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

Author:

Kurki Samu N12,Uvarov Pavel12,Pospelov Alexey S12,Trontti Kalevi234,Hübner Antje K5,Srinivasan Rakenduvadhana12,Watanabe Masahiko6,Hovatta Iiris234,Hübner Christian A5,Kaila Kai12,Virtanen Mari A12

Affiliation:

1. University of Helsinki Molecular and Integrative Biosciences, , 00014 Helsinki , Finland

2. Helsinki Institute of Life Science, University of Helsinki Neuroscience Center, , 00014 Helsinki , Finland

3. University of Helsinki SleepWell Research Program, Faculty of Medicine, , 00014 Helsinki , Finland

4. University of Helsinki Department of Psychology and Logopedics, , 00014 Helsinki , Finland

5. Jena University Hospital, Friedrich Schiller Universität Institute of Human Genetics, , 07747 Jena , Germany

6. Hokkaido University Department of Anatomy, Faculty of Medicine, , Sapporo 060–8638 , Japan

Abstract

Abstract 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.

Funder

BMBF

Finnish Medical Foundation

Emil Aaltonen Foundation

Academy of Finland

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience

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