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  • Abundance of gap junctions at glutamatergic mixed synapses in adult Mosquitofish spinal cord neurons.

Abundance of gap junctions at glutamatergic mixed synapses in adult Mosquitofish spinal cord neurons.

Frontiers in neural circuits (2014-07-16)
Jose L Serrano-Velez, Melanie Rodriguez-Alvarado, Irma I Torres-Vazquez, Scott E Fraser, Thomas Yasumura, Kimberly G Vanderpool, John E Rash, Eduardo Rosa-Molinar
摘要

"Dye-coupling", whole-mount immunohistochemistry for gap junction channel protein connexin 35 (Cx35), and freeze-fracture replica immunogold labeling (FRIL) reveal an abundance of electrical synapses/gap junctions at glutamatergic mixed synapses in the 14th spinal segment that innervates the adult male gonopodium of Western Mosquitofish, Gambusia affinis (Mosquitofish). To study gap junctions' role in fast motor behavior, we used a minimally-invasive neural-tract-tracing technique to introduce gap junction-permeant or -impermeant dyes into deep muscles controlling the gonopodium of the adult male Mosquitofish, a teleost fish that rapidly transfers (complete in <20 mS) spermatozeugmata into the female reproductive tract. Dye-coupling in the 14th spinal segment controlling the gonopodium reveals coupling between motor neurons and a commissural primary ascending interneuron (CoPA IN) and shows that the 14th segment has an extensive and elaborate dendritic arbor and more gap junctions than do other segments. Whole-mount immunohistochemistry for Cx35 results confirm dye-coupling and show it occurs via gap junctions. Finally, FRIL shows that gap junctions are at mixed synapses and reveals that >50 of the 62 gap junctions at mixed synapses are in the 14th spinal segment. Our results support and extend studies showing gap junctions at mixed synapses in spinal cord segments involved in control of genital reflexes in rodents, and they suggest a link between mixed synapses and fast motor behavior. The findings provide a basis for studies of specific roles of spinal neurons in the generation/regulation of sex-specific behavior and for studies of gap junctions' role in regulating fast motor behavior. Finally, the CoPA IN provides a novel candidate neuron for future studies of gap junctions and neural control of fast motor behaviors.

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Sigma-Aldrich
乙酰化微管蛋白单克隆抗体 小鼠抗, clone 6-11B-1, ascites fluid
Sigma-Aldrich
抗连接蛋白35/36抗体,克隆8F6.2, clone 8F6.2, Chemicon®, from mouse
Sigma-Aldrich
Anti-Connexin 35/36 Antibody, clone 9D7.2, clone 9D7.2, Chemicon®, from mouse