energy metabolism in cells. It is carried across the plasma membrane by the creatine transporter. There has been recent interest in creatine for its neuroprotective effects in neurodegenerative diseases and its potential as a therapeutic agent. This study represents the first systematic investigation of the distribution of the creatine transporter in the human brain. We have used immunohistochemical techniques to map out its location and the intensity of staining. The transporter was found to be strongly expressed, especially in the large projection neurons of the brain and spinal cord. These include the pyramidal neurons in the cerebral cortex, Purkinje cells in the cerebellar cortex, and motor neurons of the somatic motor and visceromotor cranial nerve nuclei and the ventral horn of the spinal cord. Many other neurons in the brain also had some degree of creatine transporter immunoreactivity. By contrast, the medium spiny neurons of the striatum and the catecholaminergic neurons of the substantia nigra and locus coeruleus, which are implicated in neurodegenerative diseases, showed a very low to almost absent level of immunoreactivity for the transporter. We propose that the distribution may reflect the energy consumption by different cell types and that the extent of creatine transporter expression is proportional to the cell's energy requirements. Furthermore, the distribution indicates that supplemented creatine would be widely taken up by brain cells, although possibly less by those cells that degenerate in Huntington's and Parkinson's diseases. J. Comp. Neurol. 523:699-725, 2015. (c) 2014 Wiley Periodicals, Inc.
引用
收藏
页码:699 / 725
页数:27
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