Expression patterns of NKCC1 in neurons and non-neuronal cells during cortico-hippocampal development

被引:29
作者
Kurki, Samu N. [1 ,2 ]
Uvarov, Pavel [1 ,2 ]
Pospelov, Alexey S. [1 ,2 ]
Trontti, Kalevi [2 ,3 ,4 ]
Huebner, Antje K. [5 ]
Srinivasan, Rakenduvadhana [1 ,2 ]
Watanabe, Masahiko [6 ]
Hovatta, Iiris [2 ,3 ,4 ]
Huebner, Christian A. [5 ]
Kaila, Kai [1 ,2 ]
Virtanen, Mari A. [1 ,2 ]
机构
[1] Univ Helsinki, Mol & Integrat Biosci, Helsinki 00014, Finland
[2] Univ Helsinki, Neurosci Ctr, Helsinki Inst Life Sci, Helsinki 00014, Finland
[3] Univ Helsinki, Fac Med, SleepWell Res Program, Helsinki 00014, Finland
[4] Univ Helsinki, Dept Psychol & Logoped, Helsinki 00014, Finland
[5] Friedrich Schiller Univ, Inst Human Genet, Jena Univ Hosp, D-07747 Jena, Germany
[6] Hokkaido Univ, Fac Med, Dept Anat, Sapporo, Hokkaido 0608638, Japan
基金
芬兰科学院;
关键词
NKCC1; Slc12a2; chloride regulation; bumetanide; neurodevelopmental disorders; CATION-CHLORIDE COTRANSPORTERS; K-CL COTRANSPORTERS; NA-K-2CL COTRANSPORTER; GABA ACTIONS; NA+-K+-2CL(-) COTRANSPORTER; DIFFERENTIAL DISTRIBUTION; PHYSIOLOGICAL-FUNCTION; GLUTAMATE RELEASE; PYRAMIDAL NEURONS; BRAIN-DEVELOPMENT;
D O I
10.1093/cercor/bhac470
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The Na-K-2Cl cotransporter NKCC1 is widely expressed in cells within and outside the brain. However, our understanding of its roles in brain functions throughout development, as well as in neuropsychiatric and neurological disorders, has been severely hindered by the lack of reliable data on its developmental and (sub)cellular expression patterns. We provide here the first properly controlled analysis of NKCC1 protein expression in various cell types of the mouse brain using custom-made antibodies and an NKCC1 knock-out validated immunohistochemical procedure, with parallel data based on advanced mRNA approaches. NKCC1 protein and mRNA are expressed at remarkably high levels in oligodendrocytes. In immature neurons, NKCC1 protein was located in the somata, whereas in adult neurons, only NKCC1 mRNA could be clearly detected. NKCC1 immunoreactivity is also seen in microglia, astrocytes, developing pericytes, and in progenitor cells of the dentate gyrus. Finally, a differential expression of NKCC1 splice variants was observed, with NKCC1a predominating in non-neuronal cells and NKCC1b in neurons. Taken together, our data provide a cellular basis for understanding NKCC1 functions in the brain and enable the identification of major limitations and promises in the development of neuron-targeting NKCC1-blockers.
引用
收藏
页码:5906 / 5923
页数:18
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