Heterogeneous Expression of the Potassium-Chloride Cotransporter KCC2 in Gonadotropin-Releasing Hormone Neurons of the Adult Mouse
Author(s) -
Sarah Leupen,
Stuart A. Tobet,
W F Crowley,
Kai Kaila
Publication year - 2003
Publication title -
endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.674
H-Index - 257
eISSN - 1945-7170
pISSN - 0013-7227
DOI - 10.1210/en.2002-220995
Subject(s) - colocalization , medicine , endocrinology , depolarization , cotransporter , supraoptic nucleus , gabaa receptor , excitatory postsynaptic potential , hyperpolarization (physics) , biology , receptor , gonadotropin releasing hormone , vasopressin , chemistry , hormone , inhibitory postsynaptic potential , neuroscience , luteinizing hormone , sodium , organic chemistry , nuclear magnetic resonance spectroscopy
In mature central neurons, chloride extrusion mediated by the K-Cl cotransporter KCC2 appears to be largely responsible for the Cl(-) driving force that allows gamma-aminobutyric acid(A) (GABA(A)) receptor activation to trigger a hyperpolarization. In its absence, GABA's effect is typically depolarizing and often excitatory. We examined the colocalization of KCC2 and GnRH in adult male and female mice using a combined in situ hybridization-immunofluorescence procedure. We found that KCC2 was localized to approximately 34% of GnRH neurons. This proportion was similar in females and males. However, females exhibited a marked rostrocaudal gradient of colocalization that was not seen in males. By contrast, KCC2 was localized to nearly all vasopressin neurons of the supraoptic nucleus. These results indicate that a substantial fraction of GnRH neurons may be depolarized and excited by GABA(A) receptor activation throughout life, supporting the existence of functionally heterogeneous subpopulations.
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