Immunocytochemical Localization of TASK-3 Channels in Rat Motor Neurons |
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Authors: | Christiane Marinc Harald Prüss Christian Derst Rüdiger W. Veh |
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Affiliation: | (1) Institut f?r Integrative Neuroanatomie, Charit?, Philippstr. 12, 10115 Berlin, Germany;(2) Department of Neurology and Experimental Neurology, Charit?, Charit?platz 1, 10117 Berlin, Germany;(3) Institut f?r Integrative Neuroanatomie, Centrum f?r Anatomie, Charit? - Universit?tsmedizin Berlin, 10115 Berlin, Germany; |
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Abstract: | Motor neurons are large cholinergic neurons located in the brain stem and spinal cord. In recent years, a functional role for TASK channels in cellular excitability and vulnerability to anesthetics of motor neurons has been described. Using a polyclonal monospecific antibody against the tandem pore domain K+ channel (K2P channel) TWIK-related acid-sensitive K+ channel (TASK-3), we analyzed the expression of the TASK-3 protein in motor systems of the rat CNS. Immunocytochemical staining showed strong TASK-3 expression in motor neurons of the facial, trigeminal, ambiguus, and hypoglossal nuclei. Oculomotor nuclei (including trochlear and abducens nucleus) were also strongly positive for TASK-3. The parasympathetic Edinger-Westphal nucleus and dorsal vagal nucleus showed significant, but weaker expression compared with somato- and branchiomotoric neurons. In addition, motor neurons in the anterior horn of the spinal cord were also strongly labeled for TASK-3 immunoreactivity. Based on morphological criteria, TASK-3 was found in the somatodendritic compartment of motor neurons. Cellular staining using methyl green and immunofluorescence double-labeling with anti-vesicular acetylcholine transporter (anti-vAChT) indicated ubiquitous TASK-3 expression in motor neurons, whereas in other brain regions TASK-3 showed a widespread but not ubiquitous expression. In situ hybridization using a TASK-3 specific riboprobe verified the expression of TASK-3 in motor neurons at the mRNA level. |
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